期刊文献+

TCF7L2、AKT2、FOXO1基因多态性与2型糖尿病的相关性研究 被引量:3

The Association Study between Polymorphisms of TCF7L2,AKT2 and FOXO1 Genes and Type 2 Diabetes
暂未订购
导出
摘要 目的:探讨天津地区汉族人群TCF7L2、AKT2、FOXO1基因多态性与2型糖尿病(T2DM)发生的关系。方法:选取352例T2DM患者(T2DM组)及176例健康体检者(对照组),提取基因组DNA,PCR扩增目的片段后,应用变性高效液相色谱技术检测3种基因的基因型频率,并选取不同峰型进行DNA测序。分析不同基因型频率的组间差异,并对联合基因型进行分析,Logistic回归分析影响T2DM发病的相关因素。结果:2组TCF7L2基因rs12255372、FOXO1基因rs2701891基因型及等位基因频率差异有统计学意义,2组AKT2基因rs11669332基因型及等位基因频率差异无统计学意义。TCF7L2T+/FOXO1T+、TCF7L2G+/FOXO1C+与TCF7L2G+/FOXO1T+在2组间的分布差异有统计学意义。Logistic回归分析结果示糖化血红蛋白及尿素氮升高、TCF7L2T+/FOXO1C+为T2DM的危险因素,高密度脂蛋白胆固醇水平升高为保护因素。结论:携带TCF7L2基因rs12255372位点G/T基因型与FOXO1基因rs2701891位点C/C、C/T基因型者发生T2DM的危险性增大,可能与天津地区汉族人群T2DM的发病有关,且两基因间存在一定协同作用。 Objective: To investigate the relationship between the different genetic polymorphisms of transcription factor 7-like 2(TCF7L2), protein kinase B (AKT2) and forkhead box transcription factor subgroup O1 (FOXO1) and the type 2 diabetes mellitus (T2DM) in Tianjin Han populations. Methods: Three hundred and fifty-two T2DM patients (T2DM group)and 176 healthy subjects (control group)were randomly enrolled in this study. After the genome DNA was extracted, the genotype frequency was detected using the denaturing high performance liquid chromatography. And different peaks were sequenced. Then the differences of different genotype frequencies were analyzed between the groups. The risk factors of T2DM were evaluated using logistic regression. Results: There were significant differences in genotypes and allele frequencies of TCF7L2(rs12255372)and FOXO1 (rs2701891)between two groups. There were no significant differences in the genotype and allele frequency of AKT2(rsl1669332)between two groups. There were significant differences in genotype frequencies of TCF7L2 T+/ FOXO1T+,TCF7L2 G+/ FOXO1 C+ and TCF7L2 G+/FOXO1 T+ between two groups. The logistic regression analysis showed that levels of glycosylated hemoglobin and blood urea nitrogen were increased. TCF7L2 T+/FOXO1C+ was the risk factor of T2DM, and high density lipoprotein was a protective factor of T2DM. Conclusion: The G/T genotype in the TCF7L2, C/C and C)T genotypes in the FOXO1 gene significantly contributed to T2DM susceptibility in Tianjin Han populations. A combined effect could be found between TCFTL2 and FOXO1.
出处 《天津医药》 CAS 北大核心 2012年第12期1188-1192,共5页 Tianjin Medical Journal
关键词 糖尿病 2型 多态现象 遗传 TCF7L2 AKT2 FOXO1 天津 汉族 diabetes mellitus, type. 2 polymorphism, genetic TCF7L2 AKT2 FOXO1 TIANJIN HANNATIONALITY
  • 相关文献

参考文献1

二级参考文献20

  • 1Garofalo RS, Orena S J, Rafidi K, Torchia AJ, Stock JL, Hildebrandt AL, et al. Severe diabetes, age-dependent loss of adipose tissue, and mild growth deficiency in mice lacking Akt2/PKB beta. J Clin Invest 2003; 112: 197-208.
  • 2Cho H, Mu J, Kim JK, Thorvaldsen JL, Chu QW, Crenshaw IlI EB, et al. Insulin resistance and a diabetes meUitus-like syndrome in mice lacking the protein kinase Akt 2 (PKB β). Science 2001; 292: 1728-1731.
  • 3Liao J, Barthel A, Nakatani K, Roth RA. Activation of protein kinase B/Akt is sufficient to repress the glucocorticoid and cAMP induction of phosphoenolpyruvate carboxykinase gene. J Biol Chem 1998; 273: 27320-27324.
  • 4Kohn AD, Summers SA, Birnbaum MJ, Roth RA. Expression of a constitutively active Akt Ser/Thr kinase in 3T3-L1 adipocytes stimulates glucose uptake and glucose transporter 4 translocation. J Biol Chem 1996; 271: 31372-31378.
  • 5Ueki K, Yamamoto-Honda R, Kaburagi Y, Yamauchi T, Tobe K, Burgering BM, et al. Potential role of protein kinase B in insulin-induced glucose transport, glycogen synthesis, and protein synthesis. J Biol Chem 1998; 273: 5315-5322.
  • 6Brozinick JT Jr, Birnbaum MJ. Insulin, but not contraction, activates Akt/PKB in isolated rat skeletal muscle. J Biol Chem 1998; 273: 14679-14682.
  • 7Taniguchi CM, Emanuelli B, Kahn CR. Critical nodes in signaling pathways: insights into insulin action. Nat Rev Mol Cell Biol 2006; 7: 85-96.
  • 8Calera MR, Martinez C, Liu H, Jack AK, Birnbaum MJ, Pilch PF. Insulin increases the association of Akt-2 with Glut4- containing vesicles. J Biol Chem 1998; 273: 7201-7204.
  • 9George S, Rochford JJ, Wolfrum C, Gray SL, Schinner S, Wilson JC, et al. A family with severe insulin resistance and diabetes due to a mutation in AKT2. Science 2004; 304: 1325-1328.
  • 10Tan K, Kimber WA, Luan J, Soos MA, Semple RK, Wareham NJ, et al. Analysis of genetic variation in Akt2/PKB-β in severe insulin resistance, lipodystrophy, type 2 diabetes, and related metabolic pbenotypes. Diabetes 2007; 56: 714-719.

共引文献1

同被引文献29

引证文献3

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部