Idewaki Yasuhiro, Iwase Masanori, Fujii Hiroki, Ohkuma Toshiaki, Ide Hitoshi, Kaizu Shinako, Jodai Tamaki, Kikuchi Yohei, Hirano Atsushi, Nakamura Udai, Kubo Michiaki, Kitazono Takanari
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Diabetes Center, Hakujyuji Hospital, Fukuoka, Japan.
PLoS One. 2015 Nov 23;10(11):e0143288. doi: 10.1371/journal.pone.0143288. eCollection 2015.
Aldehyde dehydrogenase 2 (ALDH2) detoxifies aldehyde produced during ethanol metabolism and oxidative stress. A genetic defect in this enzyme is common in East Asians and determines alcohol consumption behaviors. We investigated the impact of genetically determined ALDH2 activity on diabetic microvascular and macrovascular complications in relation to drinking habits in Japanese patients with type 2 diabetes mellitus. An ALDH2 single-nucleotide polymorphism (rs671) was genotyped in 4,400 patients. Additionally, the relationship of clinical characteristics with ALDH2 activity (ALDH2 *1/*1 active enzyme activity vs. *1/*2 or *2/*2 inactive enzyme activity) and drinking habits (lifetime abstainers vs. former or current drinkers) was investigated cross-sectionally (n = 691 in *1/*1 abstainers, n = 1,315 in abstainers with *2, n = 1,711 in *1/*1 drinkers, n = 683 in drinkers with *2). The multiple logistic regression analysis for diabetic complications was adjusted for age, sex, current smoking habits, leisure-time physical activity, depressive symptoms, diabetes duration, body mass index, hemoglobin A1c, insulin use, high-density lipoprotein cholesterol, systolic blood pressure and renin-angiotensin system inhibitors use. Albuminuria prevalence was significantly lower in the drinkers with *2 than that of other groups (odds ratio [95% confidence interval (CI)]: *1/*1 abstainers as the referent, 0.94 [0.76-1.16] in abstainers with *2, 1.00 [0.80-1.26] in *1/*1 drinkers, 0.71 [0.54-0.93] in drinkers with *2). Retinal photocoagulation prevalence was also lower in drinkers with ALDH2 *2 than that of other groups. In contrast, myocardial infarction was significantly increased in ALDH2 *2 carriers compared with that in ALDH2 *1/*1 abstainers (odds ratio [95% CI]: *1/*1 abstainers as the referent, 2.63 [1.28-6.13] in abstainers with *2, 1.89 [0.89-4.51] in *1/*1 drinkers, 2.35 [1.06-5.79] in drinkers with *2). In summary, patients with type 2 diabetes and ALDH2 *2 displayed a lower microvascular complication prevalence associated with alcohol consumption but a higher macrovascular complication prevalence irrespective of alcohol consumption.
乙醛脱氢酶2(ALDH2)可使乙醇代谢和氧化应激过程中产生的乙醛解毒。这种酶的基因缺陷在东亚人中很常见,并决定饮酒行为。我们研究了基因决定的ALDH2活性对日本2型糖尿病患者糖尿病微血管和大血管并发症的影响,并与饮酒习惯相关联。对4400例患者进行了ALDH2单核苷酸多态性(rs671)基因分型。此外,还对临床特征与ALDH2活性(ALDH2 *1/1活性酶活性与1/2或2/*2无活性酶活性)和饮酒习惯(终生戒酒者与既往或当前饮酒者)之间的关系进行了横断面研究(*1/*1戒酒者中有691例,*2戒酒者中有1315例,*1/*1饮酒者中有1711例,*2饮酒者中有683例)。对糖尿病并发症的多因素逻辑回归分析对年龄、性别、当前吸烟习惯、休闲时间体育活动、抑郁症状、糖尿病病程、体重指数、糖化血红蛋白、胰岛素使用、高密度脂蛋白胆固醇、收缩压和肾素-血管紧张素系统抑制剂使用进行了校正。2饮酒者的白蛋白尿患病率显著低于其他组(优势比[95%置信区间(CI)]:以1/*1戒酒者为参照,*2戒酒者为0.94[0.76-1.16],*1/*1饮酒者为1.00[0.80-1.26],*2饮酒者为0.71[0.54-0.93])。ALDH2 *2饮酒者的视网膜光凝患病率也低于其他组。相比之下,与ALDH2 *1/*1戒酒者相比,ALDH2 2携带者的心肌梗死显著增加(优势比[95%CI]:以1/*1戒酒者为参照,*2戒酒者为2.63[1.28-6.13],*1/*1饮酒者为1.89[0.89-4.51],*2饮酒者为2.35[1.06-5.79])。总之,2型糖尿病和ALDH2 *2患者饮酒相关的微血管并发症患病率较低,但无论饮酒与否,大血管并发症患病率较高。