Joint effect of longevity-associated mitochondrial DNA 5178 C/A polymorphism and alcohol consumption on risk of hyper-LDL cholesterolemia in middle-aged Japanese men

Lipids Health Dis. 2011 Jun 25:10:105. doi: 10.1186/1476-511X-10-105.

Abstract

Background: Combined effects between mitochondrial DNA 5178 (Mt5178) C/A polymorphism and alcohol consumption on the risk of hypertension or hyperuricemia have been reported. The objective of this study was to investigate whether Mt5178 C/A polymorphism modulates the effects of alcohol consumption on the risk of dyslipidemia.

Methods: A total of 394 male subjects were selected from among individuals visiting the hospital for regular medical check-ups. After Mt5178 C/A genotyping, a cross-sectional study assessing the combined effect of Mt5178 polymorphism and alcohol consumption on the risk of dyslipidemia was conducted.

Results: For men with Mt5178C, alcohol consumption was significantly and negatively associated with the risk of hyper-low-density lipoprotein (LDL) cholesterolemia (serum LDL cholesterol ≥ 140 mg/dl) (P for trend = 0.015). After adjustment for age, body mass index (BMI), habitual smoking, coffee consumption and use of antihypertensive medicine, the odds ratio (OR) for hyper-LDL cholesterolemia was significantly lower in daily drinkers with Mt5178C than non-drinkers with Mt5178C (OR = 0.360, 95% confidence intervals: 0.153-0.847). A significant and negative association between alcohol consumption and serum LDL cholesterol levels was also observed in Mt5178C genotypic men (P for trend < 0.01). On the other hand, the association between Mt5178A genotype and risk of hyper-LDL cholesterolemia does not appear to depend on alcohol consumption.

Conclusions: For Mt5178C genotypic men, alcohol consumption may reduce the risk of hyper-LDL cholesterolemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking / adverse effects*
  • Cholesterol, LDL / blood*
  • DNA, Mitochondrial / genetics*
  • Genetic Association Studies
  • Genotype
  • Humans
  • Hypercholesterolemia / epidemiology
  • Hypercholesterolemia / etiology
  • Hypercholesterolemia / genetics*
  • Japan / epidemiology
  • Logistic Models
  • Longevity / genetics*
  • Male
  • Middle Aged
  • NADH Dehydrogenase / genetics
  • Odds Ratio
  • Polymorphism, Single Nucleotide*

Substances

  • Cholesterol, LDL
  • DNA, Mitochondrial
  • NADH Dehydrogenase
  • NADH dehydrogenase subunit 2, human