Abstract

BackgroundHepatitis B virus (HBV) infection is endemic in South Africa however, there is limited data on the degree of liver disease and geographic variation in HIV/HBV coinfected individuals. In this study, we analysed data from the CIPRA-SA ‘Safeguard the household study’ in order to assess baseline HBV characteristics in HIV/HBV co-infection participants prior to antiretroviral therapy (ART) initiation.Methods812 participants from two South African townships Soweto and Masiphumelele were enrolled in a randomized trial of ART (CIPRA-SA). Participants were tested for hepatitis B surface antigen (HBsAg), hepatitis B e antigen (HBeAg), and HBV DNA. FIB-4 scores were calculated at baseline.ResultsForty-eight (5.9%) were HBsAg positive, of whom 28 (58.3%) were HBeAg positive. Of those with HBV, 29.8% had an HBV DNA<2000 IU/ml and ALT<40 IU/ml ; 83.0% had a FIB-4 score <1.45, consistent with absent or minimal liver disease. HBV prevalence was 8.5% in Masiphumelele compared to 3.8% in Soweto (relative risk 2.3; 95% CI: 1.3–4.0). More participants in Masiphumelele had HBeAg-negative disease (58% vs. 12%, p = 0.002) and HBV DNA levels ≤2000 IU/ml, (43% vs. 6% p<0.007).ConclusionOne third of HIV/HBV co-infected subjects had low HBV DNA levels and ALT while the majority had indicators of only mild liver disease. There were substantial regional differences in HBsAg and HbeAg prevalence in HIV/HBV co-infection between two regions in South Africa. This study highlights the absence of severe liver disease and the marked regional differences in HIV/HBV co-infection in South Africa and will inform treatment decisions in these populations.

Highlights

  • HIV and hepatitis B virus (HBV) co-infection is common in subSaharan Africa with Hepatitis B virus (HBV) infection in HIV co-infection ranging from 5–17% in South Africa [1,2]

  • HIV/HBV co-infection is associated with increased incidence of liver disease and, mortality [3,4], when compared to HBV monoinfection

  • Clinical treatment characteristics, which include hepatitis B e antigen (HBeAg), HBV DNA, ALT, and baseline liver fibrosis, are important predictors of HBV disease progression and are criteria for HBV treatment initiation. These laboratory indicators and how they may vary within populations and are not well characterised in HIV/HBV co-infection in African populations

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Summary

Introduction

HIV and hepatitis B virus (HBV) co-infection is common in subSaharan Africa with HBV infection in HIV co-infection ranging from 5–17% in South Africa [1,2]. Clinical treatment characteristics, which include HBeAg, HBV DNA, ALT, and baseline liver fibrosis, are important predictors of HBV disease progression and are criteria for HBV treatment initiation. These laboratory indicators and how they may vary within populations and are not well characterised in HIV/HBV co-infection in African populations. Neither hepatitis B prevalence nor the distribution of its important clinical characteristics (HBeAg, HBV DNA, or liver fibrosis) may be uniform in sub-. Hepatitis B virus (HBV) infection is endemic in South Africa there is limited data on the degree of liver disease and geographic variation in HIV/HBV coinfected individuals. We analysed data from the CIPRA-SA ‘Safeguard the household study’ in order to assess baseline HBV characteristics in HIV/HBV co-infection participants prior to antiretroviral therapy (ART) initiation

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