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#22716 From: "atkissonr" <robert1954@...>
Date: Sat Sep 1, 2007 2:11 am
Subject: Hemaglobin levels
atkissonr
Offline Offline
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Need some help here, can anyone give me some clues about a extremely
high Hemaglobin level.I went for my 6 month checkup monday and did lab
work and the doctor called today and said I had a very high hemaglobin
level, and wanted me to have the test run over again today, to see if
this is a possible error in the test.Ive never had any problems with
this before.Can anyone tell me what this possibly means if the test is
accurate.I wont know
  anything till at least sometime tuesday now.would appreciate some
answers her.Thanks  Rob

#22715 From: PoWeRTX@...
Date: Fri Aug 31, 2007 6:20 pm
Subject: AIDS drug shows potential as weapon against cancer
nelsonvergel
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AIDS drug shows potential as weapon against cancer

Fri Aug 31, 2007 5:12AM BST
 

WASHINGTON (Reuters) - A drug used to treat people infected with the AIDS virus has shown promise as a possible future weapon against cancer, U.S. researchers said on Friday.

Scientists at the U.S. National Cancer Institute examined how drugs called protease inhibitors, usually given in combination with other drugs to fight the human immunodeficiency virus, or HIV, performed against several types of cancer including non-small cell lung cancer.

In a study published in the journal Clinical Cancer Research, the scientists tested whether protease inhibitors would slow cancer cell growth in the laboratory and in mice. Three of six drugs they tried inhibited cancer cell growth.

The most effective of the drugs was nelfinavir, sold by Roche Holding AG as Viracept, the researchers said. The drug also slowed the growth of both drug-sensitive and drug-resistant breast cancer cells, they added.

The researchers have started an initial clinical trial to test nelfinavir in cancer patients.

Viracept won marketing approval in Europe in 1998. It was cleared for use a year earlier in the United States, where it is sold by Pfizer Inc..

The two other protease inhibitors that inhibited growth of cancer cells were ritonavir, sold by Abbott Laboratories Inc as Norvir, and saquinavir, sold by Roche as Invirase.

The researchers examined protease inhibitors because they affect a protein involved in the development of many cancer types. In people with HIV, such drugs can slow the spread of the virus in the body and reduce the risk of developing AIDS-related illnesses.

 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





Get a sneak peek of the all-new AOL.com.

#22714 From: PoWeRTX@...
Date: Fri Aug 31, 2007 6:17 pm
Subject: Eternal Sunset
nelsonvergel
Offline Offline
Send Email Send Email
 
Yes, I know.. I am sending another off topic email.. but I could not resist. This is way too cool and relaxing...

Eternal Sunset is a website that tracks 250 webcams across 49 countries. At any given time, the sun’s setting somewhere, and Eternal Sunset will show it to you.

It won’t add hours to your day (quite the contrary) but if you’ve always dreamed of seeing the perfect sunset in Napoli, Egypt, or from atop Mount Fuji, park yourself in front of your ‘puter and watch that fiery globe fall. Over and over again.

Cick here

Eternal Sunset

 

 

Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





Get a sneak peek of the all-new AOL.com.

#22713 From: "Mike W" <mwonders@...>
Date: Fri Aug 31, 2007 9:52 pm
Subject: No Fee Yoga of the BREATH Sept 14-21 San Francisco
sfmyke
Offline Offline
Send Email Send Email
 
Yoga of the Breath for People Living with HIV  Sept 14-21, 2007

Quan Yin Healing Arts Center (QYHAC) will host a no-fee 8 day Yoga of
the Breath course by the Art of Living from Friday Setember  14 -
Friday September 21 , 2007. Weekday sessions are from 7PM - 9:30PM
(except the start is 7:30PM Tue & Wed). Saturday & Sunday are 10AM -
2PM. All classes take place in QYHAC's classroom at 455 Valencia near
16 th Street.



  What is Yoga of the Breath? The cornerstone of the course is a
profound breathing technique, the Sudarshan Kriya that releases
stress, supports immune function and increases awareness. The course
includes instructions and processes which offer insights into the
many habits of the mind that contribute to stress and detract from or
quality life. By the end of the course, participants will be able to
practice these techniques at home on their on and join other
participants for ongoing weekly follow-up sessions at QYHAC. Each
class builds on the previous day so it is important that participants
be able to attend all 8 days.
Comments from previous courses:

"This workshop exceeded my expectations. It was the best gift that I
have given to myself in years."

"It was probably the most helpful thing I've ever done."

"It gave me peace of mind that I've never experienced before."



Contact  mwonders@... for a registration form or more
information.

Registration forms are also available at QYHAC's front desk (415-861-
4964). Class size is limited.

For a calendar of events, classes or more information you can visit
quanyinhealingartscenter.org and artoflivingsfba.org

An additional course will be held November 30-Dec7, 2007

#22712 From: Thandie THANDO <thandiee@...>
Date: Fri Aug 31, 2007 9:01 pm
Subject: Re: I am organizing a Rio trip for PMMA treatment
thandiee
Offline Offline
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Hi Philip

Thanks for the info. I have been contemplating on this
trip for a while one. I already sunk in $17,000 on my
butt augmentantion. Had implants and some fat transfer
done but I'm still not satisfied. Dr Gustein (beverly
Hills) did a great job but I still fill I need some of
the PMMA as a booster..hahaha.

i just started med school and my schedule is very
demanding and would love to get intouch with Dr serra
so I can schedule an appointment. How do you suppose I
can get hold of the man? Got his Tel# or email add? Is
he easy to communicate with? Please advise.

Thanks for taking your time and i'm sure some cash too
to coordinate these trips. I hope to be in your
company the next time around.

All the best
Thandiee


--- Philip <p461nyc@...> wrote:

> Hello everybody,
>
> This is just a reminder to anyone interested in
> going to Rio de
> Janeiro for PMMA treatment with Dr. Serra, that I am
> organizing
> another group trip for October 22nd - 26th.
>
> For those of you who don't know, I work as a
> volunteer to coordinate
> these trips for English and Spanish speaking
> patients who might
> otherwise find the idea of travel to Brazil, much
> less for medical
> treatment,to be a little (or very!) intimidating.
> Since I live in South America (ex-pat from NYC) this
> is relatively
> easy for me to do. I do these trips as an extension
> of the work of our
> non-profit foundation www.AestheticArgentina.org
>
> This will be the fourth trip this year as they are
> generally every
> three months or so.  In addition to giving me
> something to do :)
> ...its a great excuse for me to go to Rio for a week
> on a regular
> basis!  That is especially welcome right now as we
> are in the midst of
> a long winter here in Buenos Aires.
>
>  Aside from the obvious benefits of not going solo,
> there is a
> powerful effect spending a week with others who can
> relate to just
> about anything you are going through. The great
> majority of people who
> makeup these groups are extremely "positive" in
> every sense of the
> word; its my opinion that there is a strong
> connection between
> positive attitudes and long-term survivors.  The two
> seem to go
> together. So the group dynamic is especially
> powerful in this
> situation....not to mention a most beautiful
> setting.
>
> Normally we are between 6 and 10 patients in each
> group.
>
> If you are interested or know someone who is...here
> is how it works:
>
> The first step is to have a "virtual" consultation
> with Dr. Serra.
> This means that you send photos to me
> (confidentially of course)which
> I then forward to Dr. Serra. (By the way..I began
> doing this because
> although Dr. Serra is fluent in English, his office
> staff speaks only
> Portuguese, and he just does not have time to answer
> individual emails
> himself).
>
>  The most commonly treated areas are the Buttocks
> and Face. He also
> treats legs and arms that have lost their
> sub-cutaneous fat although
> with legs and arms the results are not nearly as
> dramatic as the
> Buttocks and Face which can be restored in many
> cases to more or less
> pre-lipoatrophy state.
>
>
> After he has reviewed the photos, I will send you
> the doctor's
> suggested treatment including the costs. Faces
> normally range between
> $750 and $1000 and can almost always be done in a
> single trip. The
> Buttocks restoration varies in cost depending on the
> size of the
> patient as well as the degree of tissue loss. On
> average the cost is
> between $2500 and $4000 (these prices were 20 to 30%
> less in the past
> but have increased lately due to the weakness of the
> dollar against
> the Real). Many patients can see enough improvement
> in the buttocks in
> one treatment;others elect to return (at least 90
> days later) for a
> second treatment.  A much smaller number will have a
> third, but this
> is usually just for finishing touches.
>
> Dr. Serra's clinic also has two other dermatologists
> who provide a
> full range of treatments.  This can be an added
> bonus in that the
> prices for cosmetic treatments are a fraction of
> what you would pay in
> the U.S. or Canada. So many patients choose to take
> advantage of the
> time in Rio to do a number of other procedures.
>
>
> I will help you plan your travel and assist with
> booking rooms,
> arranging the treatment appointments (I will go with
> you and accompany
> you back to the hotel),and just generally help out
> with any other
> details. The normal time needed in 5 days (arriving
> no later than
> Monday morning and departing no earlier than Friday
> afternoon.
> Round-trip airfare on average can be as low as $750
> or as high as
> $1200 depending on the season and airline special
> sales.
>
> The main purpose of this post is to answer the most
> frequently asked
> questions that I receive about the group travel. If
> you want other
> information about the treatment itself or Dr. Serra,
> please let me know.
>
> As I am often asked...I will also say that I don't
> receive payment or
> charge anything for the services I offer. However we
> are always happy
> to accept donations to the Foundation to help defray
> my personal
> travel and lodging expenses. That said, no one
> should ever feel any
> kind of obligation to offer anything.  I am very
> fortunate to have the
> time and ability to do this and helping out where I
> can is great
> compensation!
>
> As we are about 7 weeks from the trip, now is the
> time to begin
> planning and making arrangements. Dr. Serra needs
> advance notice to
> arrange his schedule for appointments, and you will
> need time to
> purchase airline tickets, and then process your
> travel visa for Brazil
> (which is good for 5 years and multiple entries).
>
> I am available to answer any questions you may have.
>
>
> All the best to everybody!
>
> Philip
> Buenos Aires
>
>




________________________________________________________________________________\
____
Pinpoint customers who are looking for what you sell.
http://searchmarketing.yahoo.com/

#22711 From: Nelson Vergel <nelsonvergel@...>
Date: Fri Aug 31, 2007 7:52 pm
Subject: Pozhealth will soon be 5 years old!
nelsonvergel
Offline Offline
Send Email Send Email
 
I created this group in September of 2002 and we know have 2500 members and
averaging around 300-350 emails a month

If you can not get your answers here, you cannot get them anywhere! :)

Thanks to all of you



Regards,
Nelson Vergel
powerusa dot org

#22710 From: Mark Meier <sactoswine@...>
Date: Fri Aug 31, 2007 6:13 pm
Subject: The Houston HIV Katrina and Single Payer System
sactoswine
Offline Offline
Send Email Send Email
 
So how does it work in a European-style single payer system? Is capitation used?  Is it like a giant, nationwide HMO, or are doctors paid by the visit?  We all know it's much, much cheaper, since payment rates to providers are negotiated by the state, and universally available by definition. But what are the ramifications with respect to getting appointments and finding the doctor you want?  And do you have to go through a primary care physician to get to a specialist?

#22709 From: "swagla" <SWagLA@...>
Date: Fri Aug 31, 2007 5:38 pm
Subject: Removing Bio-Alcamid Los Angeles
swagla
Offline Offline
Send Email Send Email
 
Hi,
Does anyone have a recommendation for a doctor in the Los Angeles area
who has experience removing Bio-Alcamid?
Thanks,
Sid

#22708 From: "Philip" <p461nyc@...>
Date: Fri Aug 31, 2007 6:14 pm
Subject: I am organizing a Rio trip for PMMA treatment
philipargentina
Offline Offline
Send Email Send Email
 
Hello everybody,

This is just a reminder to anyone interested in going to Rio de
Janeiro for PMMA treatment with Dr. Serra, that I am organizing
another group trip for October 22nd - 26th.

For those of you who don't know, I work as a volunteer to coordinate
these trips for English and Spanish speaking patients who might
otherwise find the idea of travel to Brazil, much less for medical
treatment,to be a little (or very!) intimidating.
Since I live in South America (ex-pat from NYC) this is relatively
easy for me to do. I do these trips as an extension of the work of our
non-profit foundation www.AestheticArgentina.org

This will be the fourth trip this year as they are generally every
three months or so.  In addition to giving me something to do :)
...its a great excuse for me to go to Rio for a week on a regular
basis!  That is especially welcome right now as we are in the midst of
a long winter here in Buenos Aires.

  Aside from the obvious benefits of not going solo, there is a
powerful effect spending a week with others who can relate to just
about anything you are going through. The great majority of people who
makeup these groups are extremely "positive" in every sense of the
word; its my opinion that there is a strong connection between
positive attitudes and long-term survivors.  The two seem to go
together. So the group dynamic is especially powerful in this
situation....not to mention a most beautiful setting.

Normally we are between 6 and 10 patients in each group.

If you are interested or know someone who is...here is how it works:

The first step is to have a "virtual" consultation with Dr. Serra.
This means that you send photos to me (confidentially of course)which
I then forward to Dr. Serra. (By the way..I began doing this because
although Dr. Serra is fluent in English, his office staff speaks only
Portuguese, and he just does not have time to answer individual emails
himself).

  The most commonly treated areas are the Buttocks and Face. He also
treats legs and arms that have lost their sub-cutaneous fat although
with legs and arms the results are not nearly as dramatic as the
Buttocks and Face which can be restored in many cases to more or less
pre-lipoatrophy state.


After he has reviewed the photos, I will send you the doctor's
suggested treatment including the costs. Faces normally range between
$750 and $1000 and can almost always be done in a single trip. The
Buttocks restoration varies in cost depending on the size of the
patient as well as the degree of tissue loss. On average the cost is
between $2500 and $4000 (these prices were 20 to 30% less in the past
but have increased lately due to the weakness of the dollar against
the Real). Many patients can see enough improvement in the buttocks in
one treatment;others elect to return (at least 90 days later) for a
second treatment.  A much smaller number will have a third, but this
is usually just for finishing touches.

Dr. Serra's clinic also has two other dermatologists who provide a
full range of treatments.  This can be an added bonus in that the
prices for cosmetic treatments are a fraction of what you would pay in
the U.S. or Canada. So many patients choose to take advantage of the
time in Rio to do a number of other procedures.


I will help you plan your travel and assist with booking rooms,
arranging the treatment appointments (I will go with you and accompany
you back to the hotel),and just generally help out with any other
details. The normal time needed in 5 days (arriving no later than
Monday morning and departing no earlier than Friday afternoon.
Round-trip airfare on average can be as low as $750 or as high as
$1200 depending on the season and airline special sales.

The main purpose of this post is to answer the most frequently asked
questions that I receive about the group travel. If you want other
information about the treatment itself or Dr. Serra, please let me know.

As I am often asked...I will also say that I don't receive payment or
charge anything for the services I offer. However we are always happy
to accept donations to the Foundation to help defray my personal
travel and lodging expenses. That said, no one should ever feel any
kind of obligation to offer anything.  I am very fortunate to have the
time and ability to do this and helping out where I can is great
compensation!

As we are about 7 weeks from the trip, now is the time to begin
planning and making arrangements. Dr. Serra needs advance notice to
arrange his schedule for appointments, and you will need time to
purchase airline tickets, and then process your travel visa for Brazil
(which is good for 5 years and multiple entries).

I am available to answer any questions you may have.

All the best to everybody!

Philip
Buenos Aires

#22707 From: PoWeRTX@...
Date: Fri Aug 31, 2007 12:38 pm
Subject: Therapeutic Human Papillomavirus Vaccine Safe and Immunogenic in Men Who Have Se
nelsonvergel
Offline Offline
Send Email Send Email
 

Therapeutic Human Papillomavirus Vaccine Safe and Immunogenic in Men Who Have Sex with Men

By Liz Highleyman

Two vaccines were recently approved for the prevention of human papillomavirus (HPV) infection, which can lead to cervical, anal, and other similar cancers. However, these vaccines are only effective in people who have not yet been infected, and do not prevent progression to cancer in people who already have "high-risk" (cancer-causing) HPV types.

Cervical cancer is an AIDS-defining illness, and anal cancer is a growing concern in HIV positive men, despite the use of HAART. To address this issue, Australian researchers are developing a therapeutic vaccine designed to prevent the development of anogenital cancer in people who are already infected with HPV

As reported at the recent 4th International AIDS Society Conference on HIV Pathogenesis, Treatment, and Prevention in Sydney, Australia (July 22-25), the investigators tested the candidate HPV-16 E6E7 vaccine in a study of 35 HIV-positive men who have sex with men in Melbourne and Sydney.

Most of the men (94%) were on HAART, and they had a current CD4 count of 627 cells/mm3 and a nadir (lowest-ever) CD4 count of 154 cells/mm3. The researchers tested the vaccine in people with HIV to see if it would stimulate an immune response in people with moderate immunosuppression.

All of the men were infected with high-risk HPV types, including HPV-16 (59%), HPV-18 (32%), and 9 other types (17%-41%); many had more than 1 type. Pap smears showed that most (80%) had some degree of abnormal anal cells at baseline, including low-grade anal intraepithelial neoplasia (AIN) (31%) and high-grade AIN (14%).

Participants were randomly assigned to receive either the HPV-16 E6E7 vaccine plus an adjuvant known as Iscomatrix at doses of 25 mg, 70 mg, or 240 mg, or else placebo injections. Three groups received injections on days 0, 28, and 84, while a fourth group received injections on days 0, 14, and 70.

Results

33 of the participants (94%) completed the study.

After 36 weeks of follow-up, the vaccine was generally well tolerated.

Most recipients reported moderate-to-severe short-term injection site reactions, as well as systemic reactions including headache, myalgia, and fatigue.

All participants maintained stable CD4 cell counts throughout the study.

5 participants had transient episodes of detectable viral load ("blips"), 3 of which returned below the limit of detection by the next test, and 2 of which occurred near the end of the study.

96% of vaccine recipients had at least a 4-fold increase in HPV-16 IgG antibodies from pre-vaccination levels.

71% had at least a 3-fold increase in interferon-gamma responses to the E6E7 peptides in the vaccine, but this did not appear to have a dose-response relationship.

There were no clear trends with regard to HPV detectability or anal disease progression.

2 vaccine recipients cleared HPV-16 (compared with zero in the placebo arm), but 3 others newly acquired HPV-16.

4 of 6 participants who started with high-grade AIN experienced resolution, but others developed new high-grade AIN during follow-up.

Conclusion

"The novel therapeutic HPV-16 E6E7 Iscomatrix vaccine appears safe and reasonably well tolerated" in HIV-positive people, the investigators concluded. "Antibody and cell-mediated immune responses were strong despite previous severe immunosuppression."

Given the promising results from this study, the researchers plan to conduct further clinical trials.

Carlton Clinic, Carlton, Australia; Alfred Hospital, Melbourne, Australia; STI Research Centre, University of Sydney, Australia; CSL Ltd, Melbourne, Australia; Prahran Market Clinic, South Yarra, Australia

08/31/07

Reference
J Anderson, J Hoy, R Hillman, and others. A randomised, placebo-controlled, dose escalation study to determine the safety, tolerability and immunogenicity of an HPV therapeutic vaccine in HIV-positive participants with oncogenic HPV infection of the anus. 4th International AIDS Society Conference on HIV Pathogenesis, Treatment, and Prevention. Sydney, Australia, July 22-25, 2007. Abstract MOPEB089.

 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





Get a sneak peek of the all-new AOL.com.

#22706 From: PoWeRTX@...
Date: Fri Aug 31, 2007 12:56 pm
Subject: Mayo Clinic trial finds flaxseed reduces hot flashes
nelsonvergel
Offline Offline
Send Email Send Email
 

Mayo Clinic trial finds flaxseed reduces hot flashes

The summer 2007 issue of the Journal of the Society for Integrative Oncology reported a study conducted at the Mayo Clinic which found that consuming flaxseed can help reduce uncomfortable hot flashes in postmenopausal women who are not using estrogen replacement therapy. Hot flashes are the primary reason women are prescribed estrogen by their physicians, however, recent research has linked synthetic hormone replacement with an increased risk of breast cancer and heart disease, resulting in an exodus of a large number of women from hormone treatment.

In a pilot study, breast health specialist Sandhya Pruthi, MD and colleagues gave 40 grams crushed flaxseed per day for six weeks to 29 women who suffered from hot flashes. The participants had not used any hormones, soy, or herbal supplements for the preceding four weeks. Questionnaires concerning the frequency and severity of hot flashes were administered before and after the treatment period. Twenty-one women completed the trial.

By the end of the study, hot flash frequency was cut in half and the overall “hot flash score” had diminished by an average of 57 percent. The women also reported improved mood, reduced joint or muscle pain, fewer chills, and less sweating.

Flaxseed was selected for the current trial because of its phytoestrogen content. Flax contains lignans that have mild estrogen-like effects as well as anticancer benefits. In recent trials, flax has been shown to help decrease the risk of breast cancer. The seeds are also a source of omega-3 fatty acids.

“We are quite pleased with the improvements noted by these women in their quality of life,” Dr Pruthi commented. “Not only does flaxseed seem to alleviate hot flashes, but it appears to have overall health and psychological benefits as well.”

“Hot flashes are a bothersome issue for women experiencing menopause,” she observed. “We hope to find more effective nonhormonal options to assist women, and flaxseed looks promising.”

 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





Get a sneak peek of the all-new AOL.com.

#22705 From: PoWeRTX@...
Date: Fri Aug 31, 2007 11:45 am
Subject: New Booklet for Salvage Patients by Dr Paul Bellman- NYC
nelsonvergel
Offline Offline
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New Booklet for Salvage Patients by Dr Paul Bellman- NYC

Paul Bellman is one of the most concerned doctors in the US on the subject of how to rescue HIV patients who have ran out of options. Here is a manuscript he wrote for patients and medical students on the subject that I highly recommend for all to read:

http://salvagetherapies.org/articals/salvageTreatment_ManualDrBellmanAug07
 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





Get a sneak peek of the all-new AOL.com.

#22704 From: PoWeRTX@...
Date: Fri Aug 31, 2007 11:20 am
Subject: What HIV meds penetrate the female genital track better?
nelsonvergel
Offline Offline
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I digested the conclusion a little for everyone.  Researchers need to stop using acronyms in their conclusions. So much work is done and it is transmitted so poorly.   Lay people should read conclusions and edit them for researchers!
 
In conclusion, this investigation is the first to comprehensively evaluate antiretroviral drug exposure in the female GT (genital track). Regardless of drug, genital track concentrations were detected 2-4 hours after a single antiretroviral dose. Additionally, GT exposures were similar after a first dose and at steady state. The results of this investigation support the use of 3TC (epivir), ZDV (AZT), TDF (viread), and potentially FTC (emtriva) as excellent PrEP/PEP (pre-exposure, post exposure) candidates. ATV (reyataz) and LPV/r (kaletra) may prove useful agents due to favorable GT concentrations in relation to HIV-1 wild-type susceptibility. We believe agents that achieve less than 10% of BP (blood plasma) exposure in the genital track, such as EFV (sustiva) and d4T (zerit) , are less likely PrEP/PEP candidates.”
*************************************
ART drug exposure in the female genital tract: implications for oral pre- and post-exposure prophylaxis

AIDS:Volume 21(14)September 2007p 1899-1907

Dumond, Julie Ba; Yeh, Rosa Fb; Patterson, Kristine Bc; Corbett, Amanda Ha; Jung, Byung Hwad; Rezk, Naser La; Bridges, Arlene Sa; Stewart, Paul Wa; Cohen, Myron Sc; Kashuba, Angela DMa
>From the aSchool of Pharmacy, University of North Carolina at Chapel Hill, North Carolina, USA
bCollege of Pharmacy, University of Houston, Texas, USA
cSchool of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
dBioanalysis and Biotransformation Research Center, Korea Institute of Science and Technology, Seoul, South Korea.

“…In conclusion, this investigation is the first to comprehensively evaluate antiretroviral drug exposure in the female GT. Regardless of drug, GT concentrations were detected 2-4 h after a single antiretroviral dose. Additionally, GT exposures were similar after a first dose and at steady state. The results of this investigation support the use of 3TC, ZDV, TDF, and potentially FTC as excellent PrEP/PEP candidates. ATV and LPV/r may prove useful agents due to favorable GT concentrations in relation to HIV-1 wild-type susceptibility. We believe agents that achieve less than 10% of BP exposure, such as EFV and d4T, are less likely PrEP/PEP candidates.”

Abstract
Objectives: To describe first dose and steady state antiretroviral drug exposure in the female genital tract.

Design: Non-blinded, single center, open-label pharmacokinetic study in HIV-infected women.

Method: Twenty-seven women initiating combination antiretroviral therapy underwent comprehensive blood plasma and cervicovaginal fluid sampling for drug concentrations during the first dose of antiretroviral therapy and at steady-state. Drug concentrations were measured by validated HPLC/UV or HPLC-MS/MS methods. Pharmacokinetic parameters were estimated for 11 drugs by non-compartmental analysis. Descriptive statistics and 95% confidence intervals were generated using Intercooled STATA Release 8.0 (Stata Corporation, College Station, Texas, USA).

Results:
For all antiretroviral drugs, genital tract concentrations were detected rapidly after the first dose. Drugs were stratified according to the genital tract concentrations achieved relative to blood plasma.

Median rank order of highest to lowest genital tract concentrations relative to blood plasma at steady state were:
lamivudine (concentrations achieved were 411% greater than blood plasma),
emtricitabine (395%),
zidovudine (235%)
tenofovir (75%),
ritonavir (26%),
didanosine (21%),
atazanavir (18%),
lopinavir (8%),
abacavir (8%),
stavudine (5%), and
efavirenz (0.4%).

Conclusions: This is the first study to comprehensively evaluate antiretroviral drug exposure in the female genital tract.
These findings support the use of lamivudine, zidovudine, tenofovir and emtricitabine as excellent pre-exposure/post-exposure prophylaxis (PrEP/PEP) candidates. Atazanavir and lopinavir might be useful agents for these applications due to favorable therapeutic indices, despite lower genital tract concentrations. Agents such as stavudine, abacavir, and efavirenz that achieve genital tract exposures less than 10% of blood plasma are less attractive PrEP/PEP candidates.

Introduction
Approximately 50% of adults living with HIV/AIDS are women [1]. Heterosexual HIV transmission is the most prominent mode of transmission in the developing world [2]. In Africa, where women account for an estimated 76% of HIV-infected persons aged 15-24 years [2], alternative methods to prevent sexual transmission are urgently needed. The oral administration of antiretroviral drugs to block HIV transmission is an attractive, minimally invasive approach to prevention [3]. This concept is already in practice domestically, as evidenced in the published United States guidelines for use in non-occupational post-exposure prophylaxis (nPEP) [4]. The increasing availability and use of generic antiretroviral drugs to treat HIV internationally would allow for the use of antiretroviral drugs for the prevention of HIV transmission in developing countries.

Early treatment with an effective antiretroviral drug regimen is most critical to preventing successful HIV transmission, as demonstrated by experience with nPEP and experimental animal models [5-10]. Employing antiretroviral drugs that concentrate quickly at the site of inoculation [i.e. genital tract (GT)] for pre-exposure prophylaxis (PrEP) and post-exposure prophylaxis (PEP) is a logical extension of this evidence. Therefore, we hypothesize that to prevent sexual transmission of HIV in women, oral antiretroviral drugs that achieve high concentrations quickly in the GT after a first dose would be optimal candidates for PEP or PrEP regimens. No human pharmacology data have, however, been generated in either healthy volunteers or HIV-infected cohorts that allow rational selection of drugs used for this purpose. To this end, we comprehensively evaluated antiretroviral drug exposure in the female GT of HIV-infected women for 11 commonly used antiretroviral medications in the three drug classes: nucleoside/tide analogue reverse transcriptase inhibitors (NRTI), non-nucleoside reverse transcriptase inhibitors (NNRTI), and protease inhibitors (PI).

Discussion
This is the first study to comprehensively evaluate antiretroviral drug exposure in the GT after single and multiple dosing. In this study of 27 HIV-infected women, GT concentrations of all 11 antiretroviral drugs reported here were detected rapidly after single doses. Differing GT exposures between the drugs relative to BP, however, suggest that only certain drugs may be preferable for PrEP or PEP regimens.

Of the nucleoside analogs evaluated, 3TC, ZDV, FTC, and TDF achieved GT concentrations similar to, or higher than, BP, and therefore would be excellent PEP and PrEP candidates for further study. Mean 3TC and ZDV concentrations in the GT were near or above extracellular concentrations suggested for clinical efficacy [20,21]. The median GT AUC of FTC at steady state was approximately three times higher than the suggested BP AUC of 10 ug*h/ml for clinical efficacy [23].

Of the other compounds studied, LPV and ATV achieved low to moderate GT concentrations. Since these may be similar to the recommended BP trough concentrations necessary for efficacy in patients with wild-type HIV-1 virus [22], further study of these agents is warranted for use in PrEP and PEP either given alone or in combination with NRTIs. EFV had very low GT concentrations relative to BP, and is unlikely to be useful in PEP/PrEP regimens.

Low drug exposures in the GT may contribute to higher viral shedding in the GT and the development of viral resistance. Recently, receipt of NNRTI-containing therapy was found to be independently associated with HIV shedding at the cervix (odds ratio = 2.24 compared to a PI-based regimen) in 107 women (31 on NVP and 76 on EFV) [24]. Additionally, data presented from the ACTG study A5077 suggested an increased rate of NNRTI mutations in the female GT [25] in individuals who were highly antiretroviral drug-experienced. Additionally, a recent study of 14 women found three with partial or complete compartmentalization of HIV in the GT compared to BP [26]. In our study, the low exposures of EFV (0.5% GT: BP AUC) observed in this study suggest NNRTI drug resistance to be biologically plausible [27,28]. As drug concentrations in the GT are seldom measured, however, a direct relationship between drug exposure, viral burden, and viral resistance patterns in the GT has not been established.

It is currently unclear which specific mechanisms and physicochemical properties of drugs dictate passage into the female GT. However, drug penetration appears to be related to the protein-binding capacity of each drug. Highly protein-bound drugs such as LPV (98-99% protein bound) [29] and ATV (86% protein bound) [30] had lower GT exposures (8 and 18%, respectively, at steady state), whereas drugs with low protein-binding such as the nucleoside/tide analogs ZDV, 3TC, and FTC (< 4% to < 38% protein bound) [31-33], generally had higher GT exposures (ranging from 235-411%). d4T and ddI were exceptions to this trend, as GT exposures were low (5 and 21%, respectively) despite < 5% protein binding [34,35]. For d4T, peak plasma concentrations occur at approximately 2 h post-dose. Since our first sampling time was 2 h post-dose, it is possible that the true peak concentration was not captured, and complete exposure information was not obtained.

To further this initial pharmacokinetic evaluation, a number of investigations are desirable. Linking drug exposure to biologic response (e.g., decrease in HIV RNA) in the female GT is critical to confirm that higher extracellular drug concentrations are predictive of a more potent response and guide drug selection for PrEP and PEP. Pharmacokinetic/pharmacodynamic modeling analyses are ongoing in our laboratory to evaluate the correlation between differential GT drug exposure and virologic response. Additionally, our previous NRTI work in male GT mononuclear cells suggests similar or lower concentrations of intracellular triphosphate active metabolites compared to BP despite higher GT extracellular drug exposures [36]. Therefore, research characterizing the intracellular active triphosphorylated metabolites for NRTIs in the female GT is necessary. Our study observed an extracellular half-life of TDF in the GT secretions twice as long as the extracellular half-life of TDF in BP, suggesting that TDF might be dosed at extended intervals for PEP or PrEP. Under first dose conditions, the median half-life was 14.5 h (95% CI: 3.6 - 29.2 h) in the GT, and 7.4 h (95% CI: 4.8-12.4 h) in BP (data not shown). However, characterizing intracellular concentrations of tenofovir diphosphate in GT mononuclear cells would be most important to move this application forward.

Although for most drugs, no differences in plasma drug exposure have been found between HIV-infected subjects and healthy volunteers [28-32], it may also be beneficial to evaluate the GT exposures of these drugs in healthy women, as they will be the primary recipients of PrEP and PEP. Additionally, no data exist on the influence of local infection and inflammation on drug concentrations in the female GT. As 130-1800% increases in drug concentrations have been documented with the inflammation present in meningitis and prostatitis, [37-39], GT infections may also increase antiretroviral drug concentrations in addition to increasing susceptibility to HIV infection [40-42].

Finally, understanding antiretroviral protein binding in the GT is necessary. This investigation measured total (protein unbound drug + protein bound drug) drug concentrations in both BP and GT. However, it has been suggested that concentrations of drug binding proteins (specifically albumin and alpha-1 acid glycoprotein) in the female GT may be lower than in BP [43]. If this is true, despite differences in total drug concentrations between BP and GT, free drug concentrations in the GT may be similar to, or greater than, BP. Hence, free drug concentrations may be a more important predictor of efficacy. Although these types of investigations are technically difficult and lend themselves better to in-vitro study, this work will be required for a more thorough understanding of antiretroviral behavior in the GT.

In conclusion, this investigation is the first to comprehensively evaluate antiretroviral drug exposure in the female GT. Regardless of drug, GT concentrations were detected 2-4 h after a single antiretroviral dose. Additionally, GT exposures were similar after a first dose and at steady state. The results of this investigation support the use of 3TC, ZDV, TDF, and potentially FTC as excellent PrEP/PEP candidates. ATV and LPV/r may prove useful agents due to favorable GT concentrations in relation to HIV-1 wild-type susceptibility. We believe agents that achieve less than 10% of BP exposure, such as EFV and d4T, are less likely PrEP/PEP candidates.


Results
Demographics
Demographic data for the 27 women enrolled are presented in Table 1. The study population was predominantly African American (70%), middle-aged (median: 35 years; IQR: 31-42 years), with a BP HIV RNA of 4.7 (IQR, 4.0-5.0) log10 copies/ml and a CD4+T-cell count of 307 (220-372) cells/μl at study entry. As most subjects were antiretroviral experienced (67%), the provider-selected regimens varied widely. Seventy percent (19/27) of the regimens contained 3TC. TDF was found in 56% of the regimens, ABC in 30%, and ZDV in 24%. Thirty-three percent of the women were on EFV-containing therapy, and 52% were on a PI-containing regimen (57% ATV/r, 36% LPV/r, and 7% ATV); one woman (4%) received EFV with LPV/r. Two individuals (7%) were on triple nucleoside therapy, and one (4%) received nevirapine. (Nevirapine data not presented.)

Antiretroviral pharmacokinetics in blood plasma and genital tract
Using the direct cervicovaginal aspirate sampling method, all drugs were detected in the GT 2-4 h after the first dose, and reached peak concentrations for the dosing interval by 4-6 h. Figure 1a-g depict individual pharmacokinetic profiles of selected antiretroviral drugs over their respective dosing intervals in BP and GT after a first dose and at steady state. These drugs were selected as achieving the highest concentrations in their respective drug classes, using doses and/or dosing regimens most commonly prescribed.

Nucleoside/tide reverse transcriptase inhibitors
Figure 1a depicts extracellular ZDV concentrations over a 12 h dosing interval. After a first dose, ZDV concentrations were detectable in both BP and GT secretions 2 h after a dose. Although BP concentrations steadily declined from that time point, GT concentrations continued to increase and reached a maximum concentration at 6 h post-dose. At steady state, concentrations were detectable in the GT, but not in BP, prior to dosing. The GT and BP concentrations were similar 4 h postdose; after this point, GT concentrations declined minimally, while BP concentrations declined significantly. An average extracellular BP concentration (Cav) previously suggested for efficacy [20,21], is indicated in the figure as a black horizontal line. GT concentrations were at or near this target for a longer period of time than BP concentrations.

Lamivudine exposure after once-daily dosing can be seen in Fig. 1b. Similar results were seen for subjects receiving twice daily dosing (not shown). GT concentrations were approximately 1-log higher than BP concentrations throughout the dosing interval after a single dose and under steady-state conditions. The GT concentrations exceeded the suggested average extracellular target concentration (Cav) previously suggested for efficacy [20,21]. Similarly, GT concentrations of FTC were higher than BP concentrations from 6-24 h after a single dose, and remained higher than BP concentrations during the entire dosing interval under steady-state conditions (Fig. 1c). For TDF (Fig. 1d), the GT concentrations were at or above BP concentrations 4 h after a dose, and remained higher throughout the dosing interval.

Protease inhibitors
Pharmacokinetic profiles for ATV and LPV are shown in Fig. 1e and f. In contrast to the NRTIs, ATV GT concentrations (when given as 300 mg ATV/100 mg RTV once daily) were lower than BP throughout the dosing interval both after first dose and at steady-state. These concentrations still, however, exceeded a suggested BP trough concentration of 150 ng/ml for efficacy against wild-type virus [22]: the mean (±SD) ATV trough concentration in the GT after a first dose was 417 ± 818 ng/ml, and at steady state was 169 ± 148 ng/ml. The GT concentrations for LPV were also lower than BP at both first dose and steady-state. A suggested LPV trough concentration for efficacy of 1000 ng/ml is depicted in Fig. 1f [22]. The GT concentrations approached this target over a dosing interval, and briefly exceed this concentration at the 4-h time point (mean ± SD = 1522 ± 1659 ng/ml). At the end of the dosing interval, mean ± SD GT concentrations were 437 ± 631 ng/ml after a single dose and 354 ± 384 ng/ml at steady-state.

Nonnucleoside reverse transcriptase inhibitors
The summary EFV pharmacokinetic profiles are shown in Fig. 1g. The BP and GT exposures are clearly distinct. Whereas EFV was detected in the GT 2 h after a single dose, concentrations were approximately 10 ng/ml: 2 logs lower than BP. The suggested target trough concentration for EFV is 1000 ng/ml [22].

Pharmacokinetic parameters
Table 2 lists steady-state pharmacokinetic parameter estimates in BP and GT for each drug. BP concentrations at the end of the dosing interval (C_) and the AUC over 24 h (AUC0-24h) for each drug were within the expected range. On average, GT time to maximal concentration (Tmax) was delayed in comparison with BP. All drugs were, however, detectable in GT secretions within 4 h of antiretroviral drug ingestion.

Fig. 1. (a) Mean (SE) pharmacokinetic profile of zidovudine (ZDV) over a 12 h dosing interval in blood plasma (BP) and genital tract (GT) at first dose and steady state. Subjects received 300 mg every 12 h. The solid line represents an extracellular target concentration previously suggested as efficacious in clinical studies [20,21]. (b) Mean (SE) pharmacokinetic profile of lamivudine (3TC) over a 24 h dosing interval in BP and GT at first dose and steady state. Subjects received 300 mg every 24 h. The solid line represents an extracellular target concentration previously suggested as efficacious in clinical studies [20,21]. (c) Mean (SE) pharmacokinetic profile of emtricitabine (FTC) over a 24 h dosing interval in BP and GT at first dose and steady state. Subjects received 200 mg every 24 h. No target concentration for clinical efficacy has been defined. (d) Mean (SE) pharmacokinetic profiles of tenofovir (TDF) over a 24 h dosing interval in BP and GT at first dose and steady state. Patients received 300 mg of TDF every 24 h. No target concentration for clinical efficacy has been defined. (e) Mean (SE) pharmacokinetic profile of atazanavir (ATV) over a 24 h dosing interval in BP and GT at first dose and steady state. Patient received 300 mg of ATV and 100 mg of ritonavir (RTV) every 24 h. The solid line represents the suggested clinical target concentration for ATV [22]. (f) Mean (SE) pharmacokinetic profile of lopinavir (LPV) over a 12 h dosing interval in BP and GT at first dose and steady state. Subjects received 400 mg of LPV and 100 mg of RTV every 12 h. The solid line represents a suggested clinical target concentration for LPV [22]. (g) Mean (SE) pharmacokinetic profile of efavirenz (EFV) over a 24 h dosing interval in BP and GT at first dose and steady state. Subjects received 600 mg of EFV every 24 h. The solid line represents a suggested clinical target concentration for EFV [22].








Table 3. Rank order by genital tract (GT): blood plasma (BP) area under the curve (AUC) ratio (%) at first dose.
ZDV, 3TC, and FTC achieved greater GT exposures than BP both after a single dose and under steady-state conditions. The median GT exposures for these drugs ranged from 111 to 371% that of BP after a single dose and 235 to 411% after multiple doses. TDF GT exposure at first dose achieved a median of 135%, and 75% of BP at steady state. In contrast, ATV, stavudine (d4T), EFV, and RTV achieved lower GT exposures than BP, ranging from 0.5 to 21% that of BP after a first dose, and 0.4 to 26% after multiple doses.



Methods
Study design and population
HIV-infected, non-pregnant adult women were enrolled in a non-blinded, observational, open-label prospective, pharmacokinetic study to assess first dose and steady-state antiretroviral drug exposure in cervicovaginal fluid (CVF) relative to blood plasma (BP) from November 2002 to May 2006. Subjects were recruited from the Infectious Diseases Clinic at the University of North Carolina at Chapel Hill. Exclusion criteria included the following: ≤ 17 years of age; active bacterial, fungal, or opportunistic GT or systemic infection at the time of enrollment; hysterectomy; pregnancy; hematocrit less than 30%; unable to abstain from sexual intercourse or douching for 48 h prior to study visits; unable to complete a dosing card; and an estimated drug adherence rate of < 80%, as determined by dosing card and patient self-report.

The antiretroviral drug regimen was selected by the patient's primary HIV provider. Women could be antiretroviral naive and initiating antiretroviral drugs, changing a failing regimen, or re-initiating antiretroviral drugs after a therapy interruption. All patients gave informed consent prior to study participation. This protocol was approved by the Biomedical Institutional Review Board of the University of North Carolina at Chapel Hill.

Before being enrolled into the study, patients underwent a routine pelvic examination, physical examination, extensive sexually transmitted infection (STI) screening, and routine safety laboratory tests, including a complete blood count, serum chemistries, liver function tests, and serum pregnancy testing. STI screening included testing for chlamydia and gonorrhea by cervical polymerase chain reaction (PCR), testing for trichomonas by urine culture and PCR [11], and testing for syphilis by serum rapid plasma reagin (RPR) with confirmatory treponemal testing if positive. STI testing was performed in the University of North Carolina Sexually Transmitted Diseases Cooperative Research Center Microbiology Core Lab or the McLendon Laboratories of the UNC Hospitals. Any patient with a STI at screening was referred to her primary provider for treatment, and then offered re-screening after successfully completing STI therapy.

Study visits
Following acceptable screening results, patients were admitted for an overnight stay in the Verne S. Caviness General Clinical Research Center. The first dose of the new antiretroviral drug regimen was observed, and six paired BP and CVF samples were obtained ('first dose' conditions). At least 3 weeks later, after continuing the regimen ('steady-state' conditions), patients returned to the research center whereby the first-dose BP and CVF sampling strategy was repeated after an observed dose. Patients were also followed monthly for an additional 6 months, with BP and GT samples obtained at a single time points 2 to 24 h postdose.

Sample collection and processing
Under both first dose and steady-state conditions, CVF and BP samples were obtained at 0 (immediately predose), 2, 4, 6, 12, and 24 h after observed doses of the antiretroviral drug regimen. All CVF samples were obtained via direct aspiration with a volumetric aspiration device. Subjects were instructed to remain supine for approximately 10 min prior to collection in order to pool CVF in the posterior fornix of the vagina for optimal collection volume. Samples at 0 and 24 h were obtained during a pelvic examination, and the remaining samples at 2, 4, 6, and 12 h post-dose were self-collected. CVF volumes typically ranged from 0.1 to 0.4 ml per sample. A previously conducted pilot study [12] demonstrated this method to be a reproducible and robust approach to specimen collection. To minimize any HIV RNA and drug concentration variability, all visits were scheduled in the 7 to 10 days following the end of menses.

After collection, directly aspirated CVF was transferred to labeled cryovials and stored at -80°C until analysis. Whole blood was obtained using K3EDTA-containing collection tubes (Becton Dickinson Diagnostics, Franklin Lakes, New Jersey, USA) and centrifuged at 1300 g (2600 rpm) at 4°C for 15 min. The resulting plasma was aliquoted into labeled cryovials and stored at -80°C until analysis. Drug concentrations in BP were measured using validated high performance liquid chromatography (HPLC)/UV methods [13-15], and concentrations in CVF were quantified using a validated HPLC-mass spectrometry (MS)/MS method [16].

Briefly, CVF concentrations were measured using a simultaneous assay for 17 antiretroviral drugs. After thawing, samples were centrifuged and the resultant supernatant underwent solid phase extraction using BOND ELUT C-18 columns (Varian, Harbor City, California, USA) as previously described [15]. Cimetidine (in acetate buffer, pH 5.0) was used as internal standard, and was applied directly to the conditioned column prior to CVF introduction. A Shimadzu solvent delivery system (Columbia, Maryland, USA) and a LEAP HTC Pal thermostatted (6°C) autosampler (Carrboro, North Carolina, USA) connected to an Applied Biosystems API4000 triple quandruple mass spectrometer and Turbospray ion source (Applied Biosystems, Foster City, California, USA) with an Aquasil C18 column (Thermo-Electron, San Jose, California, USA) was used for the analysis. Multiple reaction monitoring and positive-to-negative polarity switching were used. Assay sensitivity was 1 ng/ml for abacavir (ABC); 5 ng/ml for lamivudine (3TC), zidovudine (ZDV), emtricitabine (FTC), lopinavir (LPV), atazanavir(ATV) and efavirenz (EFV); and 10 ng/ml for tenofovir (TDF), didanosine (ddI), stavudine (d4T) and ritonavir (RTV). Overall assay precision was 2.0-14.3 CV%, and accuracy was 88-113%. Recovery for the drugs studied ranged from 80% for RTV and LPV to 99% for 3TC, ddI and ABC.

All analytical work was performed by the UNC Center for AIDS Research (CFAR) Clinical Pharmacology and Analytical Chemistry Core, which participates in quarterly national and international external proficiency testing [17,18]. These results consistently demonstrate high levels of accuracy and precision for our antiretroviral assays.

Data analysis methods
Pharmacokinetic parameters, including the area under the time-concentration curve (AUC0-τ), were estimated for both CVF and BP using WinNonlin (version 4.0.1, Pharsight, Inc. Mountain View, California, USA). For these computations, concentration measurements below the lower limit of detection were imputed as zero and those below the lower limit of quantitation (LLQ) were imputed as 1⁄2 LLQ. For each antiretroviral agent, the GT: BP AUC0-τ ratios were calculated, and multiplied by 100 to represent penetration of drug into the GT relative to BP [19]. Descriptive statistical methods, particularly medians and the interquartile range (IQR), were used in the primary analyses of these AUC ratios. The 95% confidence intervals of the median AUC ratios for each drug at each visit were calculated using Intercooled STATA Release 8.0 (Stata Corporation, College Station, Texas, USA).





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Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





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ART drug exposure in the female genital tract: implications for oral pre- and post-exposure prophylaxis

AIDS:Volume 21(14)September 2007p 1899-1907

Dumond, Julie Ba; Yeh, Rosa Fb; Patterson, Kristine Bc; Corbett, Amanda Ha; Jung, Byung Hwad; Rezk, Naser La; Bridges, Arlene Sa; Stewart, Paul Wa; Cohen, Myron Sc; Kashuba, Angela DMa
>From the aSchool of Pharmacy, University of North Carolina at Chapel Hill, North Carolina, USA
bCollege of Pharmacy, University of Houston, Texas, USA
cSchool of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
dBioanalysis and Biotransformation Research Center, Korea Institute of Science and Technology, Seoul, South Korea.

“…In conclusion, this investigation is the first to comprehensively evaluate antiretroviral drug exposure in the female GT. Regardless of drug, GT concentrations were detected 2-4 h after a single antiretroviral dose. Additionally, GT exposures were similar after a first dose and at steady state. The results of this investigation support the use of 3TC, ZDV, TDF, and potentially FTC as excellent PrEP/PEP candidates. ATV and LPV/r may prove useful agents due to favorable GT concentrations in relation to HIV-1 wild-type susceptibility. We believe agents that achieve less than 10% of BP exposure, such as EFV and d4T, are less likely PrEP/PEP candidates.”

Abstract
Objectives: To describe first dose and steady state antiretroviral drug exposure in the female genital tract.

Design: Non-blinded, single center, open-label pharmacokinetic study in HIV-infected women.

Method: Twenty-seven women initiating combination antiretroviral therapy underwent comprehensive blood plasma and cervicovaginal fluid sampling for drug concentrations during the first dose of antiretroviral therapy and at steady-state. Drug concentrations were measured by validated HPLC/UV or HPLC-MS/MS methods. Pharmacokinetic parameters were estimated for 11 drugs by non-compartmental analysis. Descriptive statistics and 95% confidence intervals were generated using Intercooled STATA Release 8.0 (Stata Corporation, College Station, Texas, USA).

Results:
For all antiretroviral drugs, genital tract concentrations were detected rapidly after the first dose. Drugs were stratified according to the genital tract concentrations achieved relative to blood plasma.

Median rank order of highest to lowest genital tract concentrations relative to blood plasma at steady state were:
lamivudine (concentrations achieved were 411% greater than blood plasma),
emtricitabine (395%),
zidovudine (235%)
tenofovir (75%),
ritonavir (26%),
didanosine (21%),
atazanavir (18%),
lopinavir (8%),
abacavir (8%),
stavudine (5%), and
efavirenz (0.4%).

Conclusions: This is the first study to comprehensively evaluate antiretroviral drug exposure in the female genital tract.
These findings support the use of lamivudine, zidovudine, tenofovir and emtricitabine as excellent pre-exposure/post-exposure prophylaxis (PrEP/PEP) candidates. Atazanavir and lopinavir might be useful agents for these applications due to favorable therapeutic indices, despite lower genital tract concentrations. Agents such as stavudine, abacavir, and efavirenz that achieve genital tract exposures less than 10% of blood plasma are less attractive PrEP/PEP candidates.

Introduction
Approximately 50% of adults living with HIV/AIDS are women [1]. Heterosexual HIV transmission is the most prominent mode of transmission in the developing world [2]. In Africa, where women account for an estimated 76% of HIV-infected persons aged 15-24 years [2], alternative methods to prevent sexual transmission are urgently needed. The oral administration of antiretroviral drugs to block HIV transmission is an attractive, minimally invasive approach to prevention [3]. This concept is already in practice domestically, as evidenced in the published United States guidelines for use in non-occupational post-exposure prophylaxis (nPEP) [4]. The increasing availability and use of generic antiretroviral drugs to treat HIV internationally would allow for the use of antiretroviral drugs for the prevention of HIV transmission in developing countries.

Early treatment with an effective antiretroviral drug regimen is most critical to preventing successful HIV transmission, as demonstrated by experience with nPEP and experimental animal models [5-10]. Employing antiretroviral drugs that concentrate quickly at the site of inoculation [i.e. genital tract (GT)] for pre-exposure prophylaxis (PrEP) and post-exposure prophylaxis (PEP) is a logical extension of this evidence. Therefore, we hypothesize that to prevent sexual transmission of HIV in women, oral antiretroviral drugs that achieve high concentrations quickly in the GT after a first dose would be optimal candidates for PEP or PrEP regimens. No human pharmacology data have, however, been generated in either healthy volunteers or HIV-infected cohorts that allow rational selection of drugs used for this purpose. To this end, we comprehensively evaluated antiretroviral drug exposure in the female GT of HIV-infected women for 11 commonly used antiretroviral medications in the three drug classes: nucleoside/tide analogue reverse transcriptase inhibitors (NRTI), non-nucleoside reverse transcriptase inhibitors (NNRTI), and protease inhibitors (PI).

Discussion
This is the first study to comprehensively evaluate antiretroviral drug exposure in the GT after single and multiple dosing. In this study of 27 HIV-infected women, GT concentrations of all 11 antiretroviral drugs reported here were detected rapidly after single doses. Differing GT exposures between the drugs relative to BP, however, suggest that only certain drugs may be preferable for PrEP or PEP regimens.

Of the nucleoside analogs evaluated, 3TC, ZDV, FTC, and TDF achieved GT concentrations similar to, or higher than, BP, and therefore would be excellent PEP and PrEP candidates for further study. Mean 3TC and ZDV concentrations in the GT were near or above extracellular concentrations suggested for clinical efficacy [20,21]. The median GT AUC of FTC at steady state was approximately three times higher than the suggested BP AUC of 10 ug*h/ml for clinical efficacy [23].

Of the other compounds studied, LPV and ATV achieved low to moderate GT concentrations. Since these may be similar to the recommended BP trough concentrations necessary for efficacy in patients with wild-type HIV-1 virus [22], further study of these agents is warranted for use in PrEP and PEP either given alone or in combination with NRTIs. EFV had very low GT concentrations relative to BP, and is unlikely to be useful in PEP/PrEP regimens.

Low drug exposures in the GT may contribute to higher viral shedding in the GT and the development of viral resistance. Recently, receipt of NNRTI-containing therapy was found to be independently associated with HIV shedding at the cervix (odds ratio = 2.24 compared to a PI-based regimen) in 107 women (31 on NVP and 76 on EFV) [24]. Additionally, data presented from the ACTG study A5077 suggested an increased rate of NNRTI mutations in the female GT [25] in individuals who were highly antiretroviral drug-experienced. Additionally, a recent study of 14 women found three with partial or complete compartmentalization of HIV in the GT compared to BP [26]. In our study, the low exposures of EFV (0.5% GT: BP AUC) observed in this study suggest NNRTI drug resistance to be biologically plausible [27,28]. As drug concentrations in the GT are seldom measured, however, a direct relationship between drug exposure, viral burden, and viral resistance patterns in the GT has not been established.

It is currently unclear which specific mechanisms and physicochemical properties of drugs dictate passage into the female GT. However, drug penetration appears to be related to the protein-binding capacity of each drug. Highly protein-bound drugs such as LPV (98-99% protein bound) [29] and ATV (86% protein bound) [30] had lower GT exposures (8 and 18%, respectively, at steady state), whereas drugs with low protein-binding such as the nucleoside/tide analogs ZDV, 3TC, and FTC (< 4% to < 38% protein bound) [31-33], generally had higher GT exposures (ranging from 235-411%). d4T and ddI were exceptions to this trend, as GT exposures were low (5 and 21%, respectively) despite < 5% protein binding [34,35]. For d4T, peak plasma concentrations occur at approximately 2 h post-dose. Since our first sampling time was 2 h post-dose, it is possible that the true peak concentration was not captured, and complete exposure information was not obtained.

To further this initial pharmacokinetic evaluation, a number of investigations are desirable. Linking drug exposure to biologic response (e.g., decrease in HIV RNA) in the female GT is critical to confirm that higher extracellular drug concentrations are predictive of a more potent response and guide drug selection for PrEP and PEP. Pharmacokinetic/pharmacodynamic modeling analyses are ongoing in our laboratory to evaluate the correlation between differential GT drug exposure and virologic response. Additionally, our previous NRTI work in male GT mononuclear cells suggests similar or lower concentrations of intracellular triphosphate active metabolites compared to BP despite higher GT extracellular drug exposures [36]. Therefore, research characterizing the intracellular active triphosphorylated metabolites for NRTIs in the female GT is necessary. Our study observed an extracellular half-life of TDF in the GT secretions twice as long as the extracellular half-life of TDF in BP, suggesting that TDF might be dosed at extended intervals for PEP or PrEP. Under first dose conditions, the median half-life was 14.5 h (95% CI: 3.6 - 29.2 h) in the GT, and 7.4 h (95% CI: 4.8-12.4 h) in BP (data not shown). However, characterizing intracellular concentrations of tenofovir diphosphate in GT mononuclear cells would be most important to move this application forward.

Although for most drugs, no differences in plasma drug exposure have been found between HIV-infected subjects and healthy volunteers [28-32], it may also be beneficial to evaluate the GT exposures of these drugs in healthy women, as they will be the primary recipients of PrEP and PEP. Additionally, no data exist on the influence of local infection and inflammation on drug concentrations in the female GT. As 130-1800% increases in drug concentrations have been documented with the inflammation present in meningitis and prostatitis, [37-39], GT infections may also increase antiretroviral drug concentrations in addition to increasing susceptibility to HIV infection [40-42].

Finally, understanding antiretroviral protein binding in the GT is necessary. This investigation measured total (protein unbound drug + protein bound drug) drug concentrations in both BP and GT. However, it has been suggested that concentrations of drug binding proteins (specifically albumin and alpha-1 acid glycoprotein) in the female GT may be lower than in BP [43]. If this is true, despite differences in total drug concentrations between BP and GT, free drug concentrations in the GT may be similar to, or greater than, BP. Hence, free drug concentrations may be a more important predictor of efficacy. Although these types of investigations are technically difficult and lend themselves better to in-vitro study, this work will be required for a more thorough understanding of antiretroviral behavior in the GT.

In conclusion, this investigation is the first to comprehensively evaluate antiretroviral drug exposure in the female GT. Regardless of drug, GT concentrations were detected 2-4 h after a single antiretroviral dose. Additionally, GT exposures were similar after a first dose and at steady state. The results of this investigation support the use of 3TC, ZDV, TDF, and potentially FTC as excellent PrEP/PEP candidates. ATV and LPV/r may prove useful agents due to favorable GT concentrations in relation to HIV-1 wild-type susceptibility. We believe agents that achieve less than 10% of BP exposure, such as EFV and d4T, are less likely PrEP/PEP candidates.


Results
Demographics
Demographic data for the 27 women enrolled are presented in Table 1. The study population was predominantly African American (70%), middle-aged (median: 35 years; IQR: 31-42 years), with a BP HIV RNA of 4.7 (IQR, 4.0-5.0) log10 copies/ml and a CD4+T-cell count of 307 (220-372) cells/μl at study entry. As most subjects were antiretroviral experienced (67%), the provider-selected regimens varied widely. Seventy percent (19/27) of the regimens contained 3TC. TDF was found in 56% of the regimens, ABC in 30%, and ZDV in 24%. Thirty-three percent of the women were on EFV-containing therapy, and 52% were on a PI-containing regimen (57% ATV/r, 36% LPV/r, and 7% ATV); one woman (4%) received EFV with LPV/r. Two individuals (7%) were on triple nucleoside therapy, and one (4%) received nevirapine. (Nevirapine data not presented.)

Antiretroviral pharmacokinetics in blood plasma and genital tract
Using the direct cervicovaginal aspirate sampling method, all drugs were detected in the GT 2-4 h after the first dose, and reached peak concentrations for the dosing interval by 4-6 h. Figure 1a-g depict individual pharmacokinetic profiles of selected antiretroviral drugs over their respective dosing intervals in BP and GT after a first dose and at steady state. These drugs were selected as achieving the highest concentrations in their respective drug classes, using doses and/or dosing regimens most commonly prescribed.

Nucleoside/tide reverse transcriptase inhibitors
Figure 1a depicts extracellular ZDV concentrations over a 12 h dosing interval. After a first dose, ZDV concentrations were detectable in both BP and GT secretions 2 h after a dose. Although BP concentrations steadily declined from that time point, GT concentrations continued to increase and reached a maximum concentration at 6 h post-dose. At steady state, concentrations were detectable in the GT, but not in BP, prior to dosing. The GT and BP concentrations were similar 4 h postdose; after this point, GT concentrations declined minimally, while BP concentrations declined significantly. An average extracellular BP concentration (Cav) previously suggested for efficacy [20,21], is indicated in the figure as a black horizontal line. GT concentrations were at or near this target for a longer period of time than BP concentrations.

Lamivudine exposure after once-daily dosing can be seen in Fig. 1b. Similar results were seen for subjects receiving twice daily dosing (not shown). GT concentrations were approximately 1-log higher than BP concentrations throughout the dosing interval after a single dose and under steady-state conditions. The GT concentrations exceeded the suggested average extracellular target concentration (Cav) previously suggested for efficacy [20,21]. Similarly, GT concentrations of FTC were higher than BP concentrations from 6-24 h after a single dose, and remained higher than BP concentrations during the entire dosing interval under steady-state conditions (Fig. 1c). For TDF (Fig. 1d), the GT concentrations were at or above BP concentrations 4 h after a dose, and remained higher throughout the dosing interval.

Protease inhibitors
Pharmacokinetic profiles for ATV and LPV are shown in Fig. 1e and f. In contrast to the NRTIs, ATV GT concentrations (when given as 300 mg ATV/100 mg RTV once daily) were lower than BP throughout the dosing interval both after first dose and at steady-state. These concentrations still, however, exceeded a suggested BP trough concentration of 150 ng/ml for efficacy against wild-type virus [22]: the mean (±SD) ATV trough concentration in the GT after a first dose was 417 ± 818 ng/ml, and at steady state was 169 ± 148 ng/ml. The GT concentrations for LPV were also lower than BP at both first dose and steady-state. A suggested LPV trough concentration for efficacy of 1000 ng/ml is depicted in Fig. 1f [22]. The GT concentrations approached this target over a dosing interval, and briefly exceed this concentration at the 4-h time point (mean ± SD = 1522 ± 1659 ng/ml). At the end of the dosing interval, mean ± SD GT concentrations were 437 ± 631 ng/ml after a single dose and 354 ± 384 ng/ml at steady-state.

Nonnucleoside reverse transcriptase inhibitors
The summary EFV pharmacokinetic profiles are shown in Fig. 1g. The BP and GT exposures are clearly distinct. Whereas EFV was detected in the GT 2 h after a single dose, concentrations were approximately 10 ng/ml: 2 logs lower than BP. The suggested target trough concentration for EFV is 1000 ng/ml [22].

Pharmacokinetic parameters
Table 2 lists steady-state pharmacokinetic parameter estimates in BP and GT for each drug. BP concentrations at the end of the dosing interval (C_) and the AUC over 24 h (AUC0-24h) for each drug were within the expected range. On average, GT time to maximal concentration (Tmax) was delayed in comparison with BP. All drugs were, however, detectable in GT secretions within 4 h of antiretroviral drug ingestion.

Fig. 1. (a) Mean (SE) pharmacokinetic profile of zidovudine (ZDV) over a 12 h dosing interval in blood plasma (BP) and genital tract (GT) at first dose and steady state. Subjects received 300 mg every 12 h. The solid line represents an extracellular target concentration previously suggested as efficacious in clinical studies [20,21]. (b) Mean (SE) pharmacokinetic profile of lamivudine (3TC) over a 24 h dosing interval in BP and GT at first dose and steady state. Subjects received 300 mg every 24 h. The solid line represents an extracellular target concentration previously suggested as efficacious in clinical studies [20,21]. (c) Mean (SE) pharmacokinetic profile of emtricitabine (FTC) over a 24 h dosing interval in BP and GT at first dose and steady state. Subjects received 200 mg every 24 h. No target concentration for clinical efficacy has been defined. (d) Mean (SE) pharmacokinetic profiles of tenofovir (TDF) over a 24 h dosing interval in BP and GT at first dose and steady state. Patients received 300 mg of TDF every 24 h. No target concentration for clinical efficacy has been defined. (e) Mean (SE) pharmacokinetic profile of atazanavir (ATV) over a 24 h dosing interval in BP and GT at first dose and steady state. Patient received 300 mg of ATV and 100 mg of ritonavir (RTV) every 24 h. The solid line represents the suggested clinical target concentration for ATV [22]. (f) Mean (SE) pharmacokinetic profile of lopinavir (LPV) over a 12 h dosing interval in BP and GT at first dose and steady state. Subjects received 400 mg of LPV and 100 mg of RTV every 12 h. The solid line represents a suggested clinical target concentration for LPV [22]. (g) Mean (SE) pharmacokinetic profile of efavirenz (EFV) over a 24 h dosing interval in BP and GT at first dose and steady state. Subjects received 600 mg of EFV every 24 h. The solid line represents a suggested clinical target concentration for EFV [22].








Table 3. Rank order by genital tract (GT): blood plasma (BP) area under the curve (AUC) ratio (%) at first dose.
ZDV, 3TC, and FTC achieved greater GT exposures than BP both after a single dose and under steady-state conditions. The median GT exposures for these drugs ranged from 111 to 371% that of BP after a single dose and 235 to 411% after multiple doses. TDF GT exposure at first dose achieved a median of 135%, and 75% of BP at steady state. In contrast, ATV, stavudine (d4T), EFV, and RTV achieved lower GT exposures than BP, ranging from 0.5 to 21% that of BP after a first dose, and 0.4 to 26% after multiple doses.



Methods
Study design and population
HIV-infected, non-pregnant adult women were enrolled in a non-blinded, observational, open-label prospective, pharmacokinetic study to assess first dose and steady-state antiretroviral drug exposure in cervicovaginal fluid (CVF) relative to blood plasma (BP) from November 2002 to May 2006. Subjects were recruited from the Infectious Diseases Clinic at the University of North Carolina at Chapel Hill. Exclusion criteria included the following: ≤ 17 years of age; active bacterial, fungal, or opportunistic GT or systemic infection at the time of enrollment; hysterectomy; pregnancy; hematocrit less than 30%; unable to abstain from sexual intercourse or douching for 48 h prior to study visits; unable to complete a dosing card; and an estimated drug adherence rate of < 80%, as determined by dosing card and patient self-report.

The antiretroviral drug regimen was selected by the patient's primary HIV provider. Women could be antiretroviral naive and initiating antiretroviral drugs, changing a failing regimen, or re-initiating antiretroviral drugs after a therapy interruption. All patients gave informed consent prior to study participation. This protocol was approved by the Biomedical Institutional Review Board of the University of North Carolina at Chapel Hill.

Before being enrolled into the study, patients underwent a routine pelvic examination, physical examination, extensive sexually transmitted infection (STI) screening, and routine safety laboratory tests, including a complete blood count, serum chemistries, liver function tests, and serum pregnancy testing. STI screening included testing for chlamydia and gonorrhea by cervical polymerase chain reaction (PCR), testing for trichomonas by urine culture and PCR [11], and testing for syphilis by serum rapid plasma reagin (RPR) with confirmatory treponemal testing if positive. STI testing was performed in the University of North Carolina Sexually Transmitted Diseases Cooperative Research Center Microbiology Core Lab or the McLendon Laboratories of the UNC Hospitals. Any patient with a STI at screening was referred to her primary provider for treatment, and then offered re-screening after successfully completing STI therapy.

Study visits
Following acceptable screening results, patients were admitted for an overnight stay in the Verne S. Caviness General Clinical Research Center. The first dose of the new antiretroviral drug regimen was observed, and six paired BP and CVF samples were obtained ('first dose' conditions). At least 3 weeks later, after continuing the regimen ('steady-state' conditions), patients returned to the research center whereby the first-dose BP and CVF sampling strategy was repeated after an observed dose. Patients were also followed monthly for an additional 6 months, with BP and GT samples obtained at a single time points 2 to 24 h postdose.

Sample collection and processing
Under both first dose and steady-state conditions, CVF and BP samples were obtained at 0 (immediately predose), 2, 4, 6, 12, and 24 h after observed doses of the antiretroviral drug regimen. All CVF samples were obtained via direct aspiration with a volumetric aspiration device. Subjects were instructed to remain supine for approximately 10 min prior to collection in order to pool CVF in the posterior fornix of the vagina for optimal collection volume. Samples at 0 and 24 h were obtained during a pelvic examination, and the remaining samples at 2, 4, 6, and 12 h post-dose were self-collected. CVF volumes typically ranged from 0.1 to 0.4 ml per sample. A previously conducted pilot study [12] demonstrated this method to be a reproducible and robust approach to specimen collection. To minimize any HIV RNA and drug concentration variability, all visits were scheduled in the 7 to 10 days following the end of menses.

After collection, directly aspirated CVF was transferred to labeled cryovials and stored at -80°C until analysis. Whole blood was obtained using K3EDTA-containing collection tubes (Becton Dickinson Diagnostics, Franklin Lakes, New Jersey, USA) and centrifuged at 1300 g (2600 rpm) at 4°C for 15 min. The resulting plasma was aliquoted into labeled cryovials and stored at -80°C until analysis. Drug concentrations in BP were measured using validated high performance liquid chromatography (HPLC)/UV methods [13-15], and concentrations in CVF were quantified using a validated HPLC-mass spectrometry (MS)/MS method [16].

Briefly, CVF concentrations were measured using a simultaneous assay for 17 antiretroviral drugs. After thawing, samples were centrifuged and the resultant supernatant underwent solid phase extraction using BOND ELUT C-18 columns (Varian, Harbor City, California, USA) as previously described [15]. Cimetidine (in acetate buffer, pH 5.0) was used as internal standard, and was applied directly to the conditioned column prior to CVF introduction. A Shimadzu solvent delivery system (Columbia, Maryland, USA) and a LEAP HTC Pal thermostatted (6°C) autosampler (Carrboro, North Carolina, USA) connected to an Applied Biosystems API4000 triple quandruple mass spectrometer and Turbospray ion source (Applied Biosystems, Foster City, California, USA) with an Aquasil C18 column (Thermo-Electron, San Jose, California, USA) was used for the analysis. Multiple reaction monitoring and positive-to-negative polarity switching were used. Assay sensitivity was 1 ng/ml for abacavir (ABC); 5 ng/ml for lamivudine (3TC), zidovudine (ZDV), emtricitabine (FTC), lopinavir (LPV), atazanavir(ATV) and efavirenz (EFV); and 10 ng/ml for tenofovir (TDF), didanosine (ddI), stavudine (d4T) and ritonavir (RTV). Overall assay precision was 2.0-14.3 CV%, and accuracy was 88-113%. Recovery for the drugs studied ranged from 80% for RTV and LPV to 99% for 3TC, ddI and ABC.

All analytical work was performed by the UNC Center for AIDS Research (CFAR) Clinical Pharmacology and Analytical Chemistry Core, which participates in quarterly national and international external proficiency testing [17,18]. These results consistently demonstrate high levels of accuracy and precision for our antiretroviral assays.

Data analysis methods
Pharmacokinetic parameters, including the area under the time-concentration curve (AUC0-τ), were estimated for both CVF and BP using WinNonlin (version 4.0.1, Pharsight, Inc. Mountain View, California, USA). For these computations, concentration measurements below the lower limit of detection were imputed as zero and those below the lower limit of quantitation (LLQ) were imputed as 1⁄2 LLQ. For each antiretroviral agent, the GT: BP AUC0-τ ratios were calculated, and multiplied by 100 to represent penetration of drug into the GT relative to BP [19]. Descriptive statistical methods, particularly medians and the interquartile range (IQR), were used in the primary analyses of these AUC ratios. The 95% confidence intervals of the median AUC ratios for each drug at each visit were calculated using Intercooled STATA Release 8.0 (Stata Corporation, College Station, Texas, USA).





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#22703 From: John Barrow <pozbod@...>
Date: Fri Aug 31, 2007 2:46 pm
Subject: Re:Jaundice
johnftl59
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A hint of jaundice is a frequent issue when starting Reyataz, and it
should resolve soon.

JB

#22702 From: PoWeRTX@...
Date: Fri Aug 31, 2007 11:36 am
Subject: Are we losing our mental capacity?
nelsonvergel
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This study really worries me. Median CD4 cells were in the 400, and half were naive. So these are not sick patients.  I wish they had defined what mild cognitive impairment is.  I forget faces, names, things to do, sometimes important personal data, etc.   At 48 years old, I have the feeling that this is not normal.  Studies like this one just feed that concern....
They say that may be most of the HIV meds we are taking may not be penetrating the central nervous system as well as they should, and thus we may be losing mental capacity with time.
I wonder if anyone is doing studies with the use of Alzheimer drugs for HIV related cognitive impairment....

Link:
The prevalence and incidence of neurocognitive impairment in the HAART era (08/30/07)
 
 
The study conclusions:
 
"....By the most conservative estimate, an assessment of neurocognitive function revealed that 26% of subjects selected from the ALLRT study were cognitively impaired at their baseline Neuroscreen....226 (58%) had a follow-up visit at which their test scores indicated they were neurologically unimpaired. This may be related to the favorable effects of HAART on neurological function
There was a relationship between immunological status and prevalent neurocognitive impairment, but we did not find substantial evidence to suggest that virological factors were associated with prevalent neurocognitive impairment....
 
the observed decline in neurocognitive functioning despite ART is consistent with the hypothesis that viral replication in the CNS may not be well controlled in some patients treated with HAART, perhaps because antiretroviral drugs may not penetrate adequately into the CNS..."
 
 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





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#22701 From: PoWeRTX@...
Date: Fri Aug 31, 2007 10:58 am
Subject: FDA Safety Changes: Truvada
nelsonvergel
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Emtricitabine/Tenofovir Disoproxil Fumarate (Truvada) Linked to Risk for Renal Impairment, HBV Exacerbation

On May 21, the FDA approved the safety labeling revisions for emtricitabine and tenofovir disoproxil fumarate 200-mg/300-mg tablets (Truvada, made by Gilead Sciences, Inc) to warn of the risk for renal impairment and the risk for exacerbation of hepatitis B virus infection (HBV) in patients coinfected with HIV and HBV.

Emtricitabine and tenofovir are principally eliminated by the kidney, and cases of renal impairment, including those of acute renal failure and Fanconi syndrome (renal tubular injury with severe hypophosphatemia), have been associated with its use.

Therefore, the FDA advises that creatinine clearance (CrCl) be calculated before initiation of therapy. No dose adjustments are required for patients with mild renal impairment (CrCl, 50 - 80 mL/minute); for patients with CrCl ranging from 30 to 49 mL/minute, the dosing interval should be extended from 24 to 48 hours.

Emtricitabine and tenofovir tablets should not be used in patients with a CrCl of less than 30 mL/minute or those requiring hemodialysis. Concomitant or recent use of other nephrotoxic agents should be avoided, and routine monitoring of CrCl and serum phosphorus is recommended in patients at risk for renal impairment.

The FDA notes that these recommendations are based on modeling of single-dose pharmacokinetic data in non–HIV-infected subjects and have not been clinically evaluated. Therefore, clinical response and renal function should be monitored closely during treatment.

Combination tablets containing emtricitabine and tenofovir are indicated for use with other antiretroviral agents in the treatment of HIV-1 infection. They have not been approved for the treatment of chronic HBV, and severe acute exacerbations of HBV have been reported in patients with coinfection who have discontinued either component. Close hepatic monitoring is advised for patients with HIV and HBV, with both clinical and laboratory follow-up for at least several months' duration on discontinuation of treatment; initiation of anti-HBV therapy may be warranted.

 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





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#22700 From: PoWeRTX@...
Date: Fri Aug 31, 2007 11:24 am
Subject: Sperm Washing-safety/efficacy Serodiscordant couples
nelsonvergel
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Now that California will be allowing sperm washing...I wonder how much it will cost . I know some countries in Europe have allowed it for years. As many of us live longer and are not as afraid of early death, some people want to reconsider having children....
 
NATAP http://natap.org/
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Safety and efficacy of sperm washing in HIV-1-serodiscordant couples where the male is infected: results from the European CREAThE network

AIDS:Volume 21(14)September 2007p 1909-1914

Bujan, Louisa; Hollander, Litalb; Coudert, Mathieua; Gilling-Smith, Carolec; Vucetich, Alexandrab; Guibert, Julietted; Vernazza, Pietroe; Ohl, Jeaninef; Weigel, Michaelg; Englert, Yvonh; Semprini, Augusto Eb; for the CREAThE network
From the aUniversity Toulouse III Paul Sabatier, EA 3694, Research Group on Human Fertility and CECOS Midi-Pyrénées, Toulouse, France
bESMAN Medical Consulting, Milan, Italy
cDepartment of Obstetrics and Gynaecology, Chelsea & Westminster Hospital, London, UK
dAPHP, Hôpital Cochin - Université Paris Descartes, Unité de Médecine de la Reproduction Service de Gynécologie-obstétrique, Paris, France
eInfectious Diseases, Department of Medicine. Kantonsspital, St Gallen, Switzerland
fCentre d'AMP de Strasbourg, Service de Gynécologie-Obstétrique, CMCO-SIHCUS, Schiltigheim, France
gDepartment Obstetric and Gynaecology, University Hospital of Mannheim, Leopoldina-Krankenhaus, Schweinfurt, Germany
hFertility Clinic, Department of Obstetrics and Gynaecology, Erasme Hospital and Laboratory for Research in Human Reproduction, Medicine Faculty, Free University Brussels, Belgium.
*for REproductive Assistance Techniques for HIV in Europe.

“….A total of 580 pregnancies were obtained from 3315 cycles. Pregnancy outcome was unknown in 47 cases. The 533 pregnancies resulted in 410 deliveries and 463 live births. The result of female HIV testing after assisted reproduction was known in 967 out of 1036 woman (7.1% lost to follow-up). All tests recorded were negative. The calculated probability of contamination was equal to zero….

“….The present study is the first multicentre study of the use of sperm washing in HIV-1-serodiscordant couples, in which the male partner was infected, who wished to conceive. It is the largest series published to date and the first with sufficient case numbers to confirm the safety and efficacy of assisted reproduction, where sperm washing was used as the primary means of avoiding HIV infection in the female partner. We recommend that public health authorities sustain and promote networks in order to analyse the results of assisted reproduction programmes, tailored to the needs of HIV-serodiscordant couples, and ensure a comprehensive database for the outcome of treatment and follow-up of all female patients treated is maintained, thereby facilitating epidemiologic studies…..

…..According to our present data and other studies that have demonstrated the feasibility of such approach (see review by Gilling-Smith et al. [31]) it is neither ethically nor legally justifiable to exclude individuals from infertility services on the basis of male HIV-infection. For many countries in the world the first priority of the policy against HIV is to improve education, to allow access to HIV screening, to encourage condom use and to offer antiretroviral therapy where appropriate. In countries where these approaches are now in place we recommended that assisted reproductive programmes, such as IUI with sperm washing, should be integrated into a global public health initiative against HIV….”

Abstract
Objective: To examine the safety and effectiveness of assisted reproduction using sperm washing for HIV-1-serodiscordant couples wishing to procreate where the male partner is infected.

Design and methods: A retrospective multicentre study at eight centres adhering on the European network CREAThE and involving 1036 serodiscordant couples wishing to procreate. Sperm washing was used to obtain motile spermatozoa for
3390 assisted reproduction cycles (2840 intrauterine inseminations, 107 in-vitro fertilizations, 394 intra-cytoplasmic sperm injections and 49 frozen embryo transfers). An HIV test was performed in female partners at least 6 months after assisted reproduction attempt. The outcome measures recorded were number of assisted reproduction cycles, pregnancy outcome and HIV test on women post-treatment.

Results: A total of 580 pregnancies were obtained from 3315 cycles. Pregnancy outcome was unknown in 47 cases. The 533 pregnancies resulted in 410 deliveries and 463 live births. The result of female HIV testing after assisted reproduction was known in 967 out of 1036 woman (7.1% lost to follow-up).
All tests recorded were negative. The calculated probability of contamination was equal to zero (95% confidence interval, 0-0.09%).

Conclusion:
This first multicentre retrospective study of assisted reproduction following sperm washing demonstrates the method to be effective and to significantly reduce HIV-1 transmission risk to the uninfected female partner. These results support the view that assisted reproduction with sperm washing could not be denied to serodiscordant couples in developed countries and, where possible, could perhaps be integrated into a global public health initiative against HIV in developing countries.

Introduction
According to the latest UNAIDS/World Health Organization (WHO) update (December 2006), the total number of people living with HIV had reached 39.5 million. As the AIDS epidemic continues to take a massive and global toll on human lives, the call for comprehensive strategies to prevent HIV transmission has never been higher. A fundamental policy in halting the spread of HIV has been the encouragement and facilitation of condom use in vaginal and anal sexual contacts. This approach however raises a major dilemma for serodiscordant couples, where the male partner is infected, who wish to conceive. These couples form an increasing part of the HIV population in developed countries, where most individuals infected with HIV are of reproductive age and able to access effective antiretroviral treatment. Improved life expectancy and quality has enabled these individuals to reanalyse their future and consider parenting as a socially and ethically acceptable option and many now express the desire for parenthood [1-3] as a fundamental part of healthy family life and return to normality. Recently published guidelines from the American Society for Reproductive Medicine (ASRM) and ethics recommendations concerning assisted reproduction on people infected by virus have been modified to allow assisted reproduction in HIV-serodiscordant couples [4].

The desire to conceive could counteract preventive barrier methods such as condom use if couples do not receive sufficient information on reproductive options to reduce viral transmission risk. Adoption and assisted reproduction from donor sperm are two reproductive options available to couples which totally eliminate the risk of HIV transmission. However, both methods are not equally available throughout Europe and both deny the infected person a genetic link to his child and could reinforce feelings of stigma and discrimination. Unprotected intercourse restricted to the time of ovulation may limit the risk of HIV transmission but from the limited data available, transmission has been shown to occur under these conditions [5]. One way of allowing HIV-serodiscordant couples, where the male is infected, to conceive their biological children while limiting the risk of HIV transmission is the use of assisted reproduction after semen processing using the sperm washing method. Sperm washing, as a means of preventing female infection in HIV-1-serodiscordant couples where the male partner is infected, was first proposed 17 years ago at a time when no methods were available to detect HIV-1 nucleic acids in sperm and before the introduction of highly active antiretroviral treatment (HAART) [6]. Since then, several publications have reported the results of different sperm washing programmes in such couples [7-18].

The mean risk of sexual HIV-1 transmission for a single act of penile-vaginal intercourse appears to be on the order of 0.1% (see review by Bartin and Overbaugh [19]). Therefore, it is not easy to establish whether sperm washing and assisted reproduction actually reduces the risk of transmission in a significant way.

In Europe, centres involved in sperm washing programmes have created the CREAThE network (Centre for REproductive Assisted Techniques for HIV in Europe) whose primary objective is to pool knowledge, experience and results in order to improve the service offered to HIV-serodiscordant couples.

The present retrospective study analysed pooled data, from eight centres involved in the CREAThE network, to study the safety and efficacy of assisted reproduction with sperm washing in the largest series of sperm washing cases ever performed in serodiscordant couples where the male partner was HIV-1 positive.

Materials and methods
Eight centres from six European countries participated in retrospective data collection on assisted reproduction cycles performed between 1989 to 2003 (Table 1). Serodiscordant couples (n = 1036) in which the male partner was infected with HIV-1, attended the centres to follow a sperm washing programme. Variables concerning HIV-1 infection in the man, age of the woman at the time of treatment, and past gynaecological history were recorded from the patients' data in each centre. A fertility screen was performed for both partners. Sperm washing was performed according to published methods [6,9] with minor adaptations in each centre. Briefly, sperm washing has been previously reported using three steps: step 1, a spermatozoa migration on density gradient; step2, repeated washing of the migrated pellet, step 3, a spermatozoa swim up. Sperm washing was performed on one or more semen samples according to the protocol used in each centre. Briefly the sperm obtained after a recommended 3-7 days of abstinence was submitted to a separation following density gradient centrifugation. The 90% fraction was centrifuged and washed (method with two steps only) or submitted to a swim up method (method with three steps). The London, Strasbourg, Mannheim and Toulouse centres systematically performed the preparation with three steps and the Brussels and Milan centres also performed three steps except when there was a fertility issue where only the two-step method was performed. The St Gallen and Paris centres used only the two-step method and St Gallen used a specific double tube technique that has been reported [20]. The aim of all these sperm washing methods was to select only motile spermatozoa free of seminal plasma and semen cells such as leukocytes.

After its introduction into clinical use (1995-1997), HIV-1 genome detection was performed according to published methods [21] on the final fraction of spermatozoa obtained after sperm washing, except in the St Gallen centre where a more stringent separation method was used [20]. If HIV-1 RNA or DNA were not detected in the isolated spermatozoa fraction, fresh spermatozoa (Brussels, Milan, London) or frozen-thawed spermatozoa (Brussels, Milan, London, Paris, Strasbourg, Mannheim, Toulouse) fractions were used. Washed samples with detectable HIV-genomes were not used for assisted reproduction.

The assisted reproduction procedure choice (intra-uterine insemination (IUI), in-vitro fertilization (IVF) or intra-cytoplasmic sperm injection (ICSI)) was based on the result of the couple's fertility screen and each centre's protocols. Supernumerary embryos obtained after IVF or ICSI were frozen with the possibility of being transferred in a subsequent cycle (frozen embryo transfer; FET) if pregnancy did not occur after the first embryo transfer. Following each assisted reproduction cycle with washed sperm, HIV screening was performed on the female partners. The result of a HIV-test performed at least 6 months after the last assisted reproduction treatment was recorded in the database for this study.

Table 1. Patients and assisted reproduction cycles performed according to the centres involved on CREAThE network.

IUI, intra-uterine insemination; IVF, in-vitro fertilization; ICSI, intra cytoplasmic sperm injection; FET, frozen embryo transfer.
MPatients for whom the result of HIV test was unknown at least 6 months after the last assisted reproduction attempt.


All couples were required to systematically use condoms during intercourse throughout the period of treatment. They were informed about the assisted reproduction procedure and the fact that sperm washing may not totally eliminate transmission risk. All couples gave their informed consent to the assisted reproduction with sperm washing and the procedure was done in accordance with the declaration of Helsinki. In accordance with each country's laws, an agreement by an institutional review board was obtained. A limited number of anonymized clinical data for each patient from each centre were recorded in a central database and statistical analysis was performed using STATA software version 8.0 (StataCorp LP, College Station, Texas, USA). The probability and the 95% confidence intervals (95% CI) of HIV-contamination risk in the female partners were calculated according to Clopper and Pearson.

Results

In the eight centres involved in this study, a total of 3390 assisted reproduction cycles were performed for 1036 couples. The number of cycles per couple varied from 1 to 19 (3.24 ± 2.58). Intra-uterine insemination was the most frequently used procedure (84%) (Table 2). The average age at the time of treatment was 32.3 years (range, 19-49) for female partners and 35.4 (range, 24-66) for the male partners.

Table 2. Results of assisted reproduction attempts according to the different procedures used.

FET, frozen embryo transfer; ICSI, intra cytoplasmic sperm injection; IUI, intra-uterine insemination; IVF, in-vitro fertilization.
aThe total was over 1036 couples as a couple could be have different assisted reproduction procedures (for example four IUI o two IVF).
bMissing information in 66 IUI and seven IVF cycles.
cMissing information in 91 IUI, 11 IVF and 40 ICSI cycles.
dP-value for comparison between procedure groups.


Previous pregnancies were reported for 219 (27%) of the 803 women for which this information was collected. These 219 women reported 272 pregnancies resulting in 149 terminations, 52 miscarriages and 65 deliveries. The latter were in 60 women. Previous pregnancy outcome was unknown for six women. Among the women who had previously delivered, 45 had 48 children with their current partner and these couples were now requesting assisted reproduction for a new pregnancy.

Three thousand, three hundred and ninety cycles of assisted reproduction with sperm washing were performed. In 75 cases the outcome of treatment was not known. Pregnancy resulted in 580 of the 3315 cycles where outcome was known (clinical pregnancy rate per cycle 17.5%; 95% CI, 16.2-18.8). Among the 1036 treated couples, 499 women were pregnant at least once (48.2%; 95% CI, 45.2-51.3). Three hundred and seventy were singleton pregnancies, 28 twin pregnancies and 25 were higher order multiple pregnancies for which two embryonic reductions were performed. The pregnancy order was not known for 157 pregnancies. Final outcome of pregnancy was not specified in 47 cases. Five hundred and thirty-three pregnancies resulted in 410 deliveries (80%): 368 singletons, 29 sets of twins (two neonatal deaths), 13 sets of triplets, resulting in 463 live births. One hundred and twelve miscarriages, eight extra-uterine pregnancies, two terminations of pregnancy and one intrauterine death occurred.

Nine hundred and sixty-seven out of 1036 women had a negative HIV test at least 6 months after their last assisted reproduction attempt with washed sperm. In 74 cases, the results of HIV testing in the female partner were unknown. Those lost to follow-up had attended the Italian centre amounting to 7.1% of all couples entered on the database.

In terms of treatment cycles performed, a negative HIV test was recorded 6 months post treatment in 3272 (96.5%) and no HIV test was recorded following the 124 (3.5%) cycles from 74 cases. No female seroconversion occurred following treatment in the 3272 cycles for which the results were known, allowing us to calculate the probability of contamination risk to be zero (95% CI, 0-0.09%).

Discussion
Prevention of HIV sexual transmission requires systematic use of condoms during intercourse. The consequence is to induce sterility in the couples. For this reason, numerous couples of reproductive age now seek medical assistance to have a child while minimizing the risk of infecting the HIV-negative partner.

For HIV-1-serodiscordant couples with an infected male partner, unprotected intercourse on the day of ovulation has been proposed and studies have analysed its safety. In 1997, Mandelbrot et al. reported four seroconversions, not related to the unprotected intercourse during ovulation, but occurring 7 months later or postpartum in a series of 92 natural conceptions in 92 HIV-1-negative women with an HIV-1-infected partner [5]. A more recent study [22] reported pregnancy and HIV-1 incidence in 178 married couples with discordant HIV-1 status. Women who became pregnant had a mean number of 8.4 acts of penetrative sex/month with 43% protected intercourse in comparison with a mean of 2.5 acts with 95% protected in women who did not become pregnant. One out of 14 women (7%) who became pregnant seroconverted and five out of 78 women who did not become pregnant seroconverted. It should be noted, however, that these two studies were done before the introduction of HAART or in a country were the HAART was not universally available.

In 1992, assisted reproduction with sperm washing was proposed in order to reduce the risk of female HIV contamination in HIV-1-serodiscordant couples [6]. Eight European centres offering assisted reproduction with sperm washing to HIV-1-serodiscordant couples have combined their results in this study. A total of 1036 couples underwent 3390 assisted reproduction cycles resulting in 580 pregnancies. No transmission of HIV to the female partner was observed after 3272 cycles with complete follow-up information. The upper level of the 95% CI of the transmission risk was thus 0.09%.

Several serodiscordant-couples studies have estimated that the risk of sexual HIV-1 transmission for a single act of penile-vaginal intercourse in a stable sexual partnership appears to be on the order of 0.1% (see Baeten and Overbaugh [19]). According to the De Vencenzi study [23] the calculated probability of women seroconverting was 0.1% (95% CI, 0.05-0.15) per natural intercourse [23]. Taking into account this hypothesis of contamination probability of 0.1% and that, according to the method published by Hanley and Lippman-Hand [24] we need 2275 cycles to demonstrate that the risk of female contamination during assisted reproduction is lower than during natural intercourse.
Accordingly, the number of assisted reproduction cycles in the present retrospective study without female contamination allows us to demonstrate the safety of the proposed assisted reproduction methods.

From a medical aspect, one must remember that couples search for a risk-reducing strategy in order to conceive. Moreover, a contrast exists between the calculated transmission risk during one act of sexual intercourse and the rate of female HIV-seroconversion reported for HIV-1-serodiscordant couples where the male partner is HIV-positive: four out of 92 couples (4.3%) in the Mandelbrot study [5], six out of 92 (6.5%) in the Ryder study [22]: and eight out of 74 (10.8%) in the De Vincenzi study [23] representing a total of 18 female seroconversions in a population of 268 (6.7%). In our study, we reported no seroconversions in the 967 women (P < 0.01) treated with washed sperm during assisted reproduction programmes.

Recently a case of seroconversion was reported in a woman preparing for assisted reproduction whose infected male partner was not under antiretroviral therapy [25].

It is noteworthy that the studies on transmission risk during unprotected intercourse were done either before HAART was available or in countries where it was unobtainable due to restricted resources. Blood viral load is known to increase the risk of seroconversion and HAART is known to reduce such risk [26]. It must, however, be remembered that several additional factors are associated with HIV-1 genome excretion in semen such as genital infection and inflammation and that HIV-1 genome has been found in a small proportion of men with undetectable blood viral load under HAART [27,28] while infectiousness in these cases was unknown.
The debate over the real risk of timed intercourse when the infected male has an undetectable viral load therefore continues. No seroconversions were observed in a more retrospective study of 77 HIV-1-serodiscordant couples who attempted conception through timed unprotected intercourse and in which the HIV-positive male partner had an undetectable blood viral load (< 500 copies/ml) through HAART [29]. This study did not, however, look for seroconversions in those couples who failed to conceive and the population size was too small to allow conclusions on the safety of this approach. Vernazza et al. have recently proposed additional measures to improve the safety of timed unprotected intercourse [30].

One limitation of our retrospective study was the loss to follow-up in 7.1% of couples. This loss to follow-up was due to geographical issues in the early days of the assisted reproduction programmes in the Italian centre. As these assisted reproduction programmes were offered to reduce the contamination risk, it is reasonable to presume that any female seroconversion following treatment would have been reported to the centre concerned.

The present study is the first multicentre study of the use of sperm washing in HIV-1-serodiscordant couples, in which the male partner was infected, who wished to conceive. It is the largest series published to date and the first with sufficient case numbers to confirm the safety and efficacy of assisted reproduction, where sperm washing was used as the primary means of avoiding HIV infection in the female partner. We recommend that public health authorities sustain and promote networks in order to analyse the results of assisted reproduction programmes, tailored to the needs of HIV-serodiscordant couples, and ensure a comprehensive database for the outcome of treatment and follow-up of all female patients treated is maintained, thereby facilitating epidemiologic studies.

According to our present data and other studies that have demonstrated the feasibility of such approach (see review by Gilling-Smith et al. [31]) it is neither ethically nor legally justifiable to exclude individuals from infertility services on the basis of male HIV-infection. For many countries in the world the first priority of the policy against HIV is to improve education, to allow access to HIV screening, to encourage condom use and to offer antiretroviral therapy where appropriate. In countries where these approaches are now in place we recommended that assisted reproductive programmes, such as IUI with sperm washing, should be integrated into a global public health initiative against HIV.



 
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





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Safety and efficacy of sperm washing in HIV-1-serodiscordant couples where the male is infected: results from the European CREAThE network

AIDS:Volume 21(14)September 2007p 1909-1914

Bujan, Louisa; Hollander, Litalb; Coudert, Mathieua; Gilling-Smith, Carolec; Vucetich, Alexandrab; Guibert, Julietted; Vernazza, Pietroe; Ohl, Jeaninef; Weigel, Michaelg; Englert, Yvonh; Semprini, Augusto Eb; for the CREAThE network
From the aUniversity Toulouse III Paul Sabatier, EA 3694, Research Group on Human Fertility and CECOS Midi-Pyrénées, Toulouse, France
bESMAN Medical Consulting, Milan, Italy
cDepartment of Obstetrics and Gynaecology, Chelsea & Westminster Hospital, London, UK
dAPHP, Hôpital Cochin - Université Paris Descartes, Unité de Médecine de la Reproduction Service de Gynécologie-obstétrique, Paris, France
eInfectious Diseases, Department of Medicine. Kantonsspital, St Gallen, Switzerland
fCentre d'AMP de Strasbourg, Service de Gynécologie-Obstétrique, CMCO-SIHCUS, Schiltigheim, France
gDepartment Obstetric and Gynaecology, University Hospital of Mannheim, Leopoldina-Krankenhaus, Schweinfurt, Germany
hFertility Clinic, Department of Obstetrics and Gynaecology, Erasme Hospital and Laboratory for Research in Human Reproduction, Medicine Faculty, Free University Brussels, Belgium.
*for REproductive Assistance Techniques for HIV in Europe.

“….A total of 580 pregnancies were obtained from 3315 cycles. Pregnancy outcome was unknown in 47 cases. The 533 pregnancies resulted in 410 deliveries and 463 live births. The result of female HIV testing after assisted reproduction was known in 967 out of 1036 woman (7.1% lost to follow-up). All tests recorded were negative. The calculated probability of contamination was equal to zero….

“….The present study is the first multicentre study of the use of sperm washing in HIV-1-serodiscordant couples, in which the male partner was infected, who wished to conceive. It is the largest series published to date and the first with sufficient case numbers to confirm the safety and efficacy of assisted reproduction, where sperm washing was used as the primary means of avoiding HIV infection in the female partner. We recommend that public health authorities sustain and promote networks in order to analyse the results of assisted reproduction programmes, tailored to the needs of HIV-serodiscordant couples, and ensure a comprehensive database for the outcome of treatment and follow-up of all female patients treated is maintained, thereby facilitating epidemiologic studies…..

…..According to our present data and other studies that have demonstrated the feasibility of such approach (see review by Gilling-Smith et al. [31]) it is neither ethically nor legally justifiable to exclude individuals from infertility services on the basis of male HIV-infection. For many countries in the world the first priority of the policy against HIV is to improve education, to allow access to HIV screening, to encourage condom use and to offer antiretroviral therapy where appropriate. In countries where these approaches are now in place we recommended that assisted reproductive programmes, such as IUI with sperm washing, should be integrated into a global public health initiative against HIV….”

Abstract
Objective: To examine the safety and effectiveness of assisted reproduction using sperm washing for HIV-1-serodiscordant couples wishing to procreate where the male partner is infected.

Design and methods: A retrospective multicentre study at eight centres adhering on the European network CREAThE and involving 1036 serodiscordant couples wishing to procreate. Sperm washing was used to obtain motile spermatozoa for
3390 assisted reproduction cycles (2840 intrauterine inseminations, 107 in-vitro fertilizations, 394 intra-cytoplasmic sperm injections and 49 frozen embryo transfers). An HIV test was performed in female partners at least 6 months after assisted reproduction attempt. The outcome measures recorded were number of assisted reproduction cycles, pregnancy outcome and HIV test on women post-treatment.

Results: A total of 580 pregnancies were obtained from 3315 cycles. Pregnancy outcome was unknown in 47 cases. The 533 pregnancies resulted in 410 deliveries and 463 live births. The result of female HIV testing after assisted reproduction was known in 967 out of 1036 woman (7.1% lost to follow-up).
All tests recorded were negative. The calculated probability of contamination was equal to zero (95% confidence interval, 0-0.09%).

Conclusion:
This first multicentre retrospective study of assisted reproduction following sperm washing demonstrates the method to be effective and to significantly reduce HIV-1 transmission risk to the uninfected female partner. These results support the view that assisted reproduction with sperm washing could not be denied to serodiscordant couples in developed countries and, where possible, could perhaps be integrated into a global public health initiative against HIV in developing countries.

Introduction
According to the latest UNAIDS/World Health Organization (WHO) update (December 2006), the total number of people living with HIV had reached 39.5 million. As the AIDS epidemic continues to take a massive and global toll on human lives, the call for comprehensive strategies to prevent HIV transmission has never been higher. A fundamental policy in halting the spread of HIV has been the encouragement and facilitation of condom use in vaginal and anal sexual contacts. This approach however raises a major dilemma for serodiscordant couples, where the male partner is infected, who wish to conceive. These couples form an increasing part of the HIV population in developed countries, where most individuals infected with HIV are of reproductive age and able to access effective antiretroviral treatment. Improved life expectancy and quality has enabled these individuals to reanalyse their future and consider parenting as a socially and ethically acceptable option and many now express the desire for parenthood [1-3] as a fundamental part of healthy family life and return to normality. Recently published guidelines from the American Society for Reproductive Medicine (ASRM) and ethics recommendations concerning assisted reproduction on people infected by virus have been modified to allow assisted reproduction in HIV-serodiscordant couples [4].

The desire to conceive could counteract preventive barrier methods such as condom use if couples do not receive sufficient information on reproductive options to reduce viral transmission risk. Adoption and assisted reproduction from donor sperm are two reproductive options available to couples which totally eliminate the risk of HIV transmission. However, both methods are not equally available throughout Europe and both deny the infected person a genetic link to his child and could reinforce feelings of stigma and discrimination. Unprotected intercourse restricted to the time of ovulation may limit the risk of HIV transmission but from the limited data available, transmission has been shown to occur under these conditions [5]. One way of allowing HIV-serodiscordant couples, where the male is infected, to conceive their biological children while limiting the risk of HIV transmission is the use of assisted reproduction after semen processing using the sperm washing method. Sperm washing, as a means of preventing female infection in HIV-1-serodiscordant couples where the male partner is infected, was first proposed 17 years ago at a time when no methods were available to detect HIV-1 nucleic acids in sperm and before the introduction of highly active antiretroviral treatment (HAART) [6]. Since then, several publications have reported the results of different sperm washing programmes in such couples [7-18].

The mean risk of sexual HIV-1 transmission for a single act of penile-vaginal intercourse appears to be on the order of 0.1% (see review by Bartin and Overbaugh [19]). Therefore, it is not easy to establish whether sperm washing and assisted reproduction actually reduces the risk of transmission in a significant way.

In Europe, centres involved in sperm washing programmes have created the CREAThE network (Centre for REproductive Assisted Techniques for HIV in Europe) whose primary objective is to pool knowledge, experience and results in order to improve the service offered to HIV-serodiscordant couples.

The present retrospective study analysed pooled data, from eight centres involved in the CREAThE network, to study the safety and efficacy of assisted reproduction with sperm washing in the largest series of sperm washing cases ever performed in serodiscordant couples where the male partner was HIV-1 positive.

Materials and methods
Eight centres from six European countries participated in retrospective data collection on assisted reproduction cycles performed between 1989 to 2003 (Table 1). Serodiscordant couples (n = 1036) in which the male partner was infected with HIV-1, attended the centres to follow a sperm washing programme. Variables concerning HIV-1 infection in the man, age of the woman at the time of treatment, and past gynaecological history were recorded from the patients' data in each centre. A fertility screen was performed for both partners. Sperm washing was performed according to published methods [6,9] with minor adaptations in each centre. Briefly, sperm washing has been previously reported using three steps: step 1, a spermatozoa migration on density gradient; step2, repeated washing of the migrated pellet, step 3, a spermatozoa swim up. Sperm washing was performed on one or more semen samples according to the protocol used in each centre. Briefly the sperm obtained after a recommended 3-7 days of abstinence was submitted to a separation following density gradient centrifugation. The 90% fraction was centrifuged and washed (method with two steps only) or submitted to a swim up method (method with three steps). The London, Strasbourg, Mannheim and Toulouse centres systematically performed the preparation with three steps and the Brussels and Milan centres also performed three steps except when there was a fertility issue where only the two-step method was performed. The St Gallen and Paris centres used only the two-step method and St Gallen used a specific double tube technique that has been reported [20]. The aim of all these sperm washing methods was to select only motile spermatozoa free of seminal plasma and semen cells such as leukocytes.

After its introduction into clinical use (1995-1997), HIV-1 genome detection was performed according to published methods [21] on the final fraction of spermatozoa obtained after sperm washing, except in the St Gallen centre where a more stringent separation method was used [20]. If HIV-1 RNA or DNA were not detected in the isolated spermatozoa fraction, fresh spermatozoa (Brussels, Milan, London) or frozen-thawed spermatozoa (Brussels, Milan, London, Paris, Strasbourg, Mannheim, Toulouse) fractions were used. Washed samples with detectable HIV-genomes were not used for assisted reproduction.

The assisted reproduction procedure choice (intra-uterine insemination (IUI), in-vitro fertilization (IVF) or intra-cytoplasmic sperm injection (ICSI)) was based on the result of the couple's fertility screen and each centre's protocols. Supernumerary embryos obtained after IVF or ICSI were frozen with the possibility of being transferred in a subsequent cycle (frozen embryo transfer; FET) if pregnancy did not occur after the first embryo transfer. Following each assisted reproduction cycle with washed sperm, HIV screening was performed on the female partners. The result of a HIV-test performed at least 6 months after the last assisted reproduction treatment was recorded in the database for this study.

Table 1. Patients and assisted reproduction cycles performed according to the centres involved on CREAThE network.

IUI, intra-uterine insemination; IVF, in-vitro fertilization; ICSI, intra cytoplasmic sperm injection; FET, frozen embryo transfer.
MPatients for whom the result of HIV test was unknown at least 6 months after the last assisted reproduction attempt.


All couples were required to systematically use condoms during intercourse throughout the period of treatment. They were informed about the assisted reproduction procedure and the fact that sperm washing may not totally eliminate transmission risk. All couples gave their informed consent to the assisted reproduction with sperm washing and the procedure was done in accordance with the declaration of Helsinki. In accordance with each country's laws, an agreement by an institutional review board was obtained. A limited number of anonymized clinical data for each patient from each centre were recorded in a central database and statistical analysis was performed using STATA software version 8.0 (StataCorp LP, College Station, Texas, USA). The probability and the 95% confidence intervals (95% CI) of HIV-contamination risk in the female partners were calculated according to Clopper and Pearson.

Results

In the eight centres involved in this study, a total of 3390 assisted reproduction cycles were performed for 1036 couples. The number of cycles per couple varied from 1 to 19 (3.24 ± 2.58). Intra-uterine insemination was the most frequently used procedure (84%) (Table 2). The average age at the time of treatment was 32.3 years (range, 19-49) for female partners and 35.4 (range, 24-66) for the male partners.

Table 2. Results of assisted reproduction attempts according to the different procedures used.

FET, frozen embryo transfer; ICSI, intra cytoplasmic sperm injection; IUI, intra-uterine insemination; IVF, in-vitro fertilization.
aThe total was over 1036 couples as a couple could be have different assisted reproduction procedures (for example four IUI o two IVF).
bMissing information in 66 IUI and seven IVF cycles.
cMissing information in 91 IUI, 11 IVF and 40 ICSI cycles.
dP-value for comparison between procedure groups.


Previous pregnancies were reported for 219 (27%) of the 803 women for which this information was collected. These 219 women reported 272 pregnancies resulting in 149 terminations, 52 miscarriages and 65 deliveries. The latter were in 60 women. Previous pregnancy outcome was unknown for six women. Among the women who had previously delivered, 45 had 48 children with their current partner and these couples were now requesting assisted reproduction for a new pregnancy.

Three thousand, three hundred and ninety cycles of assisted reproduction with sperm washing were performed. In 75 cases the outcome of treatment was not known. Pregnancy resulted in 580 of the 3315 cycles where outcome was known (clinical pregnancy rate per cycle 17.5%; 95% CI, 16.2-18.8). Among the 1036 treated couples, 499 women were pregnant at least once (48.2%; 95% CI, 45.2-51.3). Three hundred and seventy were singleton pregnancies, 28 twin pregnancies and 25 were higher order multiple pregnancies for which two embryonic reductions were performed. The pregnancy order was not known for 157 pregnancies. Final outcome of pregnancy was not specified in 47 cases. Five hundred and thirty-three pregnancies resulted in 410 deliveries (80%): 368 singletons, 29 sets of twins (two neonatal deaths), 13 sets of triplets, resulting in 463 live births. One hundred and twelve miscarriages, eight extra-uterine pregnancies, two terminations of pregnancy and one intrauterine death occurred.

Nine hundred and sixty-seven out of 1036 women had a negative HIV test at least 6 months after their last assisted reproduction attempt with washed sperm. In 74 cases, the results of HIV testing in the female partner were unknown. Those lost to follow-up had attended the Italian centre amounting to 7.1% of all couples entered on the database.

In terms of treatment cycles performed, a negative HIV test was recorded 6 months post treatment in 3272 (96.5%) and no HIV test was recorded following the 124 (3.5%) cycles from 74 cases. No female seroconversion occurred following treatment in the 3272 cycles for which the results were known, allowing us to calculate the probability of contamination risk to be zero (95% CI, 0-0.09%).

Discussion
Prevention of HIV sexual transmission requires systematic use of condoms during intercourse. The consequence is to induce sterility in the couples. For this reason, numerous couples of reproductive age now seek medical assistance to have a child while minimizing the risk of infecting the HIV-negative partner.

For HIV-1-serodiscordant couples with an infected male partner, unprotected intercourse on the day of ovulation has been proposed and studies have analysed its safety. In 1997, Mandelbrot et al. reported four seroconversions, not related to the unprotected intercourse during ovulation, but occurring 7 months later or postpartum in a series of 92 natural conceptions in 92 HIV-1-negative women with an HIV-1-infected partner [5]. A more recent study [22] reported pregnancy and HIV-1 incidence in 178 married couples with discordant HIV-1 status. Women who became pregnant had a mean number of 8.4 acts of penetrative sex/month with 43% protected intercourse in comparison with a mean of 2.5 acts with 95% protected in women who did not become pregnant. One out of 14 women (7%) who became pregnant seroconverted and five out of 78 women who did not become pregnant seroconverted. It should be noted, however, that these two studies were done before the introduction of HAART or in a country were the HAART was not universally available.

In 1992, assisted reproduction with sperm washing was proposed in order to reduce the risk of female HIV contamination in HIV-1-serodiscordant couples [6]. Eight European centres offering assisted reproduction with sperm washing to HIV-1-serodiscordant couples have combined their results in this study. A total of 1036 couples underwent 3390 assisted reproduction cycles resulting in 580 pregnancies. No transmission of HIV to the female partner was observed after 3272 cycles with complete follow-up information. The upper level of the 95% CI of the transmission risk was thus 0.09%.

Several serodiscordant-couples studies have estimated that the risk of sexual HIV-1 transmission for a single act of penile-vaginal intercourse in a stable sexual partnership appears to be on the order of 0.1% (see Baeten and Overbaugh [19]). According to the De Vencenzi study [23] the calculated probability of women seroconverting was 0.1% (95% CI, 0.05-0.15) per natural intercourse [23]. Taking into account this hypothesis of contamination probability of 0.1% and that, according to the method published by Hanley and Lippman-Hand [24] we need 2275 cycles to demonstrate that the risk of female contamination during assisted reproduction is lower than during natural intercourse.
Accordingly, the number of assisted reproduction cycles in the present retrospective study without female contamination allows us to demonstrate the safety of the proposed assisted reproduction methods.

From a medical aspect, one must remember that couples search for a risk-reducing strategy in order to conceive. Moreover, a contrast exists between the calculated transmission risk during one act of sexual intercourse and the rate of female HIV-seroconversion reported for HIV-1-serodiscordant couples where the male partner is HIV-positive: four out of 92 couples (4.3%) in the Mandelbrot study [5], six out of 92 (6.5%) in the Ryder study [22]: and eight out of 74 (10.8%) in the De Vincenzi study [23] representing a total of 18 female seroconversions in a population of 268 (6.7%). In our study, we reported no seroconversions in the 967 women (P < 0.01) treated with washed sperm during assisted reproduction programmes.

Recently a case of seroconversion was reported in a woman preparing for assisted reproduction whose infected male partner was not under antiretroviral therapy [25].

It is noteworthy that the studies on transmission risk during unprotected intercourse were done either before HAART was available or in countries where it was unobtainable due to restricted resources. Blood viral load is known to increase the risk of seroconversion and HAART is known to reduce such risk [26]. It must, however, be remembered that several additional factors are associated with HIV-1 genome excretion in semen such as genital infection and inflammation and that HIV-1 genome has been found in a small proportion of men with undetectable blood viral load under HAART [27,28] while infectiousness in these cases was unknown.
The debate over the real risk of timed intercourse when the infected male has an undetectable viral load therefore continues. No seroconversions were observed in a more retrospective study of 77 HIV-1-serodiscordant couples who attempted conception through timed unprotected intercourse and in which the HIV-positive male partner had an undetectable blood viral load (< 500 copies/ml) through HAART [29]. This study did not, however, look for seroconversions in those couples who failed to conceive and the population size was too small to allow conclusions on the safety of this approach. Vernazza et al. have recently proposed additional measures to improve the safety of timed unprotected intercourse [30].

One limitation of our retrospective study was the loss to follow-up in 7.1% of couples. This loss to follow-up was due to geographical issues in the early days of the assisted reproduction programmes in the Italian centre. As these assisted reproduction programmes were offered to reduce the contamination risk, it is reasonable to presume that any female seroconversion following treatment would have been reported to the centre concerned.

The present study is the first multicentre study of the use of sperm washing in HIV-1-serodiscordant couples, in which the male partner was infected, who wished to conceive. It is the largest series published to date and the first with sufficient case numbers to confirm the safety and efficacy of assisted reproduction, where sperm washing was used as the primary means of avoiding HIV infection in the female partner. We recommend that public health authorities sustain and promote networks in order to analyse the results of assisted reproduction programmes, tailored to the needs of HIV-serodiscordant couples, and ensure a comprehensive database for the outcome of treatment and follow-up of all female patients treated is maintained, thereby facilitating epidemiologic studies.

According to our present data and other studies that have demonstrated the feasibility of such approach (see review by Gilling-Smith et al. [31]) it is neither ethically nor legally justifiable to exclude individuals from infertility services on the basis of male HIV-infection. For many countries in the world the first priority of the policy against HIV is to improve education, to allow access to HIV screening, to encourage condom use and to offer antiretroviral therapy where appropriate. In countries where these approaches are now in place we recommended that assisted reproductive programmes, such as IUI with sperm washing, should be integrated into a global public health initiative against HIV.






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#22699 From: Nelson Vergel <nelsonvergel@...>
Date: Fri Aug 31, 2007 2:36 pm
Subject: Re: Jaundice with Reyataz
nelsonvergel
Offline Offline
Send Email Send Email
 
Dear John

You said you had high lips with Atripla (it can happen), then switched to boosted Reyataz and had jaundice (it happens).  I am assuming that you have not have developed resistance to either Sustiva, Reyataz, Viread and Emtriva.

Depending on your CD4 cells at start and assuming that you have undetectable  (under 50) viral load, you can safely switch to Viramune plus Truvada. This combo does not cause jaundice and it is known to be lipid friendly.  You can develop a rash that your doctor can manage.  Men with CD4 cells over 400 at baseline have shown increases in liver enzymes, but this problem does not seem to be as bad for those who start HAART following current guidelines of 350 CD4 or less. Also, in a recent study, those taking a previous HAART regimen who had undetectable viral load and high CD4 cells (over 400) were able to switch safely to Viramune without any liver problems.
 
Regards,
 
Nelson Vergel
powerusa dot org


----- Original Message ----
From: lo lo <speciman70@...>
To: John R. Cook <johnca51@...>; PozHealth@yahoogroups.com
Sent: Friday, August 31, 2007 2:48:21 AM
Subject: Re: [PozHealth] Jaundice

Hey John,
I've been on this regimen for months now. Give your body - your liver for that matter - time to adjust, and this will go away in no time.
I'm not a doc, but I'm concerned about yours lowering your dose. Isn't dangerous to do so, and doesn't it increase the risk of building resistance ? Reyataz is well known for causing this side effect, and again, you shouldn't worry to much about it. It takes only a few weeks before it disappears. Plus, it is an excellent regimen that has proven is effectiveness over time. Hope this will help.
Best to all the Poz readers.
Laurent from Paris, France.


"John R. Cook" <johnca51@...> wrote:
Hi Guys and Girls;
I read a message from someone about his partner with Cushing's Syndrome
and became jaundice after starting Reyataz and Norvir. I had alot of
reservations starting Reyataz and Norvir after reading that message,
since I also have Cushing's Syndrome, but my Trigiycerides were way to
high on Sustiva/Atripla.
I started Reyataz, Norvir, and Truvada and Aug 9th and on Sunday the
26th I woke up jundice!!! Went to my PMD and he adjusted my meds to a
lower does. Well I hepe this works. Any encouragement or advice?
Thanks, John R. Cook



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#22698 From: "marc_jaffeux" <marc.jaffeux@...>
Date: Fri Aug 31, 2007 12:10 pm
Subject: Re: Jaundice
marc_jaffeux
Offline Offline
Send Email Send Email
 
Hello,

Do you take any other drugs containing cortisone ? Cushing's Syndrome
is an intoxication due to an overdose of cortisone. Norvir boost the
level of cortisone in blood. So, if you take any drugs containing
cortisone AND Norvir, you should very carefully dose cortisone' level
in blood, every month. Anyway, it is safer not to associate Norvir
with cortisone.

For example :
There have been serious Cushing's Syndromes due to an interaction
between Norvir and a drug against asthma called Seretide, containing
cortisone. Seretide (fluticasone) is to be inhale. It should stay on
the lung, and not go in the blood (GSK says). In fact, it does go a
little into blood, and can induce a Cushing syndrome (my friend had
one). A poster has been published about it, two years ago. I couldn't
find the data itself on internet : _Syndrome de cushing iatrogne li
 l'interaction entre le ritonavir et la fluticasone chez des patients
infects par le VIH traits par corticodes inhals : description de 4
cas. N. Valin, V. Garrait, N. De Castro, J.-M. Molina._

Cushing's syndrome can lower DHEA level in the blood. This hormone is
important for bones preservation. Maybe you should dose DHEA in your
blood, and, if too low, take a supplementation of it.

I hope all goes well for you.

All the best

Marc,
France

--- In PozHealth@yahoogroups.com, "John R. Cook" <johnca51@...> wrote:
>
> Hi Guys and Girls;
> I read a message from someone about his partner with Cushing's Syndrome
> and became jaundice after starting Reyataz and Norvir.  I had alot of
> reservations starting Reyataz and Norvir after reading that message,
> since I also have Cushing's Syndrome, but my Trigiycerides were way to
> high on Sustiva/Atripla.
> I started Reyataz, Norvir, and Truvada and Aug 9th and on Sunday the
> 26th I woke up jundice!!!  Went to my PMD and he adjusted my meds to a
> lower does.  Well I hepe this works.  Any encouragement or advice?
> Thanks, John R. Cook
>

#22697 From: JuLev@...
Date: Fri Aug 31, 2007 5:42 am
Subject: NATAP: Risk of Cancers in SMART
jules72orange
Offline Offline
Send Email Send Email
 
Risk of cancers during interrupted antiretroviral therapy in the SMART study (08/30/07)


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#22696 From: lo lo <speciman70@...>
Date: Fri Aug 31, 2007 7:48 am
Subject: Re: Jaundice
speciman70
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Hey John,
I've been on this regimen for months now. Give your body - your liver for that matter - time to adjust, and this will go away in no time.
I'm not a doc, but I'm concerned about yours lowering your dose. Isn't dangerous to do so, and doesn't it increase the risk of building resistance ? Reyataz is well known for causing this side effect, and again, you shouldn't worry to much about it. It takes only a few weeks before it disappears. Plus, it is an excellent regimen that has proven is effectiveness over time. Hope this will help.
Best to all the Poz readers.
Laurent from Paris, France.


"John R. Cook" <johnca51@...> wrote:
Hi Guys and Girls;
I read a message from someone about his partner with Cushing's Syndrome
and became jaundice after starting Reyataz and Norvir. I had alot of
reservations starting Reyataz and Norvir after reading that message,
since I also have Cushing's Syndrome, but my Trigiycerides were way to
high on Sustiva/Atripla.
I started Reyataz, Norvir, and Truvada and Aug 9th and on Sunday the
26th I woke up jundice!!! Went to my PMD and he adjusted my meds to a
lower does. Well I hepe this works. Any encouragement or advice?
Thanks, John R. Cook



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#22695 From: JuLev@...
Date: Fri Aug 31, 2007 5:14 am
Subject: Re: Over one year of 3TC use associated with increased risk of diabetes for HIV-posi
jules72orange
Offline Offline
Send Email Send Email
 

In a message dated 8/30/07 7:49:32 PM, PoWeRTX@... writes:


I have never heard of toxicities associated with 3TC compared to other nukes...
We always assume that Epivir (3TC) has little mitochondrial toxicity. Interesting....



Here is link to the full text of this article in AIDS where they concluded: c
umulative exposure to NRTI, but not PI or NNRTI, was associated with increased DM incidence, using the definition stated in our methods--

ART exposure and incidence of diabetes mellitus in the Women's Interagency HIV Study: NRTI but not PI nor NNRTI associated with diabetes - (08/15/07)


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#22694 From: "John R. Cook" <johnca51@...>
Date: Fri Aug 31, 2007 12:10 am
Subject: Jaundice
johnca51
Offline Offline
Send Email Send Email
 
Hi Guys and Girls;
I read a message from someone about his partner with Cushing's Syndrome
and became jaundice after starting Reyataz and Norvir.  I had alot of
reservations starting Reyataz and Norvir after reading that message,
since I also have Cushing's Syndrome, but my Trigiycerides were way to
high on Sustiva/Atripla.
I started Reyataz, Norvir, and Truvada and Aug 9th and on Sunday the
26th I woke up jundice!!!  Went to my PMD and he adjusted my meds to a
lower does.  Well I hepe this works.  Any encouragement or advice?
Thanks, John R. Cook

#22693 From: George Carter <fiar@...>
Date: Thu Aug 30, 2007 10:07 pm
Subject: Sorta off topic
lalzephyr
Offline Offline
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I was wondering if anyone has extra Kaletra - maybe 10-12 softgels
(or tablets?)...

A friend's kitten has a coronaviral infection that causes enlarged
liver (hepatomegaly). This causes Feline Infectious Peritonitis (FIP)
which has a very poor prognosis. The kitten eats well and is
otherwise healthy (that is, kidneys, other organs good, defecates and
urinates OK; however, has a bit of wasting and is thin with distended
belly due to the ascites).

Interestingly, SARS, caused by another kind of coronavirus found in
civets, responds to lopinavir/ritonavir. Acyclovir doesn't work
apparently (just one in vitro study) and ribavirin is too toxic for
cats.

We've got him on a lot of liver supportive therapy, ascites have been
drained, he'll be getting a low dose of prednisolone.

But I thought, this could be a what the hell idea that might save the
kittens life.

If anyone has extra that they ABSOLUTELY OTHERWISE DO NOT NEED,
please drop me an email.
Thanks!!
George M. Carter

#22692 From: Jonathan Goldman <yangzpa@...>
Date: Thu Aug 30, 2007 8:03 pm
Subject: The Houston HIV Katrina
yangzpa
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Regarding the issue one person posted about continuing with a doctor
doing this 'gold service' at a fee because of a continuing clinical
trial....I suppose, if it's an expanded access medication, that could
be 'easily' moved to another practice, that might be the way to go.
However, if it's a true clinical study- there is paperwork that each
participant was given at the beginning to show the sponsoring agency.
And, each study has some type of Institutional Review Board or
Community Advisory Board that could/should be made aware that a
participating doctor will be charging patients already enrolled a
special fee to continue seeing that doctor. I don't believe that NIH
or the pharma industry would want to see people leaving a study
because the MD has instituted a surcharge....Just my thoughts before
heading off on vacation for two weeks. Take care eveyone!

Healthfully & electronically,
      Jonathan "Gravy Boat" Goldman
         Project Inform Hotline Manager
            415.558.8669, x215
         National HIV/AIDS Treatment Hotline 800.822-7422
             jgoldman@... / www.projectinform.org


"Better to remain silent and be thought a fool than to speak out and remove all
doubt."
attributed to Abraham Lincoln

#22691 From: bgmaron <bgmaron@...>
Date: Thu Aug 30, 2007 8:54 pm
Subject: Enrollment Fee RE: Houston HIV Katrina
bgmaron
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I heard that physical doctors is going charge " enrollment fee" such $1,500 , 2,000 , 3,000  a year. I afraid if it is going spread that new system around the country  because Medicaids and insurances won't pay in advance so  Doctors get lose of patience for paperworks and money from clients, insurances. is that new trendy for 2008?
Mark


Mark

#22690 From: PoWeRTX@...
Date: Thu Aug 30, 2007 2:29 pm
Subject: Over one year of 3TC use associated with increased risk of diabetes for HIV-posi
nelsonvergel
Offline Offline
Send Email Send Email
 
I have never heard of toxicities associated with 3TC compared to other nukes...
We always assume that Epivir (3TC) has little mitochondrial toxicity. Interesting....
 
 
Over one year of 3TC use associated with increased risk of diabetes for HIV-positive women
Wednesday, August 29, 2007
The investigators speculate that “NRTI-induced mitochondrial dysfunction” could be contributing to the development of diabetes.

By Michael Carter

Cumulative nucleoside reverse transcriptase inhibitor (NRTI) use, particularly 3TC (lamivudine, Epivir) is associated with an increased risk of type 2 diabetes in HIV-positive women, according to a US study published in the August 28th edition of AIDS.

The investigators speculate that “NRTI-induced mitochondrial dysfunction” could be contributing to the development of diabetes. By contrast, neither protease inhibitor treatment, nor treatment with non-nucleoside reverse transcriptase inhibitors use (NNRTIs) were associated with the development of diabetes mellitus.

Diabetes mellitus has been a concern for HIV-infected individuals since reports emerged implicating protease inhibitors in the development of glucose intolerance and insulin resistance.

Studies demonstrating an association between antiretroviral treatment and the development of heart disease have intensified the need to clarify the relationship between anti-HIV therapy and diabetes mellitus as diabetes is a primary risk factor for cardiovascular illness.

Earlier studies looking at the association between antiretroviral therapy and diabetes mellitus have been limited by the small number of cases reported, their reliance on self-report, or the lack of an HIV-negative comparator group.

Investigators from the prospective Women’s Interagency HIV Study (WIHS), which includes HIV-positive women and women with a risk of HIV infection, followed 2,088 women for five and a half years to determine the incidence of diabetes mellitus and its association with anti-HIV therapy.

The study included 1,524 HIV-positive women and 564 HIV-negative women. At three-monthly intervals between 2000 and 2006 they had their fasting glucose monitored and the HIV-infected women provided information on the use of antiretroviral drugs.

Women with fasting glucose above 1.26mg/l, or who were prescribed diabetes medication, were classified as having incident diabetes mellitus. Body measurements were taken at baseline and throughout the study, and before entry to the study, the women were questioned about the presence of traditional risk-factors for diabetes.

HIV-positive and HIV-negative women were well-matched on entry to the study, although HIV-positive women were significantly older (39 versus 34 years, p < 0.001), had a lower body mass index (27kg/m2 versus 28 kg/m2, p = 0.001), a lower median hip size (99cm versus 102cm, p < 0.001), and were more likely to be menopausal (17% versus 9%, p < 0.001), and to be coinfected with hepatitis C virus (30% versus 16%, p < 0.001) than HIV-negative women.

Median fasting glucose was 830mg/l, and was the same in HIV-positive and -negative women. During follow-up, a total of 152 incident cases of diabetes mellitus were diagnosed, 116 of which were in women with HIV.

Compared with the diabetes mellitus incidence rate in HIV-negative women (1.96 per 100 person-years), HIV-positive women not taking anti-HIV therapy had a lower incidence rate of 1.53 per 100 person-years. The incidence rate was higher for women taking one or two drug anti-HIV treatment (3.40 per 100 person-years). For women taking protease inhibitor-containing anti-HIV therapy, the incident rate was 2.5 per 100 person years, and for women taking potent anti-HIV therapy that did not include a protease inhibitor, the incidence rate was 2.89 per 100 person years.

In adjusted statistical analysis, none of the associations between treatment group and diabetes mellitus were significant.

However, the investigators found that longer cumulative exposure to NRTI drugs was associated with an increased risk of diabetes mellitus compared to no NRTI use (relative hazard [RH], 1.81; 95% CI, 0.83 – 3.93 for zero to three years of NRTI treatment with a RH of 2.64; 95% CI, 1.11 – 6.32, for over three years of NRTI exposure).

Neither cumulative exposure to protease inhibitors, nor cumulative exposure to NNRTIs was found to be associated with the development of diabetes mellitus.

In further analysis, of the four most commonly used NRTIs (AZT, abacavir, d4T and 3TC), only cumulative exposure to 3TC was found to be significantly associated with an increased risk of diabetes mellitus (over one year of 3TC exposure, adjusted RH, 2.81; 95% CI, 1.33 – 5.95).

“We conclude that cumulative exposure to NRTI, but not PI or NNRTI, was associated with increased diabetes mellitus incidence”, write the investigators. They add, “NRTI remain the backbone of effective antiretroviral therapy, and so regular monitoring of fasting glucose levels in HIV-infected patients is warranted. Study of the biological mechanisms by which NRTI might induce disorders in glucose metabolism is a priority.”


Reference
Tien PC et al. Antiretroviral therapy exposure and incidence of diabetes mellitus in the Women’s Interagency HIV Study. AIDS 21: 1739 – 1745, 2007.


SOURCE: Aidsmap
http://www.aidsmap.com/en/news/C494A67B-7A6E-412D-927B-DDAB4...
Regards,

Nelson Vergel
Program for Wellness Restoration
PoWeRUSA dot org


“I had rather attempt something great and fail, than to attempt nothing at all and succeed.” R. Schuller





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#22689 From: "jim98122x" <jim98122x@...>
Date: Thu Aug 30, 2007 6:15 pm
Subject: Re: The Houston HIV Katrina
jim98122x
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"Rapidly approaching?"   That's  a joke, we've been there for years.  Millions of people already have no health insurance, and rely on public health trust hospitals (or no care at all).  If that's not "two tiered", what is?   This would be THREE tiered. 

Hell, why stop at three tiered?  While we're at it, why don't we put into place something like airlines frequent flyer programs?  We can have a whole range of priority levels assigned to the worth of you as a person.  If you're waiting for your doctor and you're, say,  only "bronze level", and a "gold elite" patient comes in, they bump you aside, take priority, and you wait longer.  I know I've gone to see my doc when I had no appointment and had to wait while they fit me in "space available".  Why not just start assigning levels of importance and let people get "bumped"?  This program already does that-- the level of importance is tied directly to one parameter-- money.  Isn't that nice?  A heartwarming validation of the Hippocratic oath.


--- In PozHealth@yahoogroups.com, "george vowell" <dvowell@...> wrote:
>
> It seems that we are rapidly approaching what other countries already have. That is, two tiered medical coverage. As long as no one goes without a competent doctor, it is not unreasonable for doctors to limit their practice in order to provide optimal treatment to a set number of patients. A philanthropical doctor would/should leave room for a percentage of patients that cannot afford to pay for such "blue ribbon" treatment. Just my opinion.
>
> Dave Vowell
>


#22688 From: PoWeRTX@...
Date: Thu Aug 30, 2007 9:58 am
Subject: Section 2257 Docket No. CRM 104
nelsonvergel
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To: Admin.ceos@...
Re: Section 2257 Docket No. CRM 104

To the U.S. Department of Justice:

I am writing to object to the proposed “Section 2257” regulations.

These regulations are complicated and burdensome on legitimate businesses, and have very little to do with protecting children and minors from pornography. Their reach — particularly into adult social-networking internet services — is overbroad, unnecessary, and would allow the federal government to search and seize personal records of adult consumers without a warrant; a clear violation privacy and constitutional rights.

Specifically, I object to the following provisions:

1. The regulations (18 § 2257(b)(1) and (c)) would force adult social-networking services to obtain and maintain personal information about their users, including the user's photo ID (driver’s license, passport, or military ID). (I must note that the sites already require users to affirm that they are over 18 years of age.) Many sites have tens of thousands of users and it is simply not possible for them to do this. Moreover, many people who use these sites want to maintain their privacy, for any number of reasons, including the sad fact that they might face discrimination and/or violence if others found out they were using these sites. It is still legal in 31 states to discriminate against someone who is gay or bisexual, and in 41 states if the person is transgender. The combination of the recordkeeping requirements and many users’ fears about providing such information will kill the entire industry.

All of this is overkill given that adult social networking sites were not identified as a problem in the production, distribution and downloading of child pornography in the Department of Justice’s own report on “Child Pornography on the Internet” (May 2006).

2. The regulations (18 § 2257(g) and under 28 C.F.R. § 75.5) would allow the Attorney General to conduct unannounced warrantless searches at will on the sites’ records, including reviewing and presumably seizing the personal information on site users. This is an egregious abuse of government authority, an unwarranted invasion of privacy and, in my opinion, a violation of the Fourth Amendment of the U.S. Constitution.

3. The regulations (28 C.F.R. § 75.5(4)) provide insufficient safeguards over what the government can do with the information it obtains through its searches. This, by itself, has a chilling effect on the ability of people to engage in constitutionally protected activities. As noted above, this is particularly dangerous for gay, lesbian, bisexual and transgender people.

Let me be clear: I believe children need to be protected from coercion into pornography and it is important for the federal government to do all that it can to insure those protections. Sadly, many of the provisions of the proposed 2257 regulations do nothing to address child pornography, but instead are clearly aiming at destroying an industry and ending a legal and valuable way for adults to meet one another.

 
Regards,

Nelson Vergel




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#22687 From: "Sanford Gross" <SGross@...>
Date: Thu Aug 30, 2007 2:35 pm
Subject: Re: The Houston HIV Katrina
SGross@...
Send Email Send Email
 
In medicine, what is optimal treatment? and who should get the
sub-optimal variety?  A two-tiered fee system is explicitly technically
illegal, at least in Illinois. Does this mean I can spend less time,
effort, and and compassion on behalf of my Medicaid versus self-pay
patients?

You are essntially making a deal with the devil and opening the door to
discimination against the impoverished yet once more.

In my opinion, it is not Ok and I would make sure my community sent
that doctor a very clear message. That is, if he has a conscience to
which you can even appeal.

We take oatths when we graduate that is very specific about
discrimination on the basis of.......

Sanford

Sanford M. Gross, OD, FAAO
Associate Professor
Illinois College of Optometry
3241 South Michigan Ave
Chicago, Illinois 60616

>>> "george vowell" <dvowell@...> 08/30/07 8:30 AM >>>
     It seems that we are rapidly approaching what other countries
already have. That is, two tiered medical coverage. As long as no one
goes without a competent doctor, it is not unreasonable for doctors to
limit their practice in order to provide optimal treatment to a set
number of patients. A philanthropical doctor would/should leave room for
a percentage of patients that cannot afford to pay for such "blue
ribbon" treatment. Just my opinion.

Dave Vowell
BEGIN:VCARD
VERSION:2.1
X-GWTYPE:USER
FN:Sanford Gross
TEL;WORK:x7314
ORG:;Primary Care
EMAIL;WORK;PREF;NGW:SGross@...
N:Gross;Sanford
END:VCARD

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