R Matthew Chico1, Motoyuki Tsuboi2, Jayne Evans2, Ella P Davies2, Jane Rowley3, Eline L Korenromp4, Tim Clayton5, David Mabey6, Melanie M Taylor7. 1. Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK. Electronic address: matthew.chico@lshtm.ac.uk. 2. Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK. 3. London, United Kingdom. 4. Avenir Health, Geneva, Switzerland. 5. Faculty of Infectious and Tropical Diseases, and Department of Medical Statistics, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK. 6. Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK. 7. Centers for Disease Control and Prevention, Division of STD Prevention, Atlanta, GA, USA.
Can a change in venues sampled in syphilis serosurveys influence prevalence
estimates among men who have sex with men (MSM), and has this contributed to
spurious trends of decline in the past decade? In this issue of The Lancet
Global Health, Ting-Ting Jiang and colleagues in their Correspondence
pose this question and note evidence from China that HIV prevalence evaluated among
MSM at public bathhouses and saunas is consistently higher than among MSM recruited
through internet sites.[1] This
difference in testing venues could extend to syphilis, although such a difference
was not apparent in our recent global systematic review and meta-analysis of
syphilis prevalence among MSM published in The Lancet Global
Health.[2] In our
study, the pooled prevalence estimate of syphilis among studies that recruited MSM
at venues including bathhouses and saunas, clubs, and one-off public events was
6·1% (95% CI 3·7–9·1; 13 229 MSM; 29 data points). When
taking into account MSM studies that used a variety of convenience sampling methods,
including internet advertising, the pooled prevalence estimate was 8·7% (95%
CI 7·6–9·9%; 109 065 MSM; 64 data points). Neither of these
subgroup estimates were meaningfully different from our overall pooled estimate of
7·5% (95% CI 7·0–8·0; 606 232 MSM; 345 data points).
However, a prevalence data compilation and trend estimation of syphilis in Yunnan
province, China did find prevalence among MSM (or female sex workers) to be
systematically lower in routine annual surveillance surveys and higher in research
studies.[3] The venues
involved might have contributed to this difference, although neither dataset (nor
their weighted sum) showed a statistically significant upward or downward prevalence
trend over 2010–17; these findings do highlight the importance of inferring
time trends only within series of methodologically comparable samples.There is a need to continue harmonising prevalence-data collection and
reporting of syphilis and other sexually transmitted infections (STI) among MSM.
Syphilis prevalence might vary by venue and over time, the interactions of which
might be best quantified and adjusted if common methods and protocols are used for
screening and evaluation. These adjustments can take the form of adapting elements
from the survey protocol published by WHO to test for gonorrhoea and chlamydia among
pregnant women in antenatal care clinics,[4] as Jiang and colleagues suggest. Countries and national HIV
and STI programmes are encouraged to continue screening for active syphilis among
MSM (and female sex workers) and reporting data through the UNAIDS Global AIDS
Monitoring system. Notably, we used syphilis prevalence data from 67 Integrated
Bio-Behavioural Surveillance surveys provided by UNAIDS in our
meta-analysis.[2] Efforts to
harmonise data collection and reporting is as important now as ever with the aim of
reducing worldwide syphilis incidence by 90% between 2018 and 2030, as proposed in
the WHO’s Global Health Sector Strategy for STI control.[5]
Authors: Motoyuki Tsuboi; Jayne Evans; Ella P Davies; Jane Rowley; Eline L Korenromp; Tim Clayton; Melanie M Taylor; David Mabey; R Matthew Chico Journal: Lancet Glob Health Date: 2021-07-08 Impact factor: 38.927