Abstract

ObjectiveCoronary artery disease (CAD) is a multifactorial and polygenic disease. The aim of this study was to examine the association between six polymorphisms of four alcohol metabolism relevant genes (ADH1B, ADH1C, ALDH1b1, ALDH2) and the risk of CAD in Han Chinese.Methods and ResultsThis was a hospital-based case-control study involving 1365 hypertensive patients. All study subjects were angiographically confirmed. Genotypes were determined with ligase detection reaction method. There was no observable deviation from the Hardy-Weinberg equilibrium for six examined polymorphisms in controls. The genotype and allele distributions of ALDH1b1 rs2073478 and ALDH2 rs671 polymorphisms differed significantly between the two groups (P≤0.005), even after the Bonferroni correction. The most common allele combination was A-C-C-G-C-G (alleles in order of rs1229984, rs1693482, rs2228093, rs2073478, rs886205, rs671) and its frequency was slightly higher in controls than in CAD patients (P = 0.067). After assigning the most common allele combination as a reference, allele combination A-C-C-T-C-A, which simultaneously possessed the risk alleles of rs2073478 and rs671 polymorphisms, was associated with a 1.80-fold greater risk of CAD. Further, a two-locus model including rs2073478 and rs671 that had a maximal testing accuracy of 0.598 and a cross-validation consistency of 10 (P = 0.008) was deemed as the overall best MDR model, which was further validated by classical Logistic regression model.ConclusionOur findings provide clear evidence for both individual and interactive associations of ALDH1b1 and ALDH2 genes with the development of CAD in Han Chinese.

Highlights

  • Coronary artery disease (CAD) is a complex disease with the interplay of multiple genetic and environmental factors precipitating its development [1]

  • Given the fact that some individuals are more susceptible to CAD than others, it is of great importance to explain this inter-individual divergence in disease susceptibility in order to develop a better means for disease prediction, monitoring and personalized treatments

  • A major pathway for alcohol metabolism involves alcohol dehydrogenate (ADH) that catalyzes the oxidation of ethanol to acetaldehyde, and acetaldehyde dehydrogenase (ALDH) that further catalyzes the oxidation of acetaldehyde to acetate

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Summary

Introduction

Coronary artery disease (CAD) is a complex disease with the interplay of multiple genetic and environmental factors precipitating its development [1]. Given the fact that some individuals are more susceptible to CAD than others, it is of great importance to explain this inter-individual divergence in disease susceptibility in order to develop a better means for disease prediction, monitoring and personalized treatments. In this regard, Lieb and Vasan have written an overarching review on the genetic underpinnings of CAD [4]; there is no universal consensus on a certain gene or locus being definitively implicated in the pathogenesis of CAD. This irreproducibility might arise from population-specific genetic heterogeneity, uncontrolled confounding and statistical underpower

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