Insulin resistance and liver steatosis in chronic hepatitis C infection genotype 3

World J Gastroenterol. 2014 Nov 7;20(41):15233-40. doi: 10.3748/wjg.v20.i41.15233.

Abstract

Hepatitis C virus (HCV) infection is a common chronic liver disease worldwide. Non-alcoholic fatty liver disease and insulin resistance (IR) are the major determinants of fibrosis progression and response to antiviral therapy. The pathogenetic link between IR and chronic HCV infection is complex, and is associated with HCV genotype. Liver steatosis is the most common in the patients infected with genotype 3 virus, possibly due to direct effects of genotype 3 viral proteins. To the contrary, hepatic steatosis in the patients infected with other genotypes is thought to be mostly due to the changes in host metabolism, involving IR. In HCV genotype 3, liver steatosis correlates with viral load, reverts after reaching the sustained virologic response and reoccurs in the relapsers. A therapeutic strategy to improve IR and liver steatosis and subsequently the response to antiviral treatment in these patients is warranted.

Keywords: Genotype 3; Hepatitis C virus; Insulin resistance; Non-alcoholic fatty liver disease; Sustained virological response.

Publication types

  • Review

MeSH terms

  • Antiviral Agents / therapeutic use
  • Blood Glucose / metabolism
  • Genotype
  • Hepacivirus / genetics
  • Hepacivirus / pathogenicity*
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / diagnosis
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / virology*
  • Host-Pathogen Interactions
  • Humans
  • Insulin / blood
  • Insulin Resistance*
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Liver / virology*
  • Non-alcoholic Fatty Liver Disease / blood
  • Non-alcoholic Fatty Liver Disease / diagnosis
  • Non-alcoholic Fatty Liver Disease / drug therapy
  • Non-alcoholic Fatty Liver Disease / virology*
  • Prognosis
  • Risk Factors
  • Signal Transduction

Substances

  • Antiviral Agents
  • Blood Glucose
  • Insulin