The Effect of Sexual and Gender Minority Violence on Depression, Hazardous Drinking, Condom Use, and HIV Acquisition: An Individual Participant Data Meta-Analysis of the CohMSM, HPTN 075, and Anza Mapema Cohort Studies in Africa
- PMID: 40498238
- PMCID: PMC12237430
- DOI: 10.1007/s10461-025-04799-4
The Effect of Sexual and Gender Minority Violence on Depression, Hazardous Drinking, Condom Use, and HIV Acquisition: An Individual Participant Data Meta-Analysis of the CohMSM, HPTN 075, and Anza Mapema Cohort Studies in Africa
Abstract
Some sexual and gender minorities (SGM), including men who have sex with men and transgender women, are disproportionately vulnerable to HIV. Many SGM in Africa report experiencing verbal or physical violence due to their sexual and/or gender identities or behaviours. The pathways linking such SGM violence to HIV acquisition are complex. We described experiences of verbal and physical SGM violence and explored pathways to HIV acquisition among SGM assigned male sex at birth using a two-stage individual participant data meta-analysis of three African cohort studies: CohMSM (Burkina Faso, Côte d'Ivoire, Mali, Togo), HPTN 075 (Kenya, Malawi, South Africa), and Anza Mapema (Kenya). SGM violence was assessed at baseline and follow-up visits. We fit log-linear sequential conditional mean models using generalised estimating equations to estimate risk ratios linking SGM violence, moderate-to-severe depressive symptoms, hazardous drinking, condom use, and HIV acquisition, adjusted for baseline confounders and previous exposure and outcome. We pooled study estimates using random effects meta-analysis. SGM violence, mostly verbal, was reported by 36% (570/1590) participants at baseline (past 6-12 months), and 20% (321/1590) during the first year of follow-up (past 3-6 months). Baseline SGM violence was not associated with HIV acquisition (pooled adjusted risk ratio [aRR] = 1.0, 95% CI 0.5-1.9). During follow-up, SGM violence also showed no clear relationship with HIV, but was linked to depressive symptoms at the same visit (pooled aRR = 1.7, 1.3-2.1), in turn associated with hazardous drinking (pooled aRR = 1.4, 1.1-1.7). Impacts on condom use were inconclusive. SGM in Africa face high rates of violence, which are associated with depressive symptoms and hazardous drinking-potential routes to HIV vulnerability. While our study did not conclusively demonstrate higher HIV incidence among SGM reporting violence, interventions to reduce violence and support mental health remain crucial.
Keywords: HIV incidence; Homophobic violence; Individual participant data meta-analysis; Mental health; Sexual and gender minorities; Structural determinants.
© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Conflict of interest: All authors declare no relevant conflicts of interest. Ethical approval: This study is a secondary analysis of three cohorts. In all cohorts, participants provided informed consent to participate. In CohMSM and Anza Mapema, participants provided written consent. In HPTN 075, written consent was provided at three sites, and verbal consent at one site to avoid documentation of study participation that could lead to unintended disclosure. Ethics approval for CohMSM was obtained from the National Ethics Committees of Mali (N°2015/32/CE/FMPOS), Burkina Faso (N°2015-3-037), Côte d’Ivoire (N°021/MSLS/CNER-dkn) and Togo (N°008/2016/MSPSCAB/SG/DPML/ CBRS). Ethics approval for HPTN 075 was provided by Kenya Medical Research Institute (KEMRI; #2994; Nairobi, Kenya); College of Medicine Research Ethics Committee (COMREC; 07/15/1762; Blantyre, Malawi) and Institutional Review Board, Johns Hopkins University School of Public Health (00006252; Baltimore, USA); Human Research Ethics Committee, University of Cape Town, Faculty of Health Sciences (#795/2014; Cape Town, South Africa); Research Ethics Committee (Medical), University of the Witwatersrand Human (Wits HREC Medical; #141105; Johannesburg, South Africa). Additional approval for HPTN 075 was received from the Institutional Review Board, New York State Psychiatric Institute (#6868; New York, USA). Anza Mapema was approved by the Maseno University Ethics Review Committee (MsU/DrPc/MUerc/00104/14), the Institutional Review Board of the University of Illinois at Chicago (2014–0778), and the Human Subjects Division of the University of Washington (48148). All analyses were performed on de-identified data. Ethics approval for this secondary data analysis was obtained from McGill University’s Faculty of Medicine Institutional Review Board (A02-B19-21 A).
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