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TCF7L2基因rs7903146和rs11196218单核苷酸多态性与新诊断2型糖尿病患者早相胰岛素分泌的相关性分析 被引量:10

Correlation between single nucleotide polymorphisms of rs7903146 and rs11196218 at TCF7L2 gene and the early phase insulin secretion of newly diagnosed patients with type 2 diabetes
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摘要 目的探讨重庆地区汉族人群中转录因子7类似物2(TCF7L2)基因rs7903146和rs11196218单核苷酸多态性(SNPs)与新诊断2型糖尿病(T2DM)早相胰岛素分泌的相关性。方法采用病例-对照研究方法,设新诊T2DM组(n=227)和正常对照组(n=152),采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)技术对rs7903146和rs11196218位点进行SNPs分型。结果新诊T2DM组和正常对照组rs7903146位点风险等位基因频率(MAF)分别为5.73%和4.28%,二者间差异无统计学意义。Logistic回归无论以共显性、显性、或是隐性模式分析,rs7903146和rs11196218位点的SNPs均与T2DM无显著相关性(P>0.05)。Rs7903146位点的SNPs与ΔI30/ΔG30相关(OR=1.012,95%CI 1.000~1.025,P=0.05),T风险等位基因携带者的ΔI30/ΔG30显著高于未携带者(P=0.0385)。结论尚未发现重庆地区汉族人群TCF7L2基因rs7903146和rs11196218位点SNPs与T2DM的相关性,但rs7903146位点的基因多态性可能与早相胰岛素分泌有关。 Objective To investigate the correlation between single nucleotide polymorphisms(SNPs) of rs7903146 and rs11196218 at TCF7L2 gene and the early phase insulin secretion of newly diagnosed patients with type 2 diabetes mellitus(T2DM).Methods A case-control study was conducted in 227 newly diagnosed patients with T2DM(T2DM group) and 152 normal people(control group) from Chongqing area.SNPs of rs7903146 and rs11196218 were genotyped by matrix assisted laser desorption/ionization time-of-flight mass spectrometry(MALDI-TOF MS).Results The minor allele frequencies(MAF) of rs7903146 in T2DM and control group were 5.73% and 4.28%,respectively,with no significant difference.Logistic regression analysis revealed that the SNPs of rs7903146 and rs11196218 were negatively associated with T2DM no matter with additive,dominant or recessive models(P〉0.05).The SNPs of rs7903146 were associated with ΔI30/ΔG30(OR=1.012,95%CI 1.000-1.025,P=0.05),the levels of ΔI30/ΔG30 in T-allele carriers were significantly higher than that in normal allele carriers(P=0.0385).Conclusion There is no significant correlation between SNPs of rs7903146 and rs11196218 at TCF7L2 gene and newly diagnosed T2DM,but SNPs of rs7903146 may associate with the early phase insulin secretion.
出处 《解放军医学杂志》 CAS CSCD 北大核心 2011年第3期269-272,共4页 Medical Journal of Chinese People's Liberation Army
基金 重庆市卫生局医学科学研究基金(2008-2-96) 重庆医科大学附属第一医院医学科学基金(YXJJ2009-03)
关键词 糖尿病 2型 转录因子7类似物2 多态性 单核苷酸 diabetes mellitus, type 2 TCFTL2 polymorphism, single nucleotide
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  • 1Lewontin R. On measures of gametic disequilibrium. Genetics 1988; 120:849-52.
  • 2Chen WY, Shi YY, Zheng YL, et al. Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Hum Mol Genet 2004; 13:2991-5.
  • 3Shi Y, Zhao X, Yu L, et al. Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population. Genome Res 2004; 14:1345-9.
  • 4Zhao X, Shi Y, Tang J, et al. A case control and family based association study of the neuregulinl gene and schizophrenia. J Med Genet 2004; 41:31-4.
  • 5Guo S, Shi Y, Zhao X, et al. No genetic association between polymorphisms in the AMPA receptor subunit GluR4 gene (GRIA4) and schizophrenia in the Chinese population. Neurosci Lett 2004; 369:168-72.
  • 6Yang MS, Yu L, Guo TW, et al. Evidence for association between single nucleotide polymorphisms in T complex protein 1 gene and schizophrenia in the Chinese Han population. J Med Genet 2004; 41:e63.
  • 7Kejnovsky E;Kypr J.DNA extraction by zinc[J],1997.
  • 8Attal J;Cajero Juarez M;Houdebine LM.A simple method of DNA extraction from whole tissues and blood using glass powder for detection of transgenic animals by PCR[J],1995(2).
  • 9赵书平,张俊洁,尤建,杨玉红,郭峰.一种碘化钾提取外周血基因组DNA的方法[J].中华医学遗传学杂志,1999,16(6):395-396. 被引量:57
  • 10刘巧红,滕云,沈凌汛.HLA-DR抗原β链的共同表位与类风湿关节炎相关性研究[J].风湿病学杂志,2000,4(3):153-155. 被引量:14

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  • 1林大东,毕新岭,缪明永,顾军,朱克军,米庆胜.银屑病患者血浆血小板活化因子乙酰水解酶活性变化及其临床意义[J].中国皮肤性病学杂志,2004,18(7):387-388. 被引量:6
  • 2陈秋,夏永鹏,邱宗荫.胰岛素耐受的HepG2细胞模型建立[J].细胞生物学杂志,2005,27(3):334-338. 被引量:23
  • 3夏天保,顾军,毕新岭,臧远胜,王洁,孙清菊.血小板活化因子乙酰水解酶基因Ile198Thr突变与银屑病的相关研究[J].中国麻风皮肤病杂志,2006,22(1):17-19. 被引量:4
  • 4Stafforini DM, Satoh K, Atkinson DL, et al, Platelet-activating factor acetylhydrolase deficiency. A missense mutation near the active site of an anti-inflammatory phospholipase[J]. J Clin Invest, 1996, 97(12): 2784-2791.
  • 5Kruse S, Mao XOa Heinzmann A, et al. The Ile198Thr and Ala379Val variants of plasmatic paf-acetylhydrolase impair catalytical activities and are associated with atopy and asthma [J]. AmJ Hum Genet, 2000, 66(5): 1522-1530.
  • 6Taylor JG, Choi EH, Foster CB, et al. Using genetic variation to study human disease[J]. Trends Mol Med, 2001, 7(11): 507- 512.
  • 7Prescott SM, Zimmerman GA, Stafforini DM,et al. Plateletactivating factor and related lipid mediators[J]. Annu Rev Biochem, 2000, 69: 419-445.
  • 8Yamaguchi S, Tomomatsu N, Komatsu H. Effect of Y-24180, a receptor antagonist to platelet-activating factor (PAF), on allergic cutaneous reactions in actively sensitized mice[J]. Inflamm Res, 2000, 49 ( 11 ): 584-90.
  • 9Mallet AI, Cunningham FM. Structural identification of platelet activating factor in psoriatic scale[J]. Biochem Biophys Res Commun, 1985, 126 (1): 192-198.
  • 10Guerra R, Zhao B, Mooser V, et al. Determinants of plasma platelet-activating factor acetylhydrolase:heritability and relationship to plasma lipnproteins[J]. J Lipid Res, 1997, 38(11): 2281-2288.

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