Gong Lilin, Li Rong, Ren Wei, Wang Zengchan, Wang Zhihong, Yang Maosheng, Zhang Suhua
Department of Endocrinology, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Laboratory for Disease and Gene, Key Laboratory of Molecular Biology of Infectious Diseases designated by the Chinese Ministry of Education, Department of Public Health, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
J Korean Med Sci. 2017 Feb;32(2):264-271. doi: 10.3346/jkms.2017.32.2.264.
Here, we aimed to study the effect of the forkhead box O1-insulin receptor substrate 2 (FOXO1-IRS2) gene interaction and the FOXO1 and IRS2 genes-environment interaction for the risk of type 2 diabetes mellitus (T2DM) in a Chinese Han population. We genotyped 7 polymorphism sites of FOXO1 gene and IRS2 gene in 780 unrelated Chinese Han people (474 cases of T2DM, 306 cases of healthy control). The risk of T2DM in individuals with AA genotype for rs7986407 and CC genotype for rs4581585 in FOXO1 gene was 2.092 and 2.57 times higher than that with GG genotype (odds ratio [OR] = 2.092; 95% confidence interval [CI] = 1.178-3.731; P = 0.011) and TT genotype (OR = 2.571; 95% CI = 1.404-4.695; P = 0.002), respectively. The risk of T2DM in individuals with GG genotype for Gly1057Asp in IRS2 gene was 1.42 times higher than that with AA genotype (OR = 1.422; 95% CI = 1.037-1.949; P = 0.029). The other 4 single nucleotide polymorphisms (SNPs) had no significant association with T2DM (P > 0.05). Multifactor dimensionality reduction (MDR) analysis showed that the interaction between SNPs rs7986407 and rs4325426 in FOXO1 gene and waist was the best model confirmed by interaction analysis, closely associating with T2DM. There was an increased risk for T2DM in the case of non-obesity with genotype combined AA/CC, AA/AC or AG/AA for rs7986407 and rs4325426, and obesity with genotype AA for rs7986407 or AA for rs4325426 (OR = 3.976; 95% CI = 1.156-13.675; P value from sign test [P(sign)] = 0.025; P value from permutation test [P(perm)] = 0.000-0.001). Together, this study indicates an association of FOXO1 and IRS2 gene polymorphisms with T2DM in Chinese Han population, supporting FOXO1-obesity interaction as a key factor for the risk of T2DM.
在此,我们旨在研究叉头框O1-胰岛素受体底物2(FOXO1-IRS2)基因相互作用以及FOXO1和IRS2基因与环境的相互作用对中国汉族人群2型糖尿病(T2DM)发病风险的影响。我们对780名无亲缘关系的中国汉族人(474例T2DM患者,306例健康对照)的FOXO1基因和IRS2基因的7个多态性位点进行了基因分型。FOXO1基因中rs7986407位点AA基因型个体和rs4581585位点CC基因型个体患T2DM的风险分别是GG基因型个体的2.092倍和2.57倍(优势比[OR]=2.092;95%置信区间[CI]=1.178 - 3.731;P = 0.011)以及TT基因型个体的2.571倍(OR = 2.571;95% CI = 1.404 - 4.695;P = 0.002)。IRS2基因Gly1057Asp位点GG基因型个体患T2DM的风险是AA基因型个体的1.42倍(OR = 1.422;95% CI = 1.037 - 1.949;P = 0.029)。其他4个单核苷酸多态性(SNP)与T2DM无显著关联(P>0.05)。多因素降维(MDR)分析表明,FOXO1基因中的SNP rs7986407和rs4325426与腰围之间的相互作用是经相互作用分析确认的最佳模型,与T2DM密切相关。对于rs7986407和rs4325426,非肥胖个体中基因型组合为AA/CC、AA/AC或AG/AA以及肥胖个体中rs7986407基因型为AA或rs4325426基因型为AA时,T2DM发病风险增加(OR = 3.976;95% CI = 1.156 - 13.675;符号检验P值[P(sign)] = 0.025;置换检验P值[P(perm)] = 0.000 - 0.001)。总之,本研究表明中国汉族人群中FOXO1和IRS2基因多态性与T2DM有关联,支持FOXO1 - 肥胖相互作用是T2DM发病风险的关键因素。