Hepatic, lipid and genetic factors associated with obesity: crosstalk with alcohol dependence?

World J Biol Psychiatry. 2017 Mar;18(2):120-128. doi: 10.1080/15622975.2016.1249952. Epub 2016 Dec 1.

Abstract

Objectives: Alcohol dependence represents a leading cause of mortality and morbidity. Understanding the variables that contribute to this diagnosis and its severity is critical. An overlap between factors that may predispose people to become obese and those that may increase the risk of alcohol dependence may exist. However, data in the literature are not conclusive. Therefore, this study aimed to identify the association between alcohol dependence and obesity-related factors, including biochemical and genetic factors.

Methods: In a case-control study with 829 participants, factors involved with metabolism and obesity were assessed, including biochemical lipid and liver markers, and the fat mass and obesity-associated (FTO) single nucleotide polymorphism (SNP) rs8050136.

Results: Increased triglycerides, having one or two minor A alleles for rs8050136 and being a smoker were associated with increased risk of alcohol dependence, while increased low-density lipoprotein cholesterol was associated with decreased risk. In addition, having abnormal gamma-glutamyl transferase and being female were factors associated with an increased severity of alcohol dependence.

Conclusions: Our preliminary findings suggest a link between alcohol dependence and obesity-related biochemical and genetic factors. Future studies are needed to better understand if these factors may play a predictive role and/or may act as biomarkers for treatment response.

Keywords: FTO; Obesity; alcohol dependence; genetics; metabolism.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Alcoholism / complications*
  • Alcoholism / genetics*
  • Alleles
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO / genetics*
  • Case-Control Studies
  • Cholesterol, LDL / blood
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Linear Models
  • Lipids / blood*
  • Logistic Models
  • Male
  • Middle Aged
  • Obesity / genetics*
  • Polymorphism, Single Nucleotide
  • Risk Factors
  • Severity of Illness Index
  • United States
  • Young Adult

Substances

  • Cholesterol, LDL
  • Lipids
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human