National Hospital Organization Kurihama Medical and Addiction Center, Yokosuka, Kanagawa, Japan.
Department of Health Promotion, National Institute of Public Health, Wako, Saitama, Japan.
PLoS One. 2021 Jul 26;16(7):e0255276. doi: 10.1371/journal.pone.0255276. eCollection 2021.
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.
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.
Current alcohol flushing, the inactive ALDH2*1/2 genotype, and the fast-metabolizing ADH1B2 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.
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.
根据酒精潮红和乙醛脱氢酶-2(ALDH2,rs671)和醇脱氢酶-1B(ADH1B,rs1229984)基因型的组合,评估日本男性和女性的酒精依赖(AD)风险,这些基因型都被认为决定了亚洲人的 AD 易感性。之前的研究主要集中在男性,因为女性在 AD 患者中所占比例较小。
在 3721 名男性和 335 名女性 AD 日本患者与 610 名男性和 406 名女性对照中进行病例对照研究,询问他们在喝一杯啤酒后是否有面部潮红的倾向,并进行 ALDH2 和 ADH1B 基因分型。还评估了以前有潮红的 AD 患者中,酒精诱导的面部潮红倾向消失的时间。
当前的酒精潮红、无活性的 ALDH2*1/2 基因型和快速代谢的 ADH1B2 等位基因在 AD 组中较少发现。尽管酒精潮红受 ALDH2 和 ADH1B 基因型的强烈影响,但多变量逻辑模型显示,无论男性还是女性,从不或以前有潮红和基因型组合是 AD 的独立强危险因素。从不或以前有潮红(与当前有潮红相比)显著增加了携带每种 ALDH2 和 ADH1B 基因型组合的 AD 的优势比。以前有潮红的 AD 患者的饮酒和潮红的时间曲线表明,无论 ALDH2 基因型如何,潮红反应在成年早期开始习惯性饮酒后很快或之前就消失了。
尽管酒精潮红受 ALDH2 和 ADH1B 基因型的影响,但先天或获得性潮红耐受是 AD 的独立易感性特征。与单独的酒精潮红状态或基因型相比,酒精潮红状态和 ALDH2 和 ADH1B 基因型的组合可以为亚洲男性和女性的 AD 风险评估提供更好的新策略。