Impact of hepatitis B virus co‐infection on response to highly active antiretroviral treatment and outcome in HIV‐infected individuals: a nationwide cohort study

• Published in: HIV medicine Vol. 9; no. 5; pp. 300 - 306
• Main Authors: Omland, LH, Weis, N, Skinhøj, P, Laursen, AL, Christensen, PB, Nielsen, HI, Møller, A, Engsig, F, Sørensen, HT, Obel, N
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.05.2008
• Subjects: Adult; AIDS-Related Opportunistic Infections - drug therapy; AIDS-Related Opportunistic Infections - mortality; Antiretroviral Therapy, Highly Active - methods; CD4 Lymphocyte Count; Cohort Studies; Drug Resistance, Viral; Female; HBV; Hepatitis B virus; Hepatitis B, Chronic - drug therapy; Hepatitis B, Chronic - mortality; HIV; HIV Infections - complications; HIV Infections - drug therapy; HIV Infections - mortality; HIV-1; HIV–HBV co‐infection; Human immunodeficiency virus 1; Humans; Liver Diseases - mortality; Liver Diseases - virology; Male; Prospective Studies; Viral Load - methods
• DOI: 10.1111/j.1468-1293.2008.00564.x
• ISSN: 1464-2662

Background The impact of chronic hepatitis B virus (HBV) infection on viral suppression, immune recovery and mortality in HIV‐1 infected patients on highly active antiretroviral treatment (HAART) is a matter of debate. The impact of HBeAg status is unknown. Methods This prospective cohort study included all adult Danish HIV‐1 infected patients who started HAART between 1 January 1995 and 1 December 2006 (3180 patients). Patients were classified as chronic HBV‐infected (6%), HBV‐negative (87%) or HBV‐unknown (7%). HBV‐positive patients were divided into HBeAg‐positive or ‐negative (3.0 vs. 2.6%). Study endpoints were viral load, CD4 cell count and mortality. Results HBV co‐infection had no impact on response to HAART regarding viral suppression or immune recovery. HBV co‐infection was associated with several outcomes: overall mortality [mortality rate ratio (MRR) 1.5; 95% confidence interval (CI) 1.1–2.1], liver‐related mortality (MRR 4.0; 95% CI 1.6–9.9) and AIDS‐related deaths (MRR 1.7; 95% CI 1.0–3.0). The presence of HBeAg did not influence patients' response to HAART. Conclusions In HIV patients, chronic HBV infection has no impact on response to HAART concerning viral load and increase in CD4 cell count. However, co‐infected patients have an increased mortality compared to HIV‐monoinfected patients.