期刊文献+

TCF7L2基因rs7903146T/C和rs7901695T/C单核苷酸多态性与内蒙古汉族人群2型糖尿病易感性的相关性研究 被引量:9

Study on the relation of TCF7L2 rs7903146T/C and rs7901695T/C SNPs with susceptibility to Type 2 Diabetes mellitus in Inner Mongolia Han people
原文传递
导出
摘要 目的研究内蒙古地区汉族人群中T2DM易感性与TCF7L2基因rs7903146T/C和rs7901695T/C位点单核苷酸多态性(SNPs)是否相关。方法收集T2DM患者和正常体检人群的抗凝血,采用等位基因特异性PCR(AS-PCR)进行SNPs分析;运用SHEsis软件对T2DM组和正常对照(NC)组的TCF7L2基因的SNPs位点进行连锁不平衡和单倍型分析。结果rs7903146T/C和rs7901695T/C位点的基因型分布在T2DM及NC组间的分布差异无统计学意义(P>0.05),但rs7903146T/C位点的T和C等位基因频率在两组间的分布差异有统计学意义(P<0.05)。rs7903146T/C和rs7901695T/C位点连锁平衡(D′=0.060),rs7901695T-rs7903146T单倍型在T2DM组的频率明显高于NC组(P<0.01,OR=1.803,95%CI:1.183~2.7487)。结论在内蒙古地区汉族人群,rs7903146位点C→T多态性可能与T2DM关联,携带突变等位基因T可增加罹患T2DM的风险,rs7901695位点C→T多态性与T2DM易感性无明显相关性,但rs7901695T-rs7903146T单倍型与T2DM发病风险相关。 Objective To study the susceptibility of Inner Mongolia Han people to type 2 diabetes mellitus(T2DM) and its association with the TCF7L2 rs7903146 T/C and rs7901695 T/C single nucleotide polymorphisms(SNPs).Methods The serum of T2DM patients and normal people in health examinations was collected.Allele-specific PCR was used to analyze the SNPs of TCF7L2 rs7903146 and rs7901695.SHEsis software was adopted to analyze the linkage disequilibrium(LD) and haplotype of SNPs of TCF7L2 of the subjects.Results The difference of genotype distributions of rs7903146 and rs7901695 between the T2DM and normal control(NC) groups was not statistically significant(P〉0.05),but the difference of distribution of T and C allele frequency of rs7903146 between the two groups was statistically significant(P〈0.05).The linkage equilibrium of rs7903146 T/C and rs7901695 T/C(D′=0.060) and the frequency of rs7901695T-rs7903146T haplotype in the T2DM group were significantly higher than those in the NC group(P〈0.01,OR=1.803,95%CI:1.183-2.7487). Conclusion In Inner Mongolia Han people,rs7903146 C→T polymorphism is possibly related with T2DM,and mutated T allelic gene can increase the risk to T2DM.However,rs7901695 C→T polymorphism is not significantly related the susceptibility to T2DM,while rs7901695T-rs7903146T haplotype is related with the risk of T2DM.
出处 《中国糖尿病杂志》 CAS CSCD 北大核心 2012年第10期721-724,共4页 Chinese Journal of Diabetes
基金 内蒙古自治区科技计划项目(20090501) 内蒙古自然科学基金面上项目(2009MS1120) 秦文斌科技助研基金项目(200911)
关键词 糖尿病 2型 TCF7L2 单核苷酸多态性 基因型频率 单倍型 Diabetes mellitus,type2; TCF7L2; Single nucleotide polymorphisms(SNPs); Genotype frequency; Haplotype
  • 相关文献

参考文献12

  • 1Grant S F, Thorleifsson G, Reynisdottir L Variant of tran- scriptionfactor7-1ike 2(TCF7L2)gene confers risk of type 2 di- abetes. Nat Genet, 2006, 38: 320-323.
  • 2Christopher J G, Eleftheria Z, Jayne M, et al. Association a- nalysis of 6,736 U. K. subjects provides replication and con- firms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk. Diabetes, 2006, 55: 2640-2644.
  • 3Lyssenko V, Lupi R, Marchetti P, et al. Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes. J Clin Invest, 2007, 8: 2155-2163.
  • 4Chandak G R, Janipalli C S, Bhaskar S. Common variants in the TCFTL2 gene are strongly associated with type 2 diabetes mellitus in the Indian population. Journal of Clinical Endocri- nology & Metabolism, 2007, 2: 504-510.
  • 5Laura J S, Lori L B, Cristen J W, et al. Association of Tran- scription Factor 7 Like 2 (TCF7L2) Variants With Type 2 Di- abetes in a Finnish Sample. Diabetes, 2006, 55: 2649-2653.
  • 6Hrikoshi M, Hara K, Ito C, et al. A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese population. Diabetologia, 2007, 50 : 747-751.
  • 7唐新.中国汉族人群2型糖尿病易感基因的单核苷酸多态性研究.重庆:重庆医科大学,2009.
  • 8韩丽红,王彩丽,闫斌,高丽君,秦文斌.PAI-1基因4G/5G多态性与内蒙地区IgA肾病的相关性研究[J].放射免疫学杂志,2009,22(1):74-76. 被引量:7
  • 9马聪,盛宏光.一种新的2型糖尿病易感基因:TCF7L2[J].江苏大学学报(医学版),2009,19(4):362-365. 被引量:4
  • 10Mayans S, Lackovic K, Lindgren P, et al. TCF7L2 polymor- phisms are associated with type 2 diabetes in northern Sweden. Eur J Hum Genet, 2007, 3:342-346.

二级参考文献41

  • 1丁瑞,陈香美,刘述文,吕扬,吴杰.PAI-1基因4G4G基因型与IgA肾病易感性及临床表现的关系[J].中华医学遗传学杂志,2006,23(4):449-451. 被引量:11
  • 2张帆.IgA肾病与基因多态性[J].临床和实验医学杂志,2007,6(6):171-173. 被引量:4
  • 3Teresa YHW, Peter P, Cheuk CS, et al. Association of plasminogen activator inhibitor - 1 4G/4G genotype and type 2 diabetic nephropathy in Chinese patients. Kidney International. 2000,57:632.
  • 4Jeng JR. Association of PAI- 1 gene promoter 4G/5 G polymorphism with plasma PAI - 1 activity in Chinese patients with and without hypertension. Am J Hypertens. 2003,16:290.
  • 5Matsuo S, Lopez - Guisa JM, Cai X, et al. Multifunctionality of PAI - 1 in fibrogenesis: evidence from obstructive nephropathy in PAI - 1 - overexpressing mice. Kidney Int. 2005,67:2221.
  • 6Rerolle JP, Hotly A, Nguyen G, et al. Plasminogen activator inhibitor type 1 is a potential target in renal fibrogenesis. Kidney Int. 2000,58 : 1841.
  • 7Suzuki H, Sakuma Y, Kanesaki Y, et al. Close relationship of plasminogen activator inhibitor - 1 4G/5G polymorphism and progression of IgA nephropathy. Clin Nephrol. 2004,62 : 173.
  • 8Angela YMW, Peter P, Fernand MML, et al. Plasminogen activator inhibitor- 1 gene polymorphism 4G/4G genotype and lupus nephritis in Chinese parents. Kidney International. 2001,59 : 1520.
  • 9Eddy AA. Plasminogen activator inhibitor - 1 and the kidney. Am J Physiol Renal Physiol. 2002,283(2) :209.
  • 10Grant SF, Thorleifsson G, Reynisdottir I, et al. Variant of transcription factor 7-like 2 (TCFTL2) gene confers risk of type 2 diabetes [ J ]. Nat Genet, 2006,38 ( 3 ) : 320 - 323.

共引文献9

同被引文献118

  • 1朱晖,王佑民,许敏,徐振山.转录因子7类似物2基因rs11196205多态性与安徽地区2型糖尿病及糖调节受损的相关性[J].中华糖尿病杂志,2010,2(3). 被引量:3
  • 2王盛花,贾雪梅,柯红林.海马与糖尿病认知功能障碍[J].神经解剖学杂志,2004,20(6):637-640. 被引量:9
  • 3Wu Y,Li H,Loos RJ. Common variants in CDKALl,CDKN2A/B,IGF2BP2,SLC30A8,and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population[J].{H}DIABETES,2008,(10):2834-2842.
  • 4Hardy J,Singleton A. Genomewide association studies and human disease[J].{H}New England Journal of Medicine,2009,(17):1759-1768.
  • 5Palmer ND,Heste JM,An SS. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNPrs 7903146 is the causal diabetes susceptibility variant[J].{H}DIABETES,2011,(02):662-668.
  • 6Pinney SE,Simmons RA. Epigenetic mechanisms in the development of type 2 diabetes[J].{H}Trends in Endocrinology & Metabolism,2010,(04):223-229.
  • 7温洪波,张振馨,牛富生,李凌.北京地区蒙特利尔认知量表的应用研究[J].中华内科杂志,2008,47(1):36-39. 被引量:353
  • 8Sladek R, Rocheleau G, Rung J, et al. A genome- wide association study identifies novel risk loci for type 2 diabetes[J]. Nature, 2007,445(7130) :881-885.
  • 9Groves C J, Zeggini E, Minton J, et al. Association a- nalysis of 6,736 UK subjects provides replication and confirms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk [ J ]. Diabetes, 2006,55 (9) :2640-2644.
  • 10Weedon MN, McCarthy MI, Hitman G, et al. Combi- ning information from common type 2 diabetes risk pol- ymorphisms improves disease prediction [ J ]. PLoS Med, 2006,3 (10) : e374.

引证文献9

二级引证文献39

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