Abstract

Although high-density lipoprotein-cholesterol (HDL-C) concentration is a negative risk factor for atherosclerotic cardiovascular disease (CVD), efforts to reduce CVD risk by raising HDL-C have not been uniformly successful. Many studies have shown that alcohol consumption, that increases plasma HDL-C concentration, reduces CVD incidence. However, recent genetic studies in large populations have not only removed HDL-C from the causal link between plasma HDL-C concentration and reduced CVD risk, but also suggest that the association is weak. We propose here that the cardioprotective effects of alcohol are mediated by the interaction of its terminal metabolite, acetate, with the adipocyte free fatty acid receptor 2 (FFAR2), which elicits a profound antilipolytic effect that may increase insulin sensitivity without necessarily raising plasma HDL-C concentration. A large body of epidemiological evidence shows that plasma HDL-C concentrations are negatively correlated with the incidence of atherosclerosis. CETP inhibitors and HDL alleles that increase plasma HDL-C concentrations do not cardioprotect. The functional qualities of HDL are more relevant to cardioprotection than plasma HDL-C concentrations.Alcohol consumption is associated with reduced cardiovascular disease without a profound increase in plasma HDL-C concentrations.Alcohol is converted to acetate, which elicits an antilipolytic effect via a G-protein coupled receptor (FFAR2). New interventions that improve HDL functionality without necessarily increasing its concentration should be identified and validated.

Original languageEnglish (US)
Pages (from-to)44-53
Number of pages10
JournalTrends in Endocrinology and Metabolism
Volume27
Issue number1
DOIs
StatePublished - Jan 1 2016

Keywords

  • Acetate
  • Alcohol
  • Atherosclerosis
  • Dyslipidemia
  • FFAR2
  • HDL

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

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