Review: The role of insulin resistance in nonalcoholic fatty liver disease

J Clin Endocrinol Metab. 2006 Dec;91(12):4753-61. doi: 10.1210/jc.2006-0587. Epub 2006 Sep 12.

Abstract

Context: Insulin resistance is an almost universal finding in nonalcoholic fatty liver disease (NAFLD). This review outlines the evidence linking insulin resistance and NAFLD, explores whether liver fat is a cause or consequence of insulin resistance, and reviews the current evidence for treatment of NAFLD.

Evidence acquisition: Evidence from epidemiological, experimental, and clinical research studies investigating NAFLD and insulin resistance was reviewed.

Evidence synthesis: Insulin resistance in NAFLD is characterized by reductions in whole-body, hepatic, and adipose tissue insulin sensitivity. The mechanisms underlying the accumulation of fat in the liver may include excess dietary fat, increased delivery of free fatty acids to the liver, inadequate fatty acid oxidation, and increased de novo lipogenesis. Insulin resistance may enhance hepatic fat accumulation by increasing free fatty acid delivery and by the effect of hyperinsulinemia to stimulate anabolic processes. The impact of weight loss, metformin, and thiazolidinediones, all treatments aimed at improving insulin sensitivity, as well as other agents such as vitamin E, have been evaluated in patients with NAFLD and have shown some benefit. However, most intervention studies have been small and uncontrolled.

Conclusion: Insulin resistance is a major feature of NAFLD that, in some patients, can progress to steatohepatitis. Treatments aimed at reducing insulin resistance have had some success, but larger placebo-controlled studies are needed to fully establish the efficacy of these interventions and possibly others in reducing the deleterious effects of fat accumulation in the liver.

Publication types

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

MeSH terms

  • Cytokines / physiology
  • Fatty Acids / analysis
  • Fatty Liver / epidemiology
  • Fatty Liver / etiology*
  • Fatty Liver / therapy
  • Humans
  • Inflammation / complications
  • Inflammation / etiology
  • Insulin Resistance / physiology*
  • Liver / chemistry
  • Obesity / complications
  • Obesity / etiology

Substances

  • Cytokines
  • Fatty Acids