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东亚人群中9号染色体短臂21区遗传变异与冠心病风险的关联:一项荟萃分析。

Association of chromosome 9p21 genetic variants with risk of coronary heart disease in the East Asian population: a meta-analysis.

作者信息

Dong Liping, Wang Haoran, Wang Dao Wen, Ding Hu

机构信息

Department of Nephrology Puai Hospital Tongji Medical College, Huazhong University of Science & Technology, Wuhan, People's Republic of China.

出版信息

Ann Hum Genet. 2013 May;77(3):183-90. doi: 10.1111/ahg.12010. Epub 2013 Jan 24.

DOI:10.1111/ahg.12010
PMID:23347249
Abstract

Our aim was to evaluate the effect of SNPs in the 9p21 locus on genetic susceptibility of coronary heart disease in the East Asian population. We searched PubMed, EMBASE and CNKI for publications relating to the association between SNPs within the 9p21 locus and coronary heart disease in the East Asian population. This meta-analysis was assessed by STATA 9.2. Twenty-one studies from 15 eligible papers composing 25,945 cases and 31,777 control subjects were included in the meta-analysis. The odds ratio (OR) and 95% confidence interval (CI) for the risk allele was 1.30 (1.25-1.35) with moderate heterogeneity. No publication bias was observed in this study. Sensitivity analysis further strengthened the validity of this association. In conclusion, SNPs within the 9p21 locus were strongly associated with the risk of coronary heart disease in the East Asian population with a similar risk OR to the Caucasian population.

摘要

我们的目的是评估9p21基因座中的单核苷酸多态性(SNPs)对东亚人群冠心病遗传易感性的影响。我们在PubMed、EMBASE和中国知网中检索了与东亚人群9p21基因座内SNPs与冠心病关联相关的文献。本荟萃分析采用STATA 9.2进行评估。荟萃分析纳入了15篇合格论文中的21项研究,共25945例病例和31777例对照。风险等位基因的比值比(OR)和95%置信区间(CI)为1.30(1.25 - 1.35),存在中度异质性。本研究未观察到发表偏倚。敏感性分析进一步加强了这种关联的有效性。总之,9p21基因座内的SNPs与东亚人群冠心病风险密切相关,其风险OR与白种人群相似。

相似文献

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Association of chromosome 9p21 genetic variants with risk of coronary heart disease in the East Asian population: a meta-analysis.东亚人群中9号染色体短臂21区遗传变异与冠心病风险的关联:一项荟萃分析。
Ann Hum Genet. 2013 May;77(3):183-90. doi: 10.1111/ahg.12010. Epub 2013 Jan 24.
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引用本文的文献

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Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity?在遗传生物银行时代,人口结构是否无关紧要、是一个挑战还是一个机会?
Hum Genet. 2020 Jan;139(1):23-41. doi: 10.1007/s00439-019-02014-8. Epub 2019 Apr 27.
2
Genetic variation in 9p21 is associated with fasting insulin in women but not men.9p21 上的遗传变异与女性而非男性的空腹胰岛素有关。
PLoS One. 2018 Aug 23;13(8):e0202365. doi: 10.1371/journal.pone.0202365. eCollection 2018.
3
Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association.
《2017年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2017 Mar 7;135(10):e146-e603. doi: 10.1161/CIR.0000000000000485. Epub 2017 Jan 25.
4
Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary Lesions: An Observational Study.9号染色体p21多态性对无冠状动脉病变的汉族人群心血管死亡率预测的价值:一项观察性研究。
Medicine (Baltimore). 2015 Sep;94(39):e1538. doi: 10.1097/MD.0000000000001538.
5
Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.验证了 9p21 区域内的基因变异与冠心病风险的上下文相关关联:社区动脉粥样硬化风险研究。
Hum Genet. 2014 Sep;133(9):1105-16. doi: 10.1007/s00439-014-1451-3. Epub 2014 Jun 3.