Update on nonalcoholic fatty liver disease: genes involved in nonalcoholic fatty liver disease and associated inflammation

Curr Opin Clin Nutr Metab Care. 2010 Jul;13(4):391-6. doi: 10.1097/MCO.0b013e32833a87cc.


Purpose of review: Nonalcoholic fatty liver disease (NAFLD) is one of the most prevalent liver diseases worldwide. Advanced age, extensive overweight and a number of features of the metabolic syndrome are associated with NAFLD severity. The cause of NAFLD is considered multifactorial with a substantial genetic component.

Recent findings: Family members of children with NAFLD demonstrate a higher risk for NAFLD. Whereas such an association only suggests that familial factors are major determinants of whether or not an individual will develop NAFLD, recent genome-wide association studies were able to identify first candidate genes. An allele in patatin-like phospholipase 3, encoding a protein of unknown function with homology to lipid acyl hydrolases, is strongly associated with increased hepatic fat and inflammation. Apolipoprotein C3 gene variants are also associated with NAFLD and insulin resistance. Several other genetic variants have been identified, although with less convincing evidence. These genetic variants involve molecules regulating insulin signaling, lipid metabolism, oxidative stress or fibrogenesis. Furthermore, genetic variants of several cytokines and adipocytokines have been associated with NAFLD.

Summary: Several genetic factors such as patatin-like phospholipase 3 or apolipoprotein C3 have been recently characterized in NAFLD. Further studies to identify their interaction with environmental factors are eagerly warranted.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Apolipoprotein C-III / genetics*
  • Cytokines / genetics
  • Fatty Liver / complications
  • Fatty Liver / genetics*
  • Fibrosis / genetics
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Humans
  • Hydrolases / genetics
  • Inflammation / complications
  • Inflammation / genetics*
  • Insulin / genetics*
  • Insulin Resistance / genetics
  • Lipid Metabolism / genetics
  • Obesity / complications
  • Obesity / genetics*
  • Oxidative Stress / genetics
  • Phospholipases / genetics*


  • Apolipoprotein C-III
  • Cytokines
  • Genetic Markers
  • Insulin
  • Hydrolases
  • Phospholipases