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IGF2BP2基因rs4402960多态性与内蒙古地区汉族人群2型糖尿病的相关性研究 被引量:1

Association of IGF2BP2 rs4402960 genotype with type 2 diabetes susceptibility in Han population living in Inner Mongolia region
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摘要 目的探讨内蒙古地区汉族人群胰岛素样生长因子2 mRNA结合蛋白(IGF2BP2)基因rs4402960单核苷酸多态性的等位基因和基因型频率分布与2型糖尿病(type 2 diabetes,T2DM)的相关性。方法采用等位基因特异性聚合酶链反应(AS-PCR)对360例内蒙古地区汉族人(T2DM组166例,正常对照组194例)rs4402960进行基因分型。结果 T2DM组中rs4402960的T等位基因频率和TT、GT基因型频率分别为41.6%、12.1%和59.0%,均高于正常对照组的10.6%、3.6%和13.9%(P均<0.05);而T2DM组的GG基因型频率为28.9%,低于正常对照组的82.5%(P<0.05)。携带T等位基因是患T2DM的危险因素(OR=6.02,95%CI=4.075~8.895)。结论 IGF2BP2基因rs4402960多态性位点的T等位基因可能是T2DM的风险等位基因,该位点G/T多态性与内蒙古地区汉族人群T2DM具有相关性,可能是内蒙古地区汉族人T2DM的易感基因之一。 Objective To study the association of alleles and genotype frequencies of rs4402960 in insulin-like growth factor 2 mRNA binding protein 2(IGF2BP2) gene with type 2 diabetes mellitus(T2DM) in Han population of Inner Mongolia region.Methods Allele-specific polymerase chain reaction was used to genotype the rs4402960 polymorphism of IGF2BP2 in 360 Han population living in the Inner Mongolia region,including 166 patients with T2DM(T2DM group) and 194 normal controls(NC group).Results The frequencies of T allele,TT and GT genotype of rs4402960 in T2 DM group were 41.6%,12.1% and 59.0%,respectively,which were significantly higher than those in the NC group(10.6%,3.6% and 13.9%,all P〈0.05).The GG genotype frequency was 28.9% in T2DM group,being significantly lower than that in the NC group(82.5%,P〈0.05).Carrying T allele was a risk factor of T2DM(OR = 6.02,95% CI = 4.075-8.895).Conclusion T allele of rs4402960 polymorphism in IGF2BP2 gene might be a risk factor of T2DM,and G/T polymorphism is associated with T2DM.IGF2BP2 rs4402960 might be a susceptible gene of T2DM in Han population living in Inner Mongolia region.
出处 《第二军医大学学报》 CAS CSCD 北大核心 2012年第8期915-917,共3页 Academic Journal of Second Military Medical University
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) 包头医学院秦文斌助研基金(200911)~~
关键词 2型糖尿病 单核苷酸多态性 IGF2BP2基因 type 2 diabetes single nucleotide polymorphism IGF2BP2 gene
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  • 1Zeggini E, Weeclon M N, Lindgren C M, Frayling T M, Elliott K S,Lango H, et al. Replication of genome-wide association sig- nals in UK samples reveals risk loci for type 2 diabetes[J]. Sci- ence, 2007,316 : 1336-1341.
  • 2Ng M C,Park K S,Oh B,Tam C H,Cho Y M,Shin H D,et al. Implication of genetic variants near TCFTL2, SLC30AS, HHEX,CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians[J].. Diabetes, 2008, 57; 2226-2233.
  • 3Omori S, Tanaka Y, Takahashi A, Hirose H, Kashiwagi A, Kaku K, et al. Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30AS, and KCNJ11 with susceptibility to type 2 di- abetes in a Japanese population[J]. Diabetes, 2008,57 : 791-795.
  • 4Hayashi T, Iwamoto Y, Kaku K, Hirose H, Maeda S. Replica- tion study for the association of TCF7L2 with susceptibility to type 2 diabetes in a Japanese population[J]. Diabetologia, 2007, 50 :980-984.
  • 5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
  • 6Spagnoli F M, Brivanlou A H. The RNA-binding protein VglRBP,is required for pancreatic fate specification[J]. Dev Bi ol, 2006,292: 442-456.
  • 7Frayling T M. Genome-wide association studies provide new in- sights into type 2 diabetes aetiology[J]. Nat Rev Genet, 2007, 8:657 -662.
  • 8Nielsen J, Christiansen J, Lykke-Andersen J, Johnsen A H, Wewer U M, Nielsen F C. A family of insulin-like growth factor l] mRNA binding proteins represses translation in late develop ment[J]. Mol Cell Biol, 1999,19 : 1262-1270.
  • 9Ruchat S M, Elks C E, Loos R J,Vohl M C, Weisnagel S J, Rankinen T,et al. Association between insulin secretion,insulin sensitivity and type 2 diabetes susceptibility variants identified in genome-wide association studies[J]. Acta Diabetol, 2009,46: 217-226.
  • 10Grarup N,Rose C S,Andersson E A,Andersen G,Nielsen A L, Albreehtsen A,et al. Studies of association of variants near the HHEX,CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: valida- tion and extension of genome-wide association studies[J]. Dia- betes,2007,56:3105-3111.

二级参考文献11

  • 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:3
  • 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.
  • 10邹万忠.肾活检病理诊断标准指导意见[J].中华肾脏病杂志,2001,17(4):270-274. 被引量:378

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