Association between liver fibrosis and insulin sensitivity in chronic hepatitis C patients

Am J Gastroenterol. 2006 Dec;101(12):2752-9. doi: 10.1111/j.1572-0241.2006.00835.x. Epub 2006 Oct 6.

Abstract

Background: Several clinical studies have suggested a possible link between chronic hepatitis caused by hepatitis C virus (HCV) and the development of diabetes mellitus. We investigated the association between liver fibrosis and glucose intolerance in HCV-infected patients by measuring insulin sensitivity and beta-cell function.

Method: A total of 83 chronic HCV-infected patients were recruited into this study. We evaluated insulin sensitivity and beta-cell function of all patients in a fasting state (homeostasis model assessment of insulin resistance [HOMA-R] and homeostasis model assessment of beta-cell function [HOMA-beta]) and after an oral load of 75 g glucose (whole-body insulin sensitivity index [WBISI] and Delta-insulin/Delta-glucose 30).

Results: In a multivariate analysis, severe fibrosis was the only independent factor associated with insulin resistance. There were significant differences in both HOMA-R (P= 0.0063) and WBISI (P= 0.0159) between patients with mild fibrosis (N = 34) and those with severe fibrosis (N = 49). Although HOMA-beta was increased significantly in the subjects with severe fibrosis compared with those with mild fibrosis (P= 0.0169), Delta-insulin/Delta-glucose 30 showed no significant difference in stage of liver fibrosis, suggesting an uncertain association between liver fibrosis and beta-cell function.

Conclusion: Our findings suggest that the development of liver fibrosis is associated with insulin resistance in HCV-infected patients.

MeSH terms

  • Blood Glucose / metabolism
  • Case-Control Studies
  • Female
  • Glucose Tolerance Test
  • Hepatitis C, Chronic / blood*
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / physiopathology*
  • Humans
  • Insulin / blood
  • Insulin Resistance / physiology*
  • Insulin-Secreting Cells / physiology
  • Liver Cirrhosis / blood*
  • Liver Cirrhosis / physiopathology*
  • Liver Cirrhosis / virology
  • Male
  • Middle Aged

Substances

  • Blood Glucose
  • Insulin