Prevalence of curable sexually transmitted infections (STIs)– chlamydia, gonorrhoea, syphilis and trichomoniasis – among women aged 15 to 24 exceeds that of older women and similar-aged men in sub-Saharan Africa, according to research.
In one study, Elizabeth A Torrone of the US Centres for Disease Control and Prevention and colleagues performed a meta-analysis of individual participant data from 18 prior studies of HIV prevention.
In the other, Suzanna C Francis of the London School of Hygiene & Tropical Medicine and colleagues obtained new data within the structure of an established health surveillance project. The studies examine STI prevalence within age, sex, setting, and risk groups and further establish young women’s sexual health as a priority issue in the region.
STIs are often asymptomatic, but can have devastating consequences including infertility and pelvic inflammatory disease. They can also increase the risk of HIV infection. Better information on STI prevalence is difficult to collect, particularly in sub-Saharan Africa, where inexpensive, feasible diagnostic tests are not available in most clinical settings.
To address this gap with available data, Torrone and colleagues conducted a meta-analysis using STI test results from 18 HIV prevention studies conducted in Eastern and Southern Africa between 1993 and 2011. In these studies, a total of more than 37,000 HIV-negative women were tested at baseline for curable STIs, the chronic, treatable STI herpes simplex virus type 2 (HSV-2), and the dysbiotic condition bacterial vaginosis (BV) to estimate the prevalence of STIs and BV by age, region and population-type.
Meanwhile, Francis and colleagues tested a pragmatic approach for collection of new data, by conducting nested STI surveillance within the Africa Health Research Institute (AHRI), a health and demographic surveillance site (HDSS) in rural KwaZulu-Natal, South Africa. Between October 2016 and January 2017, the researchers conducted home visits offering testing for STIs and BV to young people who were found at home and agreed to participate.
The studies estimated that, in most groups, more than 10% of young, female participants (aged 15-24) were infected with one or more curable STI. Torrone et al report that estimated prevalence of curable STIs was generally higher in women aged 15-24 than in women aged 25-49. Both studies estimate higher prevalence of HSV-2 and BV, compared with curable STI, in most groups; – Torrone et al estimate HSV-2 prevalence of 39% [95% CI: 34.3%, 44.6%] and BV prevalence of 42.1% [35.6%, 49.0%] among women aged 15-24 in South African clinic and community-based populations.
Francis et al also provide some of the first population data for STI burden in young men (chlamydia: 5% of men, 11% of women; HSV-2: 17% of men, 29% of women; BV: 42% of women). In Francis’ et al’s study, most (75%) of the curable STIs in women were asymptomatic.
The study heterogeneity observed in Torrone et al’s meta-analysis, and the non–population-based sampling, underscore the need to strengthen surveillance efforts. The prevalence estimates gathered by Francis et al are also not fully representative; notably, successful contact with male and migrant individuals was low. However, the two studies provide broadly consistent findings, and demonstrate means of using existing data and established systems to obtain STI/BV prevalence estimates where routine surveillance is limited.
Background: Estimates of sexually transmitted infection (STI) prevalence are essential for efforts to prevent and control STIs. Few large STI prevalence studies exist, especially for low- and middle-income countries (LMICs). Our primary objective was to estimate the prevalence of chlamydia, gonorrhea, trichomoniasis, syphilis, herpes simplex virus type 2 (HSV-2), and bacterial vaginosis (BV) among women in sub-Saharan Africa by age, region, and population type.
Methods and findings: We analyzed individual-level data from 18 HIV prevention studies (cohort studies and randomized controlled trials; conducted during 1993–2011), representing >37,000 women, that tested participants for ≥1 selected STIs or BV at baseline. We used a 2-stage meta-analysis to combine data. After calculating the proportion of participants with each infection and standard error by study, we used a random-effects model to obtain a summary mean prevalence of each infection and 95% confidence interval (CI) across ages, regions, and population types. Despite substantial study heterogeneity for some STIs/populations, several patterns emerged. Across the three primary region/population groups (South Africa community-based, Southern/Eastern Africa community-based, and Eastern Africa higher-risk), prevalence was higher among 15–24-year-old than 25–49-year-old women for all STIs except HSV-2. In general, higher-risk populations had greater prevalence of gonorrhea and syphilis than clinic/community-based populations. For chlamydia, prevalence among 15–24-year-olds was 10.3% (95% CI: 7.4%, 14.1%; I2 = 75.7%) among women specifically recruited from higher-risk settings for HIV in Eastern Africa and was 15.1% (95% CI: 12.7%, 17.8%; I2 = 82.3%) in South African clinic/community-based populations. Among clinic/community-based populations, prevalence was generally greater in South Africa than in Southern/Eastern Africa for most STIs; for gonorrhea, prevalence among 15–24-year-olds was 4.6% (95% CI: 3.3%, 6.4%; I2 = 82.8%) in South Africa and was 1.7% (95% CI: 1.2%, 2.6%; I2 = 55.2%) in Southern/Eastern Africa. Across the three primary region/population groups, HSV-2 and BV prevalence was high among 25–49-year-olds (ranging from 70% to 83% and 33% to 44%, respectively). The main study limitation is that the data are not from random samples of the target populations.
Conclusions: Combining data from 18 HIV prevention studies, our findings highlight important features of STI/BV epidemiology among sub-Saharan African women. This methodology can be used where routine STI surveillance is limited and offers a new approach to obtaining critical information on STI and BV prevalence in LMICs.
Torrone EA, Morrison CS, Chen P-L, Kwok C, Francis SC, Hayes RJ, Looker KJ, McCormack S, McGrath N, van de Wijgert JHHM, Watson-Jones D, Low N, Gottlieb SL on behalf of the STIMA working group