Genetic variants in PNPLA3 and risk of non-alcoholic fatty liver disease in a Han Chinese population

PLoS One. 2012;7(11):e50256. doi: 10.1371/journal.pone.0050256. Epub 2012 Nov 30.

Abstract

We investigated the possible association between genetic variants in the Patatin like phospholipase-3 (PNPLA3) gene and nonalcoholic fatty liver disease (NAFLD) in a Han Chinese population. We evaluated twelve tagging single-nucleotide polymorphisms (tSNPs) of the PNPLA3 gene in a frequency matched case-control study from Fuzhou city of China (553 cases, 553 controls). In the multivariate logistic regression analysis, the rs738409 GG or GC, and rs139051 TT genotypes were found to be associated with increased risk of NAFLD, and a significant trend of increased risk with increasing numbers of risk genotype was observed in the cumulative effect analysis of these single nucleotide polymorphisms. Furthermore, haplotype association analysis showed that, compared with the most common haplotype, the CAAGAATGCGTG and CGAAGGTGTCCG haplotypes conferred a statistically significant increased risk for NAFLD, while the CGGGAACCCGCG haplotype decreased the risk of NAFLD. Moreover, rs738409 C>G appeared to have a multiplicative joint effect with tea drinking (P<0.005) and an additive joint effect with obesity (Interaction contrast ratio (ICR) = 2.31, 95% CI: 0.7-8.86), hypertriglyceridemia (ICR = 3.07, 95% CI: 0.98-5.09) or hypertension (ICR = 1.74, 95% CI: 0.52-3.12). Our data suggests that PNPLA3 genetic polymorphisms might influence the susceptibility to NAFLD development independently or jointly in Han Chinese.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Asian People*
  • Case-Control Studies
  • Fatty Liver / complications
  • Fatty Liver / enzymology
  • Fatty Liver / ethnology
  • Fatty Liver / genetics*
  • Female
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Hypertension / complications
  • Hypertension / enzymology
  • Hypertension / ethnology
  • Hypertension / genetics
  • Hypertriglyceridemia / complications
  • Hypertriglyceridemia / enzymology
  • Hypertriglyceridemia / ethnology
  • Hypertriglyceridemia / genetics
  • Lipase / genetics*
  • Lipase / metabolism
  • Liver / enzymology*
  • Liver / pathology
  • Male
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease
  • Obesity / complications
  • Obesity / enzymology
  • Obesity / ethnology
  • Obesity / genetics
  • Polymorphism, Single Nucleotide*
  • Risk
  • Tea

Substances

  • Membrane Proteins
  • Tea
  • Lipase
  • adiponutrin, human

Grants and funding

This work was supported by grants from the National Natural Science Foundation of China (No. 81001279), Fujian Science and Technology Innovation Foundation for Young Scientists (No. 2010J05067), the Science Foundation for Distinguished Young Scholars of Fujian province (No. 2009J06016), the Key Program of Scientific Research of Fujian Medical University (09ZD004), and the Foundation of Fujian Educational Committee (No. JA10138 and No.JK2009014). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.