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  3. Hormonal Contraception and the Risk of HIV Acquisition: An Individual Participant Data Meta-analysis.
 

Hormonal Contraception and the Risk of HIV Acquisition: An Individual Participant Data Meta-analysis.

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BORIS DOI
10.7892/boris.62774
Date of Publication
January 2015
Publication Type
Article
Division/Institute

Institut für Sozial- ...

Contributor
Morrison, Charles S
Chen, Pai-Lien
Kwok, Cynthia
Baeten, Jared M
Brown, Joelle
Crook, Angela M
Van Damme, Lut
Delany-Moretlwe, Sinead
Francis, Suzanna C
Friedland, Barbara A
Hayes, Richard J
Heffron, Renee
Kapiga, Saidi
Karim, Quarraisha Abdool
Karpoff, Stephanie
Kaul, Rupert
McClelland, R Scott
McCormack, Sheena
McGrath, Nuala
Myer, Landon
Rees, Helen
van der Straten, Ariane
Watson-Jones, Deborah
van de Wijgert, Janneke H H M
Stalter, Randy
Low, Nicolaorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
PLoS medicine
ISSN or ISBN (if monograph)
1549-1277
Publisher
Public Library of Science
Language
English
Publisher DOI
10.1371/journal.pmed.1001778
PubMed ID
25612136
Description
BACKGROUND

Observational studies of a putative association between hormonal contraception (HC) and HIV acquisition have produced conflicting results. We conducted an individual participant data (IPD) meta-analysis of studies from sub-Saharan Africa to compare the incidence of HIV infection in women using combined oral contraceptives (COCs) or the injectable progestins depot-medroxyprogesterone acetate (DMPA) or norethisterone enanthate (NET-EN) with women not using HC.

METHODS AND FINDINGS

Eligible studies measured HC exposure and incident HIV infection prospectively using standardized measures, enrolled women aged 15-49 y, recorded ≥15 incident HIV infections, and measured prespecified covariates. Our primary analysis estimated the adjusted hazard ratio (aHR) using two-stage random effects meta-analysis, controlling for region, marital status, age, number of sex partners, and condom use. We included 18 studies, including 37,124 women (43,613 woman-years) and 1,830 incident HIV infections. Relative to no HC use, the aHR for HIV acquisition was 1.50 (95% CI 1.24-1.83) for DMPA use, 1.24 (95% CI 0.84-1.82) for NET-EN use, and 1.03 (95% CI 0.88-1.20) for COC use. Between-study heterogeneity was mild (I2 < 50%). DMPA use was associated with increased HIV acquisition compared with COC use (aHR 1.43, 95% CI 1.23-1.67) and NET-EN use (aHR 1.32, 95% CI 1.08-1.61). Effect estimates were attenuated for studies at lower risk of methodological bias (compared with no HC use, aHR for DMPA use 1.22, 95% CI 0.99-1.50; for NET-EN use 0.67, 95% CI 0.47-0.96; and for COC use 0.91, 95% CI 0.73-1.41) compared to those at higher risk of bias (pinteraction = 0.003). Neither age nor herpes simplex virus type 2 infection status modified the HC-HIV relationship.

CONCLUSIONS

This IPD meta-analysis found no evidence that COC or NET-EN use increases women's risk of HIV but adds to the evidence that DMPA may increase HIV risk, underscoring the need for additional safe and effective contraceptive options for women at high HIV risk. A randomized controlled trial would provide more definitive evidence about the effects of hormonal contraception, particularly DMPA, on HIV risk.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/129012
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