PNPLA3 rs738409 polymorphism is associated with liver fibrosis progression in patients with chronic hepatitis C: A repeated measures study

J Clin Virol. 2018 Jun:103:71-74. doi: 10.1016/j.jcv.2018.04.008. Epub 2018 Apr 12.

Abstract

Background: Host genetic background has been associated with liver fibrosis progression.

Objective: To analyze the association between the patatin-like phospholipase domain-containing 3 (PNPLA3) rs738409 polymorphism and liver fibrosis progression in hepatitis C virus (HCV)-infected patients.

Study design: In this retrospective cohort study, 187 patients with chronic HCV infection were included, who had at least two liver stiffness measurements (LSM) by transient elastography during the follow-up. Results were expressed in kilopascals (kPa). The analysis of genetic association was carried out according to additive model by using Generalized Linear Models.

Results: No patients had advanced fibrosis/cirrhosis at baseline. During a median follow-up time of 47.9 months, 15 patients developed advanced fibrosis and 17 cirrhosis. In multivariate analysis adjusted by the main clinical and epidemiological covariates, the rs738409 G allele was related to higher increase of LSM values during the follow-up (adjusted arithmetic mean ratio (aAMR) = 1.16 (95%CI = 1.04; 1.29); p = .006) and higher odds of having progression to advanced fibrosis [aOR = 2.03 (95%CI = 1.01; 4.06); p = .045], and progression to cirrhosis [aOR = 3.03 (95%CI = 1.26; 7.30); p = .014].

Conclusions: PNPLA3 rs738409 polymorphism appears to be related to the increased progression of liver fibrosis in HCV infected patients.

Keywords: Chronic hepatitis C; Cirrhosis; Hepatic fibrosis; Liver stiffness; PNPLA3; SNPs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Disease Progression
  • Disease Susceptibility*
  • Elasticity Imaging Techniques
  • Female
  • Genetic Association Studies
  • Hepatitis C, Chronic / complications*
  • Humans
  • Lipase / genetics*
  • Liver / pathology
  • Liver Cirrhosis / genetics*
  • Longitudinal Studies
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Retrospective Studies

Substances

  • Membrane Proteins
  • Lipase
  • adiponutrin, human