Nishiyori Atsushi, Shibata Akira, Ogimoto Itsuro, Uchimura Naohisa, Egami Hideki, Nakamura Jun, Sakata Ritsu, Fukuda Katsuhiro
Department of Public Health, Kurume University School of Medicine, Kurume, Japan.
Psychiatry Clin Neurosci. 2005 Feb;59(1):38-44. doi: 10.1111/j.1440-1819.2005.01329.x.
The development of alcohol use disorder (AUD) is related to various social, economic, cultural, environmental and hereditary factors. Several potential risk factors have been proposed for AUD in addition to alcohol consumption, including alcohol dehydrogenase2 (ADH2), acetaldehyde dehydrogenase2 (ALDH2), marital status, educational, occupational or past medical history (e.g. diabetes mellitus, hypertension, lung, digestive tract, or chronic liver disease) or smoking habits. The present study was performed to investigate the relationship between the aforementioned potential risk factors and AUD in Japan. A case-control study was performed on 153 male Japanese AUD patients and age-, gender-, or other confounder-matched controls to investigate the relation multivariately between ADH2, ALDH2 or alcohol drinking and AUD. Genomic DNA were extracted from nail clippings by the guanidium method, and genotyping of ADH2 and ALDH2 were performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methods. Univariate analyses by the conditional logistic regression model revealed statistically significant odds ratios due to ADH21/1 genotype, ALDH21/1 genotype, middle school as the final school attended, longest occupations as farmers, fishermen, craftsmen, miners, production process or construction workers, and past histories of chronic liver disease and AUD. However, multivariate analyses under a hierarchically well-formulated model strategy with interaction and confounding assessment indicated that (i) heavy alcohol intake was a significant risk factor (odds ratio per 1.0 g of daily ethanol intake; 1.096, 95% confidence interval; 1.026-1.171) for developing AUD after adjusting for other confounders; and (ii) ADH21/1 genotype and ALDH21/1 genotype were not risk factors after adjusting for daily ethanol intake and other confounders. The present study shows that AUD was more directly and strongly associated with alcohol drinking than with alcohol metabolizing enzymes among male Japanese.
酒精使用障碍(AUD)的发展与多种社会、经济、文化、环境和遗传因素有关。除饮酒外,已提出了几种AUD的潜在风险因素,包括乙醇脱氢酶2(ADH2)、乙醛脱氢酶2(ALDH2)、婚姻状况、教育程度、职业或既往病史(如糖尿病、高血压、肺部、消化道或慢性肝病)或吸烟习惯。本研究旨在调查日本上述潜在风险因素与AUD之间的关系。对153名日本男性AUD患者和年龄、性别或其他混杂因素匹配的对照组进行了病例对照研究,以多变量研究ADH2、ALDH2或饮酒与AUD之间的关系。采用胍法从指甲剪屑中提取基因组DNA,并使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对ADH2和ALDH2进行基因分型。条件逻辑回归模型的单变量分析显示,由于ADH21/1基因型、ALDH21/1基因型、初中为最终就读学校、最长职业为农民、渔民、工匠、矿工、生产过程或建筑工人以及慢性肝病和AUD的既往史,比值比具有统计学意义。然而,在具有相互作用和混杂评估的分层良好制定的模型策略下进行的多变量分析表明:(i)在调整其他混杂因素后,大量饮酒是发生AUD的显著风险因素(每日乙醇摄入量每增加1.0 g的比值比;1.096,95%置信区间;1.026-1.171);(ii)在调整每日乙醇摄入量和其他混杂因素后,ADH21/1基因型和ALDH21/1基因型不是风险因素。本研究表明,在日本男性中,AUD与饮酒的直接和强烈关联程度高于与酒精代谢酶的关联程度。