Department of Internal Medicine, Seoul National University Bundang Hospital, Seoungnam, Gyeonggi-do, Korea.
Int J Epidemiol. 2011 Aug;40(4):1047-55. doi: 10.1093/ije/dyr067. Epub 2011 Apr 19.
The relationship between alcohol intake and the risk for gastric cancer is not fully understood. The association between alcohol consumption and the risk for gastric cancer was investigated in the Korean population with the ALDH2 genotype.
From 2003 to 2008, 445 patients with gastric cancer and 370 control subjects ≥ 50 years of age were included in the analysis. Logistic regression models including age, gender, education, smoking and drinking status, Helicobacter pylori infection and ALDH2 genotype were evaluated to estimate the adjusted odds ratios (ORs) for the development of gastric cancer.
For all subjects, the risk for gastric cancer was increased in ex-drinkers [OR 1.68, 95% confidence interval (CI) 1.07-2.64], but not in current drinkers. Subjects with inactive ALDH2 *2 allele(s) showed a lower level of alcohol consumption than ALDH2 *1/*1 homozygotes (P < 0.001). Among the ALDH2 *1/*2 carriers (n = 243), current/ex-drinkers had a significantly increased risk for gastric cancer compared with never/rare drinkers (OR 2.80, 95% CI 1.51-5.19). Among heavy drinkers (n = 115), ALDH2 *1/*2 heterozygotes had a 4-fold increased risk for gastric cancer compared with *1/*1 homozygotes (OR 4.26, 95% CI 1.10-16.47); however, no risk increase was seen among never/rare drinkers.
A dose-response association between alcohol intake and the risk for gastric cancer was not observed. However, ALDH2 polymorphisms were found to modify the susceptibility to the development of gastric cancer associated with alcohol intake, especially in case of ALDH2 *1/*2 genotype. The findings suggest an alcohol-ALDH2 genotype interaction in gastric carcinogenesis.
饮酒与胃癌风险之间的关系尚未完全阐明。本研究旨在探讨韩国人群中乙醛脱氢酶 2(ALDH2)基因型与酒精摄入和胃癌风险之间的关系。
2003 年至 2008 年,纳入了 445 例胃癌患者和 370 例年龄≥50 岁的对照组。采用包含年龄、性别、教育程度、吸烟和饮酒状况、幽门螺杆菌感染和 ALDH2 基因型等因素的 logistic 回归模型来评估胃癌发生的调整比值比(OR)。
对于所有受试者,饮酒者(OR 1.68,95%置信区间[CI]:1.07-2.64)发生胃癌的风险增加,但当前饮酒者除外。无活性 ALDH22 等位基因(ALDH22)携带者的饮酒量低于 ALDH2*1/1 纯合子(P<0.001)。在 ALDH21/2 携带者(n=243)中,当前/既往饮酒者发生胃癌的风险明显高于从不/偶尔饮酒者(OR 2.80,95%CI:1.51-5.19)。在重度饮酒者(n=115)中,ALDH21/2 杂合子发生胃癌的风险是 ALDH21/*1 纯合子的 4 倍(OR 4.26,95%CI:1.10-16.47);然而,从不/偶尔饮酒者未见风险增加。
本研究未观察到饮酒量与胃癌风险之间呈剂量反应关系。然而,ALDH2 多态性可改变与饮酒相关的胃癌易感性,尤其是在 ALDH2*1/*2 基因型中。这些发现提示酒精与 ALDH2 基因型在胃癌发生过程中存在交互作用。