Hepatitis B or hepatitis C virus infection is a risk factor for severe hepatic cytolysis after initiation of a protease inhibitor-containing antiretroviral regimen in human immunodeficiency virus-infected patients. The APROCO Study Group

Antimicrob Agents Chemother. 2000 Dec;44(12):3451-5. doi: 10.1128/AAC.44.12.3451-3455.2000.

Abstract

In a cohort of 1,047 human immunodeficiency virus type 1-infected patients started on protease inhibitors (PIs), the incidence of severe hepatic cytolysis (alanine aminotransferase concentration five times or more above the upper limit of the normal level >/= 5N) was 5% patient-years after a mean follow-up of 5 months. Only positivity for hepatitis C virus antibodies (hazard ratio [HR], 7. 95; P < 10(-3)) or hepatitis B virus surface antigen (HR, 6.67; P < 10(-3)) was associated with severe cytolysis. Before starting patients on PIs, assessment of liver enzyme levels and viral coinfections is necessary.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIDS-Related Opportunistic Infections / immunology
  • AIDS-Related Opportunistic Infections / pathology*
  • Adult
  • Alanine Transaminase / metabolism
  • Female
  • HIV Infections / complications
  • HIV Infections / drug therapy*
  • HIV Infections / immunology
  • HIV Infections / pathology
  • HIV Protease Inhibitors / adverse effects
  • HIV Protease Inhibitors / therapeutic use*
  • HIV-1 / immunology
  • Hepacivirus / immunology
  • Hepatitis B / etiology
  • Hepatitis B / immunology
  • Hepatitis B / pathology*
  • Hepatitis B / virology
  • Hepatitis B virus / immunology
  • Hepatitis C / etiology
  • Hepatitis C / immunology
  • Hepatitis C / pathology*
  • Hepatitis C / virology
  • Hepatocytes / drug effects
  • Hepatocytes / pathology*
  • Hepatocytes / virology
  • Humans
  • Liver / pathology*
  • Male
  • Risk Factors

Substances

  • HIV Protease Inhibitors
  • Alanine Transaminase