文章摘要
李晓晶1 苏燕1△ 闫朝丽2△ 张晶晶1 顾丽1 秦文斌1 李彩萍2 李爱珍2 赵静3.SLC30A8 基因rsl3266634 多态性与内蒙古地区汉族人群2 型糖尿 病的相关性研究[J].,2011,11(12):2221-2223
SLC30A8 基因rsl3266634 多态性与内蒙古地区汉族人群2 型糖尿 病的相关性研究
Association of rs13266634 Polymorphism in SLC30A8 Gene with Type 2Diabetes in Han Population of Inner Mongolia
  
DOI:
中文关键词: 单核苷酸多态性  SLC30A8 基因  2 型糖尿病
英文关键词: Single Nucleotide Polymorphism  SLC30A8 gene  Type 2 Diabetes
基金项目: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) 和秦文斌科技助研基金项目(200911)的资助
作者单位
李晓晶1 苏燕1△ 闫朝丽2△ 张晶晶1 顾丽1 秦文斌1 李彩萍2 李爱珍2 赵静3 包头医学院生物化学与分子生物学教研室 
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中文摘要:
      目的:研究内蒙古地区汉族人群SLC30A8 (solute carrier family 30, member 8) 基因rsl3266634 单核苷酸多态性(Single nucleotide polymorphism, SNP)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 特异性聚合酶链式反应(AS-PCR),对222 例内蒙古地区汉族人(其中T2DM 组125 例,正常对照NC 组97 例)rsl3266634 进行基 因分型。结果:T2DM 组中rsl3266634 的C 等位基因频率、CC 基因型频率分别为61.2%和28.4%,均显著高于NC 组的53.1%和 24.7%(P 值均<0.05);而T2DM 组的TT 基因型频率为6.4%,显著低于NC 组的18.6%(P<0.05)。C 等位基因携带者患T2DM 的 风险是T 等位基因的1.64 倍(OR=1.64, 95%CI=1.125-2.402)。结论:SLC30A8 基因rsl3266634 多态性位点的C 等位基因可能是 T2DM 的风险等位基因,该位点C/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。
英文摘要:
      Objective: To study association of alleles and genotype frequencies of rsl3266634 single nucleotide polymorphism in SLC30A8 (solute carrier family 30, member 8) gene with type 2 diabetes mellitus in Han population of Inner Mongolia. Methods: Using allele-specific polymerase chain reaction, the rsl3266634 polymorphism of SLC30A8 gene was genotyped in 222 Han population of Inner Mongolia, including 125 patients with type 2 diabetes (T2DM group) and 97 normal controls (NC group). Results: In T2DM group, the frequencies of C allele and CC genotype of rsl3266634 were 61.2% and 28.4% respectively, they were significantly higher than those (53.1% and 24.7%) in the NC group (P<0.05); The TT genotype was significantly lower than that of the NC group (P<0.05). The risk of T2DM was significantly increased by C allele with T allelic odd ratio(OR) of 1.64 (OR=1.64, 95% CI=1.125-2.402). Conclusion: C allele of rsl32666634 polymorphism site in SLC30A8 gene might be a risk factor of T2DM, the site C/T polymorphism is associated with Type 2 diabetes and SLC30A8 gene might be a susceptible gene of T2DM in Han population of Inner Mongolia.
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