ACE基因I/D多态性与异常体液型2型糖尿病的关联研究
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  • 英文篇名:Study of Insertion / Deletion( I / D) Polymorphism in ACE Gene and Susceptibility to Type 2 Diabetes with Abnormal Hilit
  • 作者:吐尔逊·买买提 ; 茹柯耶·图尔贡 ; 吴志丹 ; 哈木拉提·吾甫尔 ; 宋曼殳 ; 多力坤·买买提玉素甫
  • 英文作者:Tursun·Mamat;Rukiya·Turgun;WU Zhi-dan;Hamulati·Wupuer;SONG Man-shu;Dolkun·Maitiyusup;College of the Life Sciences and Technology,Xinjiang University;Department of Medicine,Aksu Vocational and Technical College;No. 1 Middle School of Zham;Department of Uyghur Medicine,Xinjiang Medical University;School of Public Health and Family Medicine,Capital Medical University;
  • 关键词:异常体液性 ; 2型糖尿病 ; ACE基因 ; 多态性 ; 新疆汉族
  • 英文关键词:Abnormal Hilit;;Type 2 diabetes;;ACE gene;;Polymorphism;;Xinjiang Han population
  • 中文刊名:SWJS
  • 英文刊名:Biotechnology
  • 机构:新疆大学生命科学与技术学院;新疆阿克苏职业技术学院医学系;新疆温宿县佳木镇第一中学;新疆医科大学维吾尔医药系;首都医科大学公共卫生与家庭医学学院;
  • 出版日期:2014-10-15
  • 出版单位:生物技术
  • 年:2014
  • 期:v.24;No.144
  • 基金:国家自然科学基金项目(No.31460285);国家自然科学基金-青年科学基金项目(No.30901238);; 新疆维吾尔自治区科技支疆项目(No.201191247);; 新疆地方病分子生物学重点实验室开放基金项目(No.XJDX0208-2009-05)资助
  • 语种:中文;
  • 页:SWJS201405021
  • 页数:4
  • CN:05
  • ISSN:23-1319/Q
  • 分类号:87-90
摘要
目的:探讨血管紧张素转换酶(ACE)基因16内含子插入/缺失(I/D)多态性与新疆维吾尔自治区汉族人群异常体液型2型糖尿病(type 2 diabetes mellitus,T2DM)的关系。方法:用维吾尔医学和分子生物学技术互相结合的方法,分析87例T2DM患者和157例正常人ACE基因16内含子I/D多态性。结果:(1)异常粘液质型T2DM组II基因型的频率较对照组显著增高(20.00%比4.43%,p=0.023<0.05)。(2)在异常粘液质型T2DM组中携带ID、DD基因型的个体较携带II基因型的个体患T2DM的危险性增加(OR=5.618,95%CI为1.451-21.739;OR=4.386,95%CI为0.785-24.390)。结论:ACE基因16内含子插入/缺失(I/D)多态性与新疆汉族人异常粘液质型T2DM的危险性相关,与新疆汉族人异常胆液质型、异常黑胆质型和异常血液质型T2DM的危险性无关。
        Objective: To study the I / D polymorphism of ACE gene and it's susceptibility to type 2 diabetes( T2DM) in chinese Han population of Xinjiang. Method: Using the combined methods of Uighur medicine theory and molecular biology techniques to detect the I / D polymorphism at the intron 16 of the ACE gene in 87 T2 DM patients and 157 controls. Result:( 1) The frequency of the Ⅱ genotype for patients with abnormal Balgham Hilit was significantly higher than these for controls( 20. 00% vs 4. 43%,p = 0. 023 < 0. 05).( 2) Compared with II genotype,the susceptibility to T2 DM with the ID,DD genotypes were increased by 5. 618( OR = 5. 618,95% CI 为 1. 451-21. 739) and 4. 386( OR = 4. 386,95% CI 为 0. 785- 24. 390) in T2 DM patients with abnormal Balgham Hilit. Conclusion: These data suggest that the polymorphism of I / D of ACE gene have a susceptibility to T2 DM risk in patients of chinese Han population which carried with abnormal Balgham Hilit,and it is not associated with T2 DM risk in patients with uighur medicine abnormal Savda Hilit,uighur medicine abnormal Sapra Hilit and uighur medicine abnormal Qan Hilit.
引文
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