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   Hormonal Contraception and the Risk of HIV Acquisition: An Individual Participant Data Meta-analysis  
   
نویسنده morrison c.s. ,chen p.-l. ,kwok c. ,baeten j.m. ,brown j. ,crook a.m. ,van damme l. ,delany-moretlwe s. ,francis s.c. ,friedland b.a. ,hayes r.j. ,heffron r. ,kapiga s. ,karim q.a. ,karpoff s. ,kaul r. ,mcclelland r.s. ,mccormack s. ,mcgrath n. ,myer l. ,rees h. ,van der straten a. ,watson-jones d. ,van de wijgert j.h.h.m. ,stalter r. ,low n.
منبع plos medicine - 2015 - دوره : 12 - شماره : 1 - صفحه:1 -26
چکیده    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.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.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. © 2015 morrison et al.
آدرس clinical sciences,fhi 360,durham,nc, United States, biostatistics,fhi 360,durham,nc, United States, biostatistics,fhi 360,durham,nc, United States, department of global health,medicine,and epidemiology,university of washington,seattle,wa, United States, department of epidemiology,university of california,los angeles,los angeles,ca, United States, medical research council,comprehensive clinical trials unit at ucl,university college london,london, United Kingdom, department of global health,bill & melinda gates foundation,seattle,wa, United States, wits reproductive health and hiv institute,johannesburg, South Africa, department of infectious disease epidemiology,london school of hygiene & tropical medicine,london, United Kingdom, population council,new yorkny, United States, department of infectious disease epidemiology,london school of hygiene & tropical medicine,london, United Kingdom, department of global health,medicine,and epidemiology,university of washington,seattle,wa, United States, department of infectious disease epidemiology,london school of hygiene & tropical medicine,london, United Kingdom, center for the aids program of research in south africa,university of kwa-zulu natal,durban, South Africa, diversity research programs,multicenter protocols group,memorial sloan-kettering cancer center,new yorkny, United States, department of medicine,university of toronto,torontoon, Canada, department of global health,medicine,and epidemiology,university of washington,seattle,wa, United States, department of epidemiology,university of california,los angeles,los angeles,ca, United States, department of social statistics and demography,academic unit of primary care,population sciences,university of southampton,southampton, United Kingdom, division of epidemiology and biostatistics,school of public health and family medicine,university of cape town,cape town, South Africa, wits reproductive health and hiv institute,johannesburg, South Africa, women’s global health imperative,rti international,san francisco,ca, United States, department of clinical research,london school of hygiene & tropical medicine,london, United Kingdom, department of clinical infection,microbiology and immunology,institute of infection and global health,university of liverpool,merseyside, United Kingdom, clinical sciences,fhi 360,durham,nc, United States, institute of social and preventive medicine,university of bern,bern, Switzerland
 
     
   
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