Hepatic steatosis in HIV-HCV coinfected patients receiving antiretroviral therapy is associated with HCV-related factors but not antiretrovirals

BMC Res Notes. 2012 Jul 9:5:180. doi: 10.1186/1756-0500-5-180.

Abstract

Background: In HIV and hepatitis C virus (HCV) coinfected patients, the role of antiretroviral therapy (ART) on hepatic steatosis (HS) remains controversial.

Methods: HIV/HCV coinfected patients receiving ART and previously untreated for HCV who underwent a liver biopsy were included. Cumulative duration of exposure to each antiretroviral was recorded up to liver biopsy date. Logistic regression analyses evaluated factors associated with steatosis and its severity.

Results: 184 patients were included: median age 41 years, 84% male, 89% Caucasian, 61% with a past history of intravenous drug use. HCV genotypes were 1 (55%), 2 (6%), 3 (26%), and 4 (13%). Median HCV-RNA was 6.18 log10 IU/ml. HIV-RNA was undetectable (<400 copies/ml) in 67% of patients. Median CD4 count was 321/mm3. All patients had been exposed to nucleoside reverse transcriptase inhibitors (median cumulative exposure 56 months); 126 received protease inhibitors (23 months), and 79 non-nucleoside reverse transcriptase inhibitors (16 months). HS was observed in 102 patients (55%): 41% grade 1; 5% grade 2, and 9% grade 3. In multivariate analysis, HCV genotype 3 and HCV viral load were moderately associated with mild steatosis but strongly with grade 2-3 steatosis. After adjustment for the period of biopsy, no association was detected between HS and exposure to any antiretroviral class or drug, or duration of ART globally or comparing genotype 3 to others.

Conclusions: Among our ART-treated HIV-HCV cohort predominantly infected with genotype 1, 55% of patients had HS which was associated with HCV-related factors, but not ART class or duration of exposure.

MeSH terms

  • Adult
  • Anti-Retroviral Agents / therapeutic use
  • Coinfection / complications*
  • Coinfection / drug therapy
  • Coinfection / virology
  • Fatty Liver / complications*
  • Female
  • Genotype
  • HIV Infections / complications*
  • HIV Infections / drug therapy
  • HIV Infections / virology
  • Hepacivirus / genetics
  • Hepacivirus / physiology
  • Hepatitis C / complications*
  • Hepatitis C / drug therapy
  • Hepatitis C / virology
  • Host-Pathogen Interactions
  • Humans
  • Liver / pathology
  • Liver / virology
  • Logistic Models
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Retrospective Studies
  • Reverse Transcriptase Inhibitors / therapeutic use
  • Risk Assessment / methods
  • Risk Factors
  • Severity of Illness Index
  • Viral Load

Substances

  • Anti-Retroviral Agents
  • Reverse Transcriptase Inhibitors