Literature DB >> 20031605

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.

Hu Ding1, Yujun Xu, Xiaojing Wang, Qi Wang, Lan Zhang, Yuanchao Tu, Jiangtao Yan, Wei Wang, Rutai Hui, Cong-Yi Wang, Dao Wen Wang.   

Abstract

BACKGROUND: Recent studies on genome-wide association have identified common variants on chromosome 9p21 associated with coronary artery disease (CAD). Given that ischemic stroke and CAD share several aspects of etiology and pathogenesis, we investigated the association of variants on chromosome 9p21 with ischemic stroke and CAD in the Chinese Han population by capturing the majority of diversity in this locus using haplotype-tagging single-nucleotide polymorphisms. METHODS AND
RESULTS: We performed a shared control-cases study using 15 tagging single-nucleotide polymorphisms and 2 previously reported susceptibility single-nucleotide polymorphisms spanning 58 kb of the chromosome of 9p21 in a set of 558 patients with ischemic stroke, 510 patients with CAD, and 557 unaffected participants (controls) in the Chinese Han population. The association analyses were performed at both SNP and haplotype levels. We further verified our findings in an independent cohort of 442 ischemic stroke cases and 502 control subjects. In the first study, rs2383206, rs1004638, and rs10757278 in block 3 were significantly associated with CAD but not with ischemic stroke independent of traditional cardiovascular risk factors in additive model (P = 0.002 to 0.0001, q = 0.026 to 0.004). Analysis from all blocks revealed that haplotype profiles of block 3 on 9p21 were significantly different between shared control and cases of CAD (P = 1.3 x 10(-10), q = 1.2 x 10(-9)) and ischemic stroke (P = 1.7 x 10(-6), q = 7.7 x 10(-6)). In the expanded second case-control study, block 3 on 9p21 remained associated with ischemic stroke (P = 2.6 x 10(-4), q = 6.3 x 10(-4)).
CONCLUSIONS: Our results suggest for the first time that 9p21 is a shared susceptibility locus, strongly for CAD and weakly for ischemic stroke, in a Chinese Han population.

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Year:  2009        PMID: 20031605     DOI: 10.1161/CIRCGENETICS.108.810226

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN: 1942-3268


  37 in total

1.  Chromosome 9p21.3 Variants Are Associated with Cerebral Infarction in Chinese Population.

Authors:  Xuanye Yue; Lili Tian; Xinying Fan; Gelin Xu; Fu-Dong Shi; Xinfeng Liu
Journal:  J Mol Neurosci       Date:  2015-02-11       Impact factor: 3.444

2.  Chromosome 9p21 in ischemic stroke: population structure and meta-analysis.

Authors:  Christopher D Anderson; Alessandro Biffi; Natalia S Rost; Lynelle Cortellini; Karen L Furie; Jonathan Rosand
Journal:  Stroke       Date:  2010-04-15       Impact factor: 7.914

3.  Association between LGALS2 3279C>T and coronary artery disease: A case-control study and a meta-analysis.

Authors:  Jiangfang Lian; Peiliang Fang; Dongjun Dai; Yanna Ba; Xi Yang; Xiaoyan Huang; Junxin Li; Xiaoliang Chen; Jian Guo; Feng Guan; Ping Peng; Ruochi Zhao; Shangshi Zhang; Fang Gao; Linlin Tang; Cheng Zhang; Huihui Ji; Qingxiao Hong; Huadan Ye; Limin Xu; Qilong Zhong; Panpan Liu; Jianqing Zhou; Shiwei Duan
Journal:  Biomed Rep       Date:  2014-08-04

4.  The role of PRKCH gene variants in coronary artery disease in a Chinese population.

Authors:  Jun Zhu; Jian-Jun Yan; Zheng-Ping Kuai; Wei Gao; Jian-Jin Tang; En-Zhi Jia; Zhi-Jian Yang; Lian-Sheng Wang
Journal:  Mol Biol Rep       Date:  2011-05-29       Impact factor: 2.316

5.  Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.

Authors:  Nora Franceschini; Cara Carty; Petra Bůzková; Alex P Reiner; Tiana Garrett; Yi Lin; Jens-S Vöckler; Lucia A Hindorff; Shelley A Cole; Eric Boerwinkle; Dan-Yu Lin; Ebony Bookman; Lyle G Best; Jonathan N Bella; Charles Eaton; Philip Greenland; Nancy Jenny; Kari E North; Darin Taverna; Alicia M Young; Ewa Deelman; Charles Kooperberg; Bruce Psaty; Gerardo Heiss
Journal:  Circ Cardiovasc Genet       Date:  2011-10-31

Review 6.  Molecular genetics of coronary artery disease.

Authors:  Kouichi Ozaki; Toshihiro Tanaka
Journal:  J Hum Genet       Date:  2015-07-02       Impact factor: 3.172

7.  The combination of 9p21.3 genotype and biomarker profile improves a peripheral artery disease risk prediction model.

Authors:  Kelly P Downing; Kevin T Nead; Yoko Kojima; Themistocles Assimes; Lars Maegdefessel; Thomas Quertermous; John P Cooke; Nicholas J Leeper
Journal:  Vasc Med       Date:  2013-12-09       Impact factor: 3.239

8.  Genome-wide association study of coronary artery disease.

Authors:  Naomi Ogawa; Yasushi Imai; Hiroyuki Morita; Ryozo Nagai
Journal:  Int J Hypertens       Date:  2010-09-21       Impact factor: 2.420

9.  Association analysis of GWAS and candidate gene loci in a Chinese population with coronary heart disease.

Authors:  Min Gao; Haiqin Tang; Xiaodong Zheng; Fusheng Zhou; Wensheng Lu
Journal:  Int J Clin Exp Med       Date:  2015-05-15

Review 10.  Functional genomics of the 9p21.3 locus for atherosclerosis: clarity or confusion?

Authors:  Hsiao-Huei Chen; Naif A M Almontashiri; Darlène Antoine; Alexandre F R Stewart
Journal:  Curr Cardiol Rep       Date:  2014-07       Impact factor: 2.931

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