Abstract

BackgroundWe assessed the effects of hepatitis B (HBV) or hepatitis C (HCV) co-infection on outcomes of antiretroviral therapy (ART) in HIV-infected patients enrolled in the TREAT Asia HIV Observational Database (TAHOD), a multi-center cohort of HIV-infected patients in the Asia-Pacific region.MethodsPatients testing HBs antigen (Ag) or HCV antibody (Ab) positive within enrollment into TAHOD were considered HBV or HCV co-infected. Factors associated with HBV and/or HCV co-infection were assessed by logistic regression models. Factors associated with post-ART HIV immunological response (CD4 change after six months) and virological response (HIV RNA <400 copies/ml after 12 months) were also determined. Survival was assessed by the Kaplan-Meier method and log rank test.ResultsA total of 7,455 subjects were recruited by December 2012. Of patients tested, 591/5656 (10.4%) were HBsAg positive, 794/5215 (15.2%) were HCVAb positive, and 88/4966 (1.8%) were positive for both markers. In multivariate analysis, HCV co-infection, age, route of HIV infection, baseline CD4 count, baseline HIV RNA, and HIV-1 subtype were associated with immunological recovery. Age, route of HIV infection, baseline CD4 count, baseline HIV RNA, ART regimen, prior ART and HIV-1 subtype, but not HBV or HCV co-infection, affected HIV RNA suppression. Risk factors affecting mortality included HCV co-infection, age, CDC stage, baseline CD4 count, baseline HIV RNA and prior mono/dual ART. Shortest survival was seen in subjects who were both HBV- and HCV-positive.ConclusionIn this Asian cohort of HIV-infected patients, HCV co-infection, but not HBV co-infection, was associated with lower CD4 cell recovery after ART and increased mortality.

Highlights

  • There are similarities in the transmission routes of and risk factors for HIV, and the hepatitis B virus (HBV) and hepatitis C virus (HCV) infection[1,2], but each has a different biology and natural history of chronic infection

  • With faster liver disease progression in HIV patients with hepatitis B and C, declining risk of AIDS-related opportunistic infections and increased life expectancy seen in HIV-infected patients on antiretroviral therapy (ART), HBV and HCV have emerged as important causes of liver-related morbidity and mortality in these patients.[5,6,7,8,9,10,11,12,13]

  • While HIV virological response to ART does not seem to be affected by HBV or HCV co-infection, the impact of viral hepatitis coinfection on immunological recovery after initiation of ART remains a topic of study.[16,17,18,19,20]

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Summary

Introduction

There are similarities in the transmission routes of and risk factors for HIV, and the hepatitis B virus (HBV) and hepatitis C virus (HCV) infection[1,2], but each has a different biology and natural history of chronic infection. While HIV virological response to ART does not seem to be affected by HBV or HCV co-infection, the impact of viral hepatitis coinfection on immunological recovery after initiation of ART remains a topic of study.[16,17,18,19,20] The aims of our study were to assess the effects of HBV or HCV co-infection on short- and long-term outcomes following ART initiation in patients enrolled in the TREAT Asia HIV Observational Database (TAHOD), a multi-center observational research cohort in the AsiaPacific region. We assessed the effects of hepatitis B (HBV) or hepatitis C (HCV) co-infection on outcomes of antiretroviral therapy (ART) in HIV-infected patients enrolled in the TREAT Asia HIV Observational Database (TAHOD), a multi-center cohort of HIV-infected patients in the Asia-Pacific region

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