Causal associations of alcohol consumption with cardiovascular diseases and all-cause mortality among Chinese males

Am J Clin Nutr. 2022 Sep 2;116(3):771-779. doi: 10.1093/ajcn/nqac159.

Abstract

Background: The causal effects of moderate alcohol consumption on cardiovascular diseases (CVDs) are continuously debated, especially on coronary artery disease (CAD).

Objectives: We aimed to explore the causal associations of alcohol consumption with CVDs and all-cause mortality among Chinese males.

Methods: A prospective cohort study was conducted in 40,386 Chinese males, with 17,676 being genotyped for the rs671 variant in the aldehyde dehydrogenase 2 (ALDH2) gene. A Cox proportional hazards model was conducted to estimate the effects of self-reported alcohol consumption. Mendelian randomization (MR) analysis was performed to explore the causality using rs671 as an instrumental variable.

Results: During the follow-up of 303,353 person-years, 2406 incident CVDs and 3195 all-cause mortalities were identified. J-shaped associations of self-reported alcohol consumption with incident CVD and all-cause mortality were observed, showing decreased risks for light (≤25 g/d) and moderate drinkers (25-≤60 g/d). However, MR analyses revealed a linear association of genetically predicted alcohol consumption with the incident CVD (P-trend = 0.02), including both CAD (P-trend = 0.03) and stroke (P-trend = 0.02). The HRs (95% CIs) for incident CVD across increasing tertiles of genetically predicted alcohol consumption were 1 (reference), 1.18 (1.01, 1.38), and 1.22 (1.03, 1.46). After excluding heavy drinkers, the risk of incident CVD and all-cause mortality was increased by 27% and 20% per standard drink increment of genetically predicted alcohol consumption, respectively.

Conclusions: Our analyses extend the evidence of the harmful effect of alcohol consumption to total CVD (including CAD) and all-cause mortality, highlighting the potential health benefits of lowering alcohol consumption, even among light-to-moderate male drinkers.

Keywords: Mendelian randomization; alcohol consumption; all-cause mortality; cardiovascular disease; cohort.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking* / epidemiology
  • Alcohol Drinking* / genetics
  • Aldehyde Dehydrogenase, Mitochondrial / genetics
  • Asian People / genetics
  • China / epidemiology
  • Coronary Artery Disease* / epidemiology
  • Coronary Artery Disease* / genetics
  • Humans
  • Male
  • Prospective Studies

Substances

  • ALDH2 protein, human
  • Aldehyde Dehydrogenase, Mitochondrial