期刊文献+

亚洲人群FTO-rs9939609多态性与T2DM相关性分析

Analysis of the Association Between FTO-rs9939609 Polymorphism and Type 2 Diabetes in Asian Population
下载PDF
导出
摘要 目的探讨亚洲人群FTO基因rs9939609T> A多态性与2型糖尿病(T2DM)的相关性。方法通过检索Pubmed、EMbase、CNKI、万方数等据库,查找关于FTO基因与T2DM相关性的病例对照研究,检索时限为2010年1月-2018年11月。对文献的质量进行评价和资料提取,利用State12.0软件合并OR值及95%可信区间(CI),评估符合质量标准文献FTO基因rs9939609 T> A多态性与2型糖尿病(T2DM)的相关性。结果共纳入文献8篇,累计样本量7 768例(T2DM病组3 867例,对照组3 901例)。Meta分析结果显示亚洲地区人群FTO基因rs9939609 AA型与2型糖尿病相关(OR=1.25,95%CI:1.16~1.34)。进一步对病例亚分组,东亚及中国地区人群rs9939609 AA型与T2DM同样具有相关性(东亚:OR=1.26,95%CI:1.13~1.38;中国:OR=1.29,95%CI:1.13~1.45);而南亚地区合并OR=1.16,95%CI:0.83~1.48,不具有相关性。发表偏倚评估显示无发表偏倚。结论亚洲人群中FTO基因rs9939609 AA型与2型糖尿病具有相关性,增加了T2DM的发病风险。 Objective To investigate the association between FTO gene rs9939609 t > A polymorphism and type 2 diabetes mellitus(T2 DM) in Asian population.Methods Through searching PubMed,EMBASE,CNKI,Wanfang and other databases,we can find the case-control study on the correlation between FTO gene and T2 DM,and the retrieval time limit is from January 2010 to November 2018.To evaluate the quality of the literature and extract the data,using state12.0 software combined with or value and 95% confidence interval(CI),to evaluate the association between the polymorphism of FTO gene rs9939609 T > A and type 2 diabetes mellitus(T2 DM).Results The total number of samples was 7 768(3 867 in T2 DM group and 3 901 in control group).Meta analysis showed that the FTO gene rs9939609 AA was associated with type 2 diabetes mellitus(OR = 1.25,95% CI:1.16 ~ 1.34).Further to the case subgroups,there was also a correlation between rs9939609 AA and T2 DM in East Asia and China(East Asia:OR = 1.26,95% CI:1.13 ~ 1.38;China:OR = 1.29,95% CI:1.13 ~ 1.45).However,there was no correlation between OR = 1.16 and 95% CI:0.83 ~ 1.48 in South Asia.The publication bias assessment showed no publication bias.Conclusion The FTO gene rs9939609 AA is associated with type 2 diabetes in Asian population,which increases the risk of T2 DM.
作者 刘颖娟 杨钢 杨桂 LIU Yingjuan;YANG Gang;YANG Gui(Department of Clinical Laboratory,Zhongnan Hospital of Wuhan University,Wuhan Hubei 430071,China)
出处 《中国继续医学教育》 2019年第35期116-118,共3页 China Continuing Medical Education
关键词 FTO基因 单核苷酸多态性 2型糖尿病 亚洲人群 META分析 rs9939609 AA型 fat mass and obesity-associated gene(FTO) SNP type 2 diabetes mellitus Asian population Meta analysis rs9939609 AA
  • 相关文献

参考文献5

二级参考文献32

  • 1韩素萍.老年妇科肿瘤的诊治特点[J].实用老年医学,2006,20(6):365-367. 被引量:12
  • 2刘新民.妇产科手术学[M].3版.北京:人民卫生出版社,2010:906-907.
  • 3Xi B, Zhang M, Wang C, et al. The common SNP (rs9939609) in the FTO gene modifies the association be- tween obesity and high blood pressure in Chinese children. Mol Biol Rep, 2013, 40 : 773 -778.
  • 4Lucky M H, Baig S, Zil-e-Rubab H D, et al. Association of rs9939609 FTO gene variant with obesity among Karachi ad- olescent. Eur J Biotech Biosci,2014, 2 : 20 ~ 24.
  • 5de Luis DA, Aller R, Conde R, et al. The rs9939609 gene variant in FTO modified the metabolic response of weight loss after a 3-month intervention with a hypocaloric diet. J Invest Med, 2013, 61 : 22-26.
  • 6Kalnina I, Zabarenko L, Vaivade I, et al. Polymorphisms in FFO and near TMEM18 associate with type 2 diabetes and predispose to younger age at diagnosis of diabetes. Gene, 2013, 527 : 462 ~468.
  • 7Alosco M L, Benitez A, Gunstad J, et al. Reduced memory in fat mass and obesity - associated allele carriers among ol- der adults with cardiovascular disease. Psychogeriatrics, 2013, 13:35-40.
  • 8Lunnon K, Mill J. Epigenetic studies in Alzheimer's dis- ease: current findings, caveats, and considerations for fu- ture studies. Am J Med Genet B, 2013, 162 : 789 ~799.
  • 9Soloway AH, Soloway PD, Warner VD. Possible chemicalinitiators of cognitive dysfunction in phenylketonuria, Par- kinson's disease and Alzheimer's disease. Med Hypotheses, 2013, 81 : 690 - 694.
  • 10Chung SJ, Kim SY, Kim J, et al. Distinct genetic variants in Alzheimer~ disease and type 2 diabetes (P2. 149). Neu- rology, 2014, 82(10 Supplement) : 149.

共引文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部