A Reduced Interval of Chromosome 9p21 Locus is Associated with Ischemic Stroke in Chinese Northern Han Population

Shuo Li, Yu-ming Xu, Hong Zheng, E. Randell, Haijian Wang, J. Cui, G. Sun, G. Zhai, Fei-yu Han, Yagang Xie
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Abstract

The 9p21 locus, a strong risk locus for coronary arterial disease, has been also associated with other cardiovascular disease including ischemic stroke (IS) in Caucasians. However, the association between 9p21 locus and IS in Chinese Han population is still debatable because of ambiguous results reported previously. Genetic heterogeneity between Southern and Northern Chinese Han populations could be one of the reasons for this uncertainty. Four genetic variants selected from the three conjunctional LD blocks within the 44 kb candidate region on chromosome 9p21 were genotyped in 1,429 IS patients and 1,191 healthy controls from the Northern Chinese Han population. Among the four studied variants, the G allele of the SNP rs2383207 was significantly associated with IS with allele frequency 66.8% in patients and 63.4% in controls. This association appears to be dominant with an OR of 1.417 (p=0.003) for people with either GG or AG genotypes. We did not find any association for the other three SNPs (rs1333049, rs10757274, and rs10116277). Based our results, we conclude that the 9p21 locus is a susceptibility locus for IS in the Northern Chinese Han population; and the core risk region for IS is within an interval of less than 28kb.
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染色体9p21位点缩短间隔与中国北方汉族缺血性脑卒中相关
9p21基因座是冠状动脉疾病的高危基因座,也与白种人的缺血性中风(IS)等其他心血管疾病有关。然而,由于先前报道的结果不明确,9p21位点与中国汉族IS之间的关系仍然存在争议。中国南方和北方汉族人群之间的遗传异质性可能是造成这种不确定性的原因之一。从9p21染色体44 kb候选区域的三个连接LD块中选择了四个遗传变异,对来自中国北方汉族人群的1429名IS患者和1191名健康对照进行了基因分型。在所研究的4个变异中,SNP rs2383207的G等位基因与IS显著相关,其等位基因频率在患者中为66.8%,在对照组中为63.4%。对于GG或AG基因型的人来说,这种关联似乎是显性的,OR为1.417 (p=0.003)。我们没有发现其他三个snp (rs1333049, rs10757274和rs10116277)的关联。基于我们的研究结果,我们得出结论,9p21位点是中国北方汉族人群is的易感位点;IS的核心危险区在小于28kb的区间内。
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