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中国上海地区汉族人PGC-1α基因多态性与2型糖尿病相关性研究
引用本文:王艳波,于永春,李智,汪纯,王吉影,吴国亭.中国上海地区汉族人PGC-1α基因多态性与2型糖尿病相关性研究[J].中华医学遗传学杂志,2005,22(4):453-456.
作者姓名:王艳波  于永春  李智  汪纯  王吉影  吴国亭
作者单位:1. 200072,上海,同济大学附属第十人民医院中心实验室
2. 200072,上海,同济大学附属第十人民医院内分泌科
基金项目:国家自然科学基金(30270632)
摘    要:目的 研究过氧化物酶增殖激活受体-γ共激活子-1α(peroxisome proliferators-activated reeeptor-γ coactivator-1α,PGC-1α)基因单核苷酸多态性(single nucleotide polymorphism,SNP)与2型糖尿病(type 2 diabetes mellitus,T2DM)的关联性。方法 应用聚合酶链反应-限制性内切酶片段长度多态性技术,选择PGC-1α基因4个常见SNPs位点:Thr394Thr(ACG→ACA)、Gly482Ser(GGT→AGT)、Thr612Met(ACG→ATG)和IVS2+52C→A,对69个T2DM家系(310例)进行基因分型,并用传递不平衡检验(transmission-disequilibrium test,TDT)和同胞传递不平衡检验(sib transmission.disequilibrium,STDT)进行分析。用同样方法在无家族史的156例T2DM患者及111名糖耐量正常者中进行病例-对照关联分析,检验Gly482Ser多态性在散发人群中的分布。结果 (1)经TDT-STDT检验,未发现单个PGC-1α基因SNPs位点在T2DM患病子代中优势传递;(2)在病例-对照关联分析中,Gly482Ser位点多态性在两组人群的分布差异有统计学意义,携带者GA基因型罹患T2DM的危险性可增加1.85倍,且等位基因在两组人群的分布差异有统计学意义(P=0.046);(3)在无家族史的糖耐量正常者中,Gly482Ser位点的GG基因型的高密度脂蛋白胆固醇、低密度脂蛋白胆固醇和甘油三酯水平与GA+AA基因型比较,差异有统计学意义(分别为P=0.043,P=0.046,P=0.037)。结论 PGC-1α基因Gly482Ser多态性可能与T2DM的易感性相关。

关 键 词:中国  上海  汉族  PGC-1α基因  基因多态性  2型糖尿病  基因型
收稿时间:2004-09-08
修稿时间:2004年11月16

Study on the relationship between polymorphisms of peroxisome proliferators-activated receptor-γ coactivator-1α gene and type 2 diabetes in Shanghai Hans in China
WANG Yan-bo,YU Yong-Chun,LI Zhi,WANG Chun,WANG Ji-ying,WU Guo-ting.Study on the relationship between polymorphisms of peroxisome proliferators-activated receptor-γ coactivator-1α gene and type 2 diabetes in Shanghai Hans in China[J].Chinese Journal of Medical Genetics,2005,22(4):453-456.
Authors:WANG Yan-bo  YU Yong-Chun  LI Zhi  WANG Chun  WANG Ji-ying  WU Guo-ting
Institution:Department of Medical Laboratory, the Tenth People Hospital, Tongji University, Shanghai, 200072 PR China.
Abstract:OBJECTIVE: To observe the association between single nucleotide polymorphism (SNP) of peroxisome proliferators-activated receptor-gamma coactivator-1alpha (PGC-1alpha ) gene and type 2 diabetes mellitus(T2DM). METHODS: Four common SNPs of PGC-1alpha gene were genotyped with polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) and then analyzed with transmission-disequilibrium test (TDT) and sib transmission-disequilibrium test (STDT) in 69 T2DM pedigrees (310 individuals). Furthermore, the authors performed a case-control study to genotype Gly482Ser in 156 patients with T2DM and 111 normal glucose tolerance people without family history. RESULTS: (1)There were no positive results in four variances in TDT-STDT analysis(P> 0.05). (2)The Gly482Ser exhibited a significant difference between the two groups. GA genotype carriers were at increased risk for T2DM (OR=1.85), and there was statistically significant difference in the allele frequency between the case and control groups(P=0.046). (3) The subjects with GG genotype at position Gly482Ser had a higher HDL-C and lower LDL-C and TG levels when compared against those with GA+AA genotype in the control group without family history(P=0.043,lzP=0.046, P=0.037 respectively). CONCLUSION: This study suggested that the PGC-1alpha gene might be implicated in the pathogenesis of T2DM. But the studied SNPs in PGC-1alpha gene may not be major susceptibility ones of T2DM mellitus in Han people of Shanghai.
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