a Department of Preventive Medicine, Shenzhen University School of Medicine, 3688 Nanhai Road, Shenzhen, 518060, China.
b Department of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Appl Physiol Nutr Metab. 2017 Dec;42(12):1316-1321. doi: 10.1139/apnm-2017-0232. Epub 2017 Aug 14.
The impact of gene-environment interaction on diabetes remains largely unknown. We aimed to investigate if interaction between glucose metabolizing genes and lifestyle factors is associated with type 2 diabetes mellitus (T2DM). Interactions between genotypes of 4 glucose metabolizing genes (MTNR1B, KCNQ1, KLF14, and GCKR) and lifestyle factors were estimated in 722 T2DM patients and 759 controls, using multiple logistic regression. No significant associations with T2DM were detected for the single nucleotide polymorphisms of MTNR1B, KLF14 and GCKR. However, rs151290 (KCNQ1) polymorphisms were found to be associated with risk of T2DM. Compared with AA, the odds ratios (ORs) of AC or CC genotypes for developing T2DM were 1.545 (P = 0.0489) and 1.603 (P = 0.0383), respectively. In stratified analyses, the associations were stronger in smokers with CC than smokers with AA (OR = 3.668, P = 0.013); drinkers with AC (OR = 5.518, P = 0.036), CC (OR = 8.691, P = 0.0095), and AC+CC (OR = 6.764, P = 0.016) than drinkers with AA. Compared with nondrinkers with AA, drinkers who carry AC and CC had 12.072-fold (P = 0.0007) and 8.147-fold (P = 0.0052) higher risk of developing T2DM. In conclusions, rs151290 (KCNQ1) polymorphisms are associated with increased risk of T2DM, alone and especially in interaction with smoking and alcohol.
基因-环境相互作用对糖尿病的影响在很大程度上尚不清楚。我们旨在研究葡萄糖代谢基因与生活方式因素之间的相互作用是否与 2 型糖尿病(T2DM)有关。在 722 例 T2DM 患者和 759 例对照中,使用多元逻辑回归估计了 4 种葡萄糖代谢基因(MTNR1B、KCNQ1、KLF14 和 GCKR)的基因型与生活方式因素之间的相互作用。MTNR1B、KLF14 和 GCKR 的单核苷酸多态性与 T2DM 无显著相关性。然而,发现 rs151290(KCNQ1)多态性与 T2DM 的发病风险相关。与 AA 相比,AC 或 CC 基因型发生 T2DM 的优势比(OR)分别为 1.545(P = 0.0489)和 1.603(P = 0.0383)。在分层分析中,CC 基因型的吸烟者比 AA 基因型的吸烟者的关联更强(OR = 3.668,P = 0.013);AC 基因型的饮酒者(OR = 5.518,P = 0.036),CC 基因型的饮酒者(OR = 8.691,P = 0.0095)和 AC+CC 基因型的饮酒者(OR = 6.764,P = 0.016)比 AA 基因型的饮酒者更强。与 AA 基因型的非饮酒者相比,携带 AC 和 CC 基因型的饮酒者发生 T2DM 的风险分别增加了 12.072 倍(P = 0.0007)和 8.147 倍(P = 0.0052)。总之,rs151290(KCNQ1)多态性与 T2DM 的发病风险增加有关,单独存在时尤其如此,尤其是与吸烟和饮酒相互作用时。