Risk of HIV-1 acquisition among women who use different types of injectable progestin contraception in South Africa: a prospective cohort study

Summary Background Several observational studies have reported that HIV-1 acquisition seems to be higher in women who use depot medroxyprogesterone acetate (DMPA) than in those who do not use hormonal contraception. We aimed to assess whether two injectable progestin-only contraceptives, DMPA and no...

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Veröffentlicht in:The lancet HIV 2015-07, Vol.2 (7), p.e279-e287
Hauptverfasser: Noguchi, Lisa M, Dr, Richardson, Barbra A, Prof, Baeten, Jared M, Prof, Hillier, Sharon L, Prof, Balkus, Jennifer E, PhD, Chirenje, Z Mike, Prof, Bunge, Katherine, MD, Ramjee, Gita, PhD, Nair, Gonasagrie, MBChB, Palanee-Phillips, Thesla, PhD, Selepe, Pearl, MBChB, van der Straten, Ariane, Prof, Parikh, Urvi M, PhD, Gomez, Kailazarid, MPM, Piper, Jeanna M, MD, Watts, D Heather, MD, Marrazzo, Jeanne M, Prof
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Zusammenfassung:Summary Background Several observational studies have reported that HIV-1 acquisition seems to be higher in women who use depot medroxyprogesterone acetate (DMPA) than in those who do not use hormonal contraception. We aimed to assess whether two injectable progestin-only contraceptives, DMPA and norethisterone enanthate (NET-EN), confer different risks of HIV-1 acquisition. Methods We included data from South African women who used injectable contraception while participating in the VOICE study, a multisite, randomised, placebo-controlled trial that investigated the safety and efficacy of three formulations of tenofovir for prevention of HIV-1 infection in women between Sept 9, 2009, and Aug 13, 2012. Women were assessed monthly for contraceptive use and incident infection. We estimated the difference in incident HIV-1 infection between DMPA and NET-EN users by Cox proportional hazards regression analyses in this prospective cohort. The VOICE trial is registered with ClinicalTrials.gov , NCT00705679. Findings 3141 South African women using injectable contraception were included in the present analysis: 1788 (56·9%) solely used DMPA, 1097 (34·9%) solely used NET-EN, and 256 (8·2%) used both injectable types at different times during follow-up. During 2733·7 person-years of follow-up, 207 incident HIV-1 infections occurred (incidence 7·57 per 100 person-years, 95% CI 6·61–8·68). Risk of HIV-1 acquisition was higher among DMPA users (incidence 8·62 per 100 person-years, 95% CI 7·35–10·11) than among NET-EN users (5·67 per 100 person-years, 4·35–7·38; hazard ratio 1·53, 95% CI 1·12–2·08; p=0·007). This association persisted when adjusted for potential confounding variables (adjusted hazard ratio [aHR] 1·41, 95% CI 1·06–1·89; p=0·02). Among women seropositive for herpes simplex virus type 2 (HSV-2) at enrolment, the aHR was 2·02 (95% CI 1·26–3·24) compared with 1·09 (0·78–1·52) for HSV-2-seronegative women (pinteraction =0·07). Interpretation Although moderate associations in observational analyses should be interpreted with caution, these findings suggest that NET-EN might be an alternative injectable drug with a lower HIV risk than DMPA in high HIV-1 incidence settings where NET-EN is available. Funding National Institutes of Health, Mary Meyer Scholars Fund, and the Ruth Freeman Memorial Fund.
ISSN:2352-3018
2352-3018
DOI:10.1016/S2352-3018(15)00058-2