Hepatitis B virus infection among men who have sex with men and transgender women living with or at risk for HIV: a cross sectional study in Abuja and Lagos, Nigeria
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Published:2021-07-06
Issue:1
Volume:21
Page:
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ISSN:1471-2334
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Container-title:BMC Infectious Diseases
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language:en
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Short-container-title:BMC Infect Dis
Author:
Adeyemi Olusegun A., Mitchell Andrew, Shutt Ashley, Crowell Trevor A., Ndembi Nicaise, Kokogho Afoke, Ramadhani Habib O., Robb Merlin L., Baral Stefan D., Ake Julie A., Charurat Manhattan E., Peel Sheila, Nowak Rebecca G.ORCID, Charurat Manhattan, Ake Julie, Abayomi Aka, Adebajo Sylvia, Baral Stefan, Crowell Trevor, Eluwa George, Gaydos Charlotte, Kokogho Afoke, Malia Jennifer, Makanjuela Olumide, Michael Nelson, Ndembi Nicaise, Nowak Rebecca, Olawore Oluwasolape, Parker Zahra, Peel Sheila, Ramadhani Habib, Robb Merlin, Rodriguez-Hart Cristina, Sanders-Buell Eric, Tovanabutra Sodsai, Vasan Sandhya,
Abstract
Abstract
Background
Despite the development of a safe and efficacious hepatitis B vaccine in 1982, the hepatitis B virus (HBV) remains a public health burden in sub-Saharan Africa. Due to shared risk factors for virus acquisition, men who have sex with men (MSM) and transgender women (TGW) living with HIV are at increased risk of HBV. We estimated the prevalence of HBV and associated factors for MSM and TGW living with or without HIV in Nigeria.
Methods
Since March 2013, TRUST/RV368 has recruited MSM and TGW in Abuja and Lagos, Nigeria using respondent driven sampling. Participants with HIV diagnosis, enrollment as of June 2015, and available plasma were selected for a cross-sectional study and retrospectively tested for hepatitis B surface antigen and HBV DNA. Logistic regression models were used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for factors associated with prevalent HBV infection.
Results
A total of 717 MSM and TGW had a median age of 25 years (interquartile range [IQR]: 21–27), 5% self-reported HBV vaccination, 61% were living with HIV, 10% had prevalent HBV infection and 6% were HIV-HBV co-infected. HIV mono-infected as compared to HIV-HBV co-infected had a higher median CD4 T cell count [425 (IQR: 284–541) vs. 345 (IQR: 164–363) cells/mm3, p = 0.03] and a lower median HIV RNA viral load [4.2 (IQR: 2.3–4.9) vs. 4.7 (IQR: 3.9–5.4) log10copies/mL, p < 0.01]. The only factor independently associated with HBV was self-report of condomless sex at last anal intercourse (OR: 2.2, 95% CI: 1.3, 3.6). HIV infection was not independently associated with HBV (OR: 1.0, 95% CI: 0.7–1.6).
Conclusion
HBV prevalence was moderately high but did not differ by HIV in this cohort of MSM and TGW. Recent condomless sex was associated with elevated HBV risk, reinforcing the need to increase communication and education on condom use among key populations in Nigeria. Evaluating use of concurrent HIV antiretroviral therapy with anti-HBV activity may confirm the attenuated HBV prevalence for those living with HIV.
Funder
National Institute of Allergy and Infectious Diseases National Institute of Mental Health National Cancer Institute Henry M. Jackson Foundation Fogarty International Center U.S. President’s Emergency Plan for AIDS Relief
Publisher
Springer Science and Business Media LLC
Subject
Infectious Diseases
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