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在中国汉族人群中,NINJ2 基因内 12p13 位点 rs11833579 和 rs12425791 单核苷酸多态性与缺血性脑卒中无关。

No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population.

机构信息

The Institute of Hypertension and Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Atherosclerosis. 2011 Jun;216(2):381-2. doi: 10.1016/j.atherosclerosis.2011.02.005. Epub 2011 Mar 3.

Abstract

Recent genome-wide association (GWA) studies have identified two intergenic single nucleotide polymorphisms (SNPs) (rs11833579 and rs12425791) on chromosome 12p13 and within 11 kb of the NINJ2 gene that were significantly associated with stroke in Caucasians. However, the validity of the association has remained controversial. We performed genetic association analyses in three independent cohorts, including total of 3042 cases and 2973 controls. No significant association between these two SNPs and ischemic stroke was detected by meta-analysis after adjustment for cardiovascular risk factors under the additive model. Our data does not support that the common variants on 12p13 are major contributors of ischemic stroke in the Chinese Han population.

摘要

最近的全基因组关联 (GWA) 研究已经确定了两个位于染色体 12p13 上和 NINJ2 基因内 11kb 范围内的基因间单核苷酸多态性 (SNP) (rs11833579 和 rs12425791),它们与高加索人群中的中风显著相关。然而,这种关联的有效性一直存在争议。我们在三个独立的队列中进行了遗传关联分析,包括 3042 例病例和 2973 例对照。在加性模型下调整心血管危险因素后,通过荟萃分析未发现这两个 SNP 与缺血性中风之间存在显著关联。我们的数据不支持 12p13 上的常见变异是中国汉族人群缺血性中风的主要贡献因素。

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