Combinations of alcohol-induced flushing with genetic polymorphisms of alcohol and aldehyde dehydrogenases and the risk of alcohol dependence in Japanese men and women

• Published in: PloS one 2021-07, Vol.16 (7), p.e0255276-e0255276
• Main Authors: Yokoyama, Akira, Yokoyama, Tetsuji, Kimura, Mitsuru, Matsushita, Sachio, Yokoyama, Masako
• Format: Article
• Language: English
• Subjects: Addictions; Age; Alcohol; Alcohol dehydrogenase; Alcohol use; Alcoholic beverages; Alcoholism; Aldehyde dehydrogenase; Aldehydes; Analysis; Beer; Biology and Life Sciences; Dehydrogenase; Dehydrogenases; Dependence; Drinking; Drinking behavior; Drug dependence; Evaluation; Flushing; Gene polymorphism; Genetic aspects; Genotype & phenotype; Genotypes; Genotyping; Health risks; Medicine and Health Sciences; Men; Physical Sciences; Questionnaires; Research and Analysis Methods; Risk analysis; Risk assessment; Risk factors; Social Sciences; Women
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0255276

Objective The risk of alcohol dependence (AD) in Japanese men and women was evaluated according to combinations of alcohol flushing and aldehyde dehydrogenase-2 (ALDH2, rs671) and alcohol dehydrogenase-1B (ADH1B, rs1229984) genotypes, all of which are known to determine AD susceptibility in Asians. Previous studies have focused on men, since women account for a smaller proportion of AD subjects. Methods Case control studies were conducted between 3721 male and 335 female AD Japanese and 610 male and 406 female controls who were asked about their current or former tendency to experience facial flushing after drinking a glass of beer and underwent ALDH2 and ADH1B genotyping. The time at which alcohol-induced facial flushing tendencies had disappeared in former-flushing AD subjects was also evaluated. Results Current alcohol flushing, the inactive ALDH2*1/*2 genotype, and the fast-metabolizing ADH1B*2 allele were less frequently found in the AD groups. Although alcohol flushing was strongly influenced by the ALDH2 and ADH1B genotypes, multiple logistic model showed that never or former flushing and the genotype combinations were independent strong risk factors of AD in men and women. Never or former flushing (vs. current flushing) markedly increased the odds ratios of AD in carriers of each of the ALDH2 and ADH1B genotype combinations. The temporal profiles for drinking and flushing in former-flushing AD subjects revealed that the flushing response disappeared soon after or before the start of habitual drinking during young adulthood, regardless of the ALDH2 genotype. Conclusion Although alcohol flushing is influenced by the ALDH2 and ADH1B genotypes, constitutional or acquired flushing tolerance is an independent susceptibility trait for AD. The combination of the alcohol flushing status and the ALDH2 and ADH1B genotypes can provide a better new strategy for AD risk assessment than the alcohol flushing status alone or the genotypes alone in Asian men and women.