Pourahmadi Mohammad, Erfanian Saiedeh, Moradzadeh Malihe, Jahromi Abdolreza Sotoodeh
Department of Anatomy, Jahrom University of Medical Sciences, Jahrom, Iran.
Research Center for Non-Communicable Diseases, Jahrom University of Medical Sciences, Jahrom, Iran.
Diabetes Metab J. 2015 Dec;39(6):512-7. doi: 10.4093/dmj.2015.39.6.512. Epub 2015 Nov 13.
Transcription factor 7-like 2 (TCF7L2) is a transcription factor in the Wnt signaling pathway. High levels of TCF7L2 have been reported in most human tissues, including the heart, lung, brain, liver, kidney, placenta, adipose tissues, and pancreatic β-cells. The purpose of this study was to assess the association between TCF7L2 polymorphisms (rs12255372 and rs7903146) and type 2 diabetes mellitus in the city of Jahrom, Iran.
This case-control study was conducted with 200 patients referred to Diabetes Clinics and 200 healthy subjects in Jahrom City. Biochemical characteristics were first determined. TCF7L2 rs1255372 and rs7903146 polymorphisms were then genotyped using the polymerase chain reaction-restriction fragment length polymorphism method.
T-allele frequencies of both single nucleotide polymorphisms (SNPs) were significantly higher in diabetic patients than in normal glucose-tolerant subjects (rs12255372: 20.3% vs. 14.5%; rs7903146: 28.5% vs. 22.25%). The rs12255372 (G/T) polymorphism analysis showed an odds ratio of 0.473 (95% confidence interval [CI], 0.170 to 1.314; P=0.151) for the TT genotype and 0.646 (95% CI, 0.410 to 1.019; P=0.060) for the TG genotype, compared with the GG genotype. The rs7903146 (C/T) polymorphism odds ratios for TT and TC genotypes were 0.564 (95% CI, 0.280 to 1.135; P=0.109) and 0.751 (95% CI, 0.487 to 1.157; P=0.194) compared with the CC genotype, respectively.
The rs12255372 and rs7903146 SNPs of the TCF7L2 gene were not associated with insulin resistance in the evaluated population.
转录因子7样2(TCF7L2)是Wnt信号通路中的一种转录因子。据报道,在大多数人体组织中,包括心脏、肺、脑、肝、肾、胎盘、脂肪组织和胰腺β细胞,TCF7L2水平较高。本研究的目的是评估伊朗贾赫罗姆市TCF7L2基因多态性(rs12255372和rs7903146)与2型糖尿病之间的关联。
本病例对照研究对转诊至贾赫罗姆市糖尿病诊所的200例患者和200名健康受试者进行。首先测定生化特征。然后采用聚合酶链反应-限制性片段长度多态性方法对TCF7L2 rs1255372和rs7903146基因多态性进行基因分型。
糖尿病患者中两种单核苷酸多态性(SNP)的T等位基因频率均显著高于糖耐量正常的受试者(rs12255372:20.3%对14.5%;rs7903146:28.5%对22.25%)。与GG基因型相比,rs12255372(G/T)基因多态性分析显示,TT基因型的比值比为0.473(95%置信区间[CI],0.170至1.314;P=0.151),TG基因型的比值比为0.646(95%CI,0.410至1.019;P=0.060)。与CC基因型相比,rs7903146(C/T)基因多态性中TT和TC基因型的比值比分别为0.564(95%CI,0.280至1.135;P=0.109)和0.751(95%CI,0.487至1.157;P=0.194)。
在评估人群中,TCF7L2基因的rs12255372和rs7903146 SNP与胰岛素抵抗无关。