IL28B polymorphism is associated with fatty change in the liver of chronic hepatitis C patients

J Gastroenterol. 2012 Jul;47(7):834-44. doi: 10.1007/s00535-012-0550-y. Epub 2012 Feb 18.

Abstract

Background: Several single nucleotide polymorphisms (SNPs) within the interleukin 28B (IL28B) locus are associated with sustained viral response in chronic hepatitis C (HCV) patients who were treated with pegylated interferon (PEG-IFN) plus ribavirin (RBV) combination therapy. Recently, an association between γ-GTP level and IL28B genotype was identified. In this study, the relationship between IL28B genotype and liver steatosis was analyzed.

Methods: One hundred fifty-three patients who underwent liver biopsy before PEG-IFN plus RBV combination therapy were enrolled. The level of liver steatosis was measured using a BIOREVO BZ-9000 microscope, and the proportion of fatty change and clear cell change were calculated using Dynamic cell count BZ-H1C software. IL28B SNP genotype (rs8099917) was determined using the Invader Assay.

Results: Vesicular change was significantly associated with body mass index (BMI), HCV RNA titer, serum aspartate aminotransferase, γ-GTP, IL28B genotype and liver fibrosis level (P < 0.05). Clear cell change was significantly associated with serum aspartate aminotransferase, γ-GTP and IL28B genotype by univariate logistic regression analysis (P < 0.05). Under multiple logistic regression, IL28B genotype (OR(adj) = 8.158; 95% CI 2.412-27.589), liver fibrosis (OR(adj) = 2.541; 95% CI 1.040-6.207) and BMI (OR(adj) = 1.147; 95% CI 1.011-1.301) were significant independent factors for vesicular change and IL28B genotype (OR(adj) = 3.000; 95% CI 1.282-7.019) for clear cell change.

Conclusion: In this study, a new quantitative method to objectively evaluate hepatic steatosis was described. IL28B genotypes were significantly associated with both vesicular and clear cell changes of livers in chronic hepatitis C patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / therapeutic use*
  • Fatty Liver / genetics*
  • Fatty Liver / pathology
  • Female
  • Genotype
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / genetics*
  • Hepatitis C, Chronic / pathology
  • Humans
  • Interferons / administration & dosage
  • Interferons / therapeutic use
  • Interleukins / genetics*
  • Liver / pathology
  • Logistic Models
  • Male
  • Middle Aged
  • Polyethylene Glycols / chemistry
  • Polymorphism, Single Nucleotide
  • Ribavirin / administration & dosage
  • Ribavirin / therapeutic use
  • Young Adult

Substances

  • Antiviral Agents
  • interferon-lambda, human
  • Interleukins
  • Polyethylene Glycols
  • Ribavirin
  • Interferons