Practical approach to non-alcoholic fatty liver disease in patients with diabetes

Diabet Med. 2015 Sep;32(9):1121-33. doi: 10.1111/dme.12725. Epub 2015 Mar 18.

Abstract

The prevalence of Type 2 diabetes is expected to increase in parallel with obesity rates and the ageing population. Recent studies show that Type 2 diabetes is associated with a twofold increase in the risk of non-alcoholic fatty liver disease, a leading cause of chronic liver disease. Individuals with non-alcoholic steatohepatitis, a more advanced stage of non-alcoholic fatty liver disease, are specifically at risk of developing fibrosis/cirrhosis (end-stage liver disease) and hepatocellular carcinoma; therefore, identifying individuals (with Type 2 diabetes) who are likely to develop hepatic complications is paramount. In the present clinical review, we discuss the potential impact of non-alcoholic fatty liver disease diagnosis on Type 2 diabetes, and the putative risk factors for developing non-alcoholic steatohepatitis and non-alcoholic steatohepatitis fibrosis. We highlight the limitations of currently used tools in non-alcoholic fatty liver disease diagnosis and staging, and provide an insight into future developments in the field. We present an example of a non-alcoholic fatty liver disease screening protocol and discuss the therapeutic options currently available to our patients.

Publication types

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

MeSH terms

  • Biomarkers / metabolism
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diet
  • Gastrointestinal Microbiome / physiology
  • Hepatitis / physiopathology
  • Humans
  • Hypoglycemic Agents / therapeutic use
  • Lipase / genetics
  • Liver Cirrhosis / diagnosis
  • Liver Cirrhosis / etiology
  • Membrane Proteins / genetics
  • Non-alcoholic Fatty Liver Disease / diagnosis
  • Non-alcoholic Fatty Liver Disease / etiology*
  • Non-alcoholic Fatty Liver Disease / therapy
  • Obesity / complications
  • Polymorphism, Genetic / genetics
  • Risk Factors
  • Risk Reduction Behavior
  • Treatment Outcome
  • Weight Loss / physiology

Substances

  • Biomarkers
  • Hypoglycemic Agents
  • Membrane Proteins
  • Lipase
  • adiponutrin, human