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Hepatitis B and C virus coinfection in The TREAT Asia HIV Observational Database
Author(s) -
Zhou Jialun,
Dore Gregory J,
Zhang Fujie,
Lim Poh Lian,
Chen YiMing A
Publication year - 2007
Publication title -
journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.214
H-Index - 130
eISSN - 1440-1746
pISSN - 0815-9319
DOI - 10.1111/j.1440-1746.2007.05062.x
Subject(s) - medicine , coinfection , hbsag , hazard ratio , hepatitis b virus , hepatitis c virus , hepatitis b , hepatitis c , viral load , confidence interval , virology , immunology , virus
Background and Aim: Most studies of hepatitis B virus (HBV) and hepatitis C virus (HCV) coinfection with HIV have been conducted among Western patient populations. This study aims to assess rates of HBV and HCV coinfection, and their impact on response to antiretroviral therapy and mortality, using data from The TREAT Asia HIV Observational Database (TAHOD), a multi‐center cohort of patients with HIV in the Asia–Pacific region. Methods: Patients who had been tested either HBV surface antigen (HBsAg) or HCV antibody were included. Patients who ever tested positive for HBV or HCV were regarded as coinfected for the duration of the study. Results: Results of hepatitis tests were available for 55% (HBV) and 49% (HCV) of 2979 TAHOD patients, with prevalence of HBV and HCV coinfection both at approximately 10%. Mean CD4 change at 180 days after antiretroviral treatment initiation was 118.8 cells/μL and patients with either HBV or HCV had a lower but non‐significant CD4 increase compared with patients with HIV only. Median time to reach undetectable viral load (<400 copies/mL) was 148 days and was not independently associated with HBV or HCV. In univariate analysis, patients with HCV had increased mortality (unadjusted hazard ratio, HR 2.80, P = 0.007). However, neither HBV (adjusted HR 0.80, 95% confidence interval CI 0.24–2.64, P = 0.710) nor HCV (adjusted HR 1.06, 95% CI 0.40–2.79, P = 0.905) was associated with increased mortality after adjustment for other covariates. Both HBV and HCV remained independently associated with elevated alanine aminotransferase (ALT) in the multivariate model (HBV, adjusted HR 1.94, 95% CI 1.04–3.62, P = 0.037; HCV, adjusted HR 2.74, 95% CI 1.47–5.12, P = 0.002). Conclusion: The impact of hepatitis coinfection on immunological and virological responses to antiretroviral therapy and HIV disease progression among this Asian cohort are similar to that seen in Western countries. The longer‐term impact of hepatitis coinfection on both HIV disease and liver disease morbidity and mortality needs to be monitored.