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No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis

OBJECTIVE: Preexposure prophylaxis (PrEP) with emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) reduced HIV acquisition in the iPrEx trial among men who have sex with men and transgender women. Self-reported sexual risk behavior decreased overall, but may be affected by reporting bias. We evalu...

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Autores principales: Marcus, Julia L., Glidden, David V., Mayer, Kenneth H., Liu, Albert Y., Buchbinder, Susan P., Amico, K. Rivet, McMahan, Vanessa, Kallas, Esper Georges, Montoya-Herrera, Orlando, Pilotto, Jose, Grant, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867330/
https://www.ncbi.nlm.nih.gov/pubmed/24367497
http://dx.doi.org/10.1371/journal.pone.0081997
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author Marcus, Julia L.
Glidden, David V.
Mayer, Kenneth H.
Liu, Albert Y.
Buchbinder, Susan P.
Amico, K. Rivet
McMahan, Vanessa
Kallas, Esper Georges
Montoya-Herrera, Orlando
Pilotto, Jose
Grant, Robert M.
author_facet Marcus, Julia L.
Glidden, David V.
Mayer, Kenneth H.
Liu, Albert Y.
Buchbinder, Susan P.
Amico, K. Rivet
McMahan, Vanessa
Kallas, Esper Georges
Montoya-Herrera, Orlando
Pilotto, Jose
Grant, Robert M.
author_sort Marcus, Julia L.
collection PubMed
description OBJECTIVE: Preexposure prophylaxis (PrEP) with emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) reduced HIV acquisition in the iPrEx trial among men who have sex with men and transgender women. Self-reported sexual risk behavior decreased overall, but may be affected by reporting bias. We evaluated potential risk compensation using biomarkers of sexual risk behavior. DESIGN AND METHODS: Sexual practices were assessed at baseline and quarterly thereafter; perceived treatment assignment and PrEP efficacy beliefs were assessed at 12 weeks. Among participants with ≥1 follow-up behavioral assessment, sexual behavior, syphilis, and HIV infection were compared by perceived treatment assignment, actual treatment assignment, and perceived PrEP efficacy. RESULTS: Overall, acute HIV infection and syphilis decreased during follow-up. Compared with participants believing they were receiving placebo, participants believing they were receiving FTC/TDF reported more receptive anal intercourse partners prior to initiating drug (12.8 vs. 7.7, P = 0.04). Belief in receiving FTC/TDF was not associated with an increase in receptive anal intercourse with no condom (ncRAI) from baseline through follow-up (risk ratio [RR] 0.9, 95% confidence interval [CI]: 0.6–1.4; P = 0.75), nor with a decrease after stopping study drug (RR 0.8, 95% CI: 0.5–1.3; P = 0.46). In the placebo arm, there were trends toward lower HIV incidence among participants believing they were receiving FTC/TDF (incidence rate ratio [IRR] 0.8, 95% CI: 0.4–1.8; P = 0.26) and also believing it was highly effective (IRR 0.5, 95% CI: 0.1–1.7; P = 0.12). CONCLUSIONS: There was no evidence of sexual risk compensation in iPrEx. Participants believing they were receiving FTC/TDF had more partners prior to initiating drug, suggesting that risk behavior was not a consequence of PrEP use.
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spelling pubmed-38673302013-12-23 No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis Marcus, Julia L. Glidden, David V. Mayer, Kenneth H. Liu, Albert Y. Buchbinder, Susan P. Amico, K. Rivet McMahan, Vanessa Kallas, Esper Georges Montoya-Herrera, Orlando Pilotto, Jose Grant, Robert M. PLoS One Research Article OBJECTIVE: Preexposure prophylaxis (PrEP) with emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) reduced HIV acquisition in the iPrEx trial among men who have sex with men and transgender women. Self-reported sexual risk behavior decreased overall, but may be affected by reporting bias. We evaluated potential risk compensation using biomarkers of sexual risk behavior. DESIGN AND METHODS: Sexual practices were assessed at baseline and quarterly thereafter; perceived treatment assignment and PrEP efficacy beliefs were assessed at 12 weeks. Among participants with ≥1 follow-up behavioral assessment, sexual behavior, syphilis, and HIV infection were compared by perceived treatment assignment, actual treatment assignment, and perceived PrEP efficacy. RESULTS: Overall, acute HIV infection and syphilis decreased during follow-up. Compared with participants believing they were receiving placebo, participants believing they were receiving FTC/TDF reported more receptive anal intercourse partners prior to initiating drug (12.8 vs. 7.7, P = 0.04). Belief in receiving FTC/TDF was not associated with an increase in receptive anal intercourse with no condom (ncRAI) from baseline through follow-up (risk ratio [RR] 0.9, 95% confidence interval [CI]: 0.6–1.4; P = 0.75), nor with a decrease after stopping study drug (RR 0.8, 95% CI: 0.5–1.3; P = 0.46). In the placebo arm, there were trends toward lower HIV incidence among participants believing they were receiving FTC/TDF (incidence rate ratio [IRR] 0.8, 95% CI: 0.4–1.8; P = 0.26) and also believing it was highly effective (IRR 0.5, 95% CI: 0.1–1.7; P = 0.12). CONCLUSIONS: There was no evidence of sexual risk compensation in iPrEx. Participants believing they were receiving FTC/TDF had more partners prior to initiating drug, suggesting that risk behavior was not a consequence of PrEP use. Public Library of Science 2013-12-18 /pmc/articles/PMC3867330/ /pubmed/24367497 http://dx.doi.org/10.1371/journal.pone.0081997 Text en © 2013 Marcus et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Marcus, Julia L.
Glidden, David V.
Mayer, Kenneth H.
Liu, Albert Y.
Buchbinder, Susan P.
Amico, K. Rivet
McMahan, Vanessa
Kallas, Esper Georges
Montoya-Herrera, Orlando
Pilotto, Jose
Grant, Robert M.
No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis
title No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis
title_full No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis
title_fullStr No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis
title_full_unstemmed No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis
title_short No Evidence of Sexual Risk Compensation in the iPrEx Trial of Daily Oral HIV Preexposure Prophylaxis
title_sort no evidence of sexual risk compensation in the iprex trial of daily oral hiv preexposure prophylaxis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867330/
https://www.ncbi.nlm.nih.gov/pubmed/24367497
http://dx.doi.org/10.1371/journal.pone.0081997
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