High seroprevalence of HBV and HCV infection in HIV-infected adults in Kigali, Rwanda

PLoS One. 2013 May 22;8(5):e63303. doi: 10.1371/journal.pone.0063303. Print 2013.

Abstract

Background: Data on prevalence and incidence of hepatitis B virus (HBV) and hepatitis C virus (HCV) infection in Rwanda are scarce.

Methods: HBV status was assessed at baseline and Month 12, and anti-HCV antibodies at baseline, in a prospective cohort study of HIV-infected patients in Kigali, Rwanda: 104 men and 114 women initiating antiretroviral therapy (ART) at baseline, and 200 women not yet eligible for ART.

Results: Baseline prevalence of active HBV infection (HBsAg positive), past or occult HBV infection (anti-HBc positive and HBsAg negative) and anti-HCV was 5.2%, 42.9%, and 5.7%, respectively. The active HBV incidence rate was 4.2/1,000 person years (PY). In a multivariable logistic regression model using baseline data, participants with WHO stage 3 or 4 HIV disease were 4.19 times (95% CI 1.21-14.47) more likely to have active HBV infection, and older patients were more likely to have evidence of past exposure to HBV (aRR 1.03 per year; 95%CI 1.01-1.06). Older age was also positively associated with having anti-HCV antibodies (aOR 1.09; 95%CI 1.04-1.14) while having a higher baseline HIV viral load was negatively associated with HCV (aOR 0.60; 95% CI 0.40-0.98). The median CD4 increase during the first 12 months of ART was lower for those with active HBV infection or anti-HCV at baseline. Almost all participants (88%) with active HBV infection who were on ART were receiving lamivudine monotherapy for HBV.

Conclusion: HBV and HCV are common in HIV-infected patients in Rwanda. Regular HBsAg screening is needed to ensure that HIV-HBV co-infected patients receive an HBV-active ART regimen, and the prevalence of occult HBV infection should be determined. Improved access to HBV vaccination is recommended. Active HCV prevalence and incidence should be investigated further to determine whether HCV RNA PCR testing should be introduced in Rwanda.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiretroviral Therapy, Highly Active / methods
  • CD4 Antigens / immunology
  • Cohort Studies
  • Coinfection / epidemiology
  • Coinfection / immunology
  • Coinfection / virology
  • Disease Progression
  • Female
  • HIV
  • HIV Infections / complications
  • HIV Infections / drug therapy
  • HIV Infections / immunology
  • HIV Infections / virology*
  • Hepacivirus / immunology
  • Hepatitis B / epidemiology*
  • Hepatitis B / immunology
  • Hepatitis B / virology*
  • Hepatitis B virus / immunology
  • Hepatitis C / epidemiology*
  • Hepatitis C / immunology
  • Hepatitis C / virology*
  • Hepatitis C Antibodies / immunology
  • Humans
  • Male
  • Prevalence
  • Prospective Studies
  • Rwanda / epidemiology
  • Seroepidemiologic Studies
  • Viral Load / immunology

Substances

  • CD4 Antigens
  • Hepatitis C Antibodies

Grants and funding

This work was part of the INTERACT Program funded by the Netherlands-African Partnership for Capacity Development and Clinical Interventions against Poverty-related Diseases (NACCAP) of the Netherlands Organisation for Scientific Research – The Netherlands Foundation for the Advancement of Tropical Research (NWO/WOTRO; URL: http://www.nwo.nl/nwohome.nsf/pages/NWOP_5VWBMM_Eng). Funding was also received from the European and Developing Countries Clinical Trials Partnership (EDCTP) as part of a project entitled: ‘Preparing for Phase III vaginal microbicide trials in Rwanda and Kenya: Preparedness studies, capacity building, and strengthening of medical referral systems’ (CT_ct_05_33070_001; URL: http://www.edctp.org/). The views expressed in this paper are those of the authors and do not necessarily represent the official position of NWO-WOTRO or EDCTP. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.