Epicardial Fat in Nonalcoholic Fatty Liver Disease: Properties and Relationships With Metabolic Factors, Cardiac Structure, and Cardiac Function

Angiology. 2016 Jan;67(1):41-8. doi: 10.1177/0003319715576672. Epub 2015 Mar 29.

Abstract

Nonalcoholic fatty liver disease (NAFLD) is closely related to insulin resistance and the metabolic syndrome and might be an important cardiovascular (CV) risk factor. Epicardial adipose tissue (EAT) has been implicated in the pathogenesis of obesity-related CV disease. In an NAFLD population, we investigated EAT thickness and its possible relations to NAFLD and cardiac structure and function. This was an observational study of 57 patients with NAFLD and 48 age-matched controls. Patients with NAFLD had significantly higher body mass index (P < .0001), waist circumference (P < .0001), and high-sensitivity C-reactive protein (P = .005), whereas high-density lipoprotein cholesterol (P = .01) and adiponectin (P = .005) levels were significantly lower. The EAT was not thicker in NAFLD but was positively related to indices of impaired glucose tolerance and inflammation, with diabetes being an independent predictor of EAT thickness (b* = 0.29, P = .04). No relations were found between EAT and cardiac structure and function. In conclusion, this study confirms a pathologic phenotype of NAFLD. Epicardial fat was not significantly related to NAFLD per se, but diabetes, glucose metabolism, and inflammation were closely related to its thickness.

Keywords: NAFLD; epicardial fat; fatty liver; metabolic syndrome.

Publication types

  • Observational Study

MeSH terms

  • Adipose Tissue / diagnostic imaging*
  • Cross-Sectional Studies
  • Echocardiography
  • Female
  • Heart Atria / diagnostic imaging*
  • Humans
  • Male
  • Metabolic Syndrome / complications
  • Metabolic Syndrome / diagnosis*
  • Metabolic Syndrome / physiopathology
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease / complications
  • Non-alcoholic Fatty Liver Disease / diagnosis*
  • Non-alcoholic Fatty Liver Disease / physiopathology
  • Pericardium / diagnostic imaging*
  • Risk Factors
  • Ventricular Function, Left / physiology*