首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >The homocysteine associated variant rs548987 of SLC17A3 confers susceptibility to ischemic stroke in Chinese population
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The homocysteine associated variant rs548987 of SLC17A3 confers susceptibility to ischemic stroke in Chinese population

机译:SLC17A3的同型半胱氨酸相关变体rs548987使中国人群易患缺血性中风

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摘要

Ischemic stroke is a common cause of death due to obstructed blood supply of the brain. Despite growing numbers of research, etiology underlying ischemic stroke remains complex and elusive. Elevated plasma homocysteine has been known as a risk factor for ischemic stroke. Recently, a genome-wide association study reported association between rs548987 of SLC17A3 and homocysteine. Given existing relation between homocysteine and ischemic stroke, SLC17A3 was believed to be a promising candidate gene of ischemic stroke. Indeed, its association with ischemic stroke was previously reported in a western population. Herein, we used rs548987 as a candidate genetic variant of ischemic stroke and performed association analysis in a Chinese population with 918 ischemic stroke cases and 979 controls. Although rs548987 failed to show significant association with total ischemic stroke and large vessel disease subtype, the C allele of rs548987 showed significant association with small vessel disease subtype of ischemic stroke (OR = 0.68, p = 0.004). Our preliminary results suggested different genetic etiology underlying the two most common subtypes of ischemic stroke and provided additional evidence to understand contribution of homocysteine to the disease. (C) 2016 Elsevier B.V. All rights reserved.
机译:缺血性中风是由于大脑供血受阻而导致的常见死亡原因。尽管有越来越多的研究,但缺血性中风的病因学仍然复杂而难以捉摸。血浆高半胱氨酸水平升高是缺血性卒中的危险因素。最近,全基因组关联研究报告了SLC17A3的rs548987与高半胱氨酸之间的关联。鉴于同型半胱氨酸与缺血性中风之间存在现有的关系,SLC17A3被认为是缺血性中风的有前途的候选基因。的确,它与缺血性中风的关联先前在西方人群中已有报道。在这里,我们使用rs548987作为缺血性中风的候选遗传变异体,并在918名缺血性中风病例和979例对照的中国人群中进行了关联分析。尽管rs548987未能显示出与总缺血性卒中和大血管疾病亚型的显着相关性,但rs548987的C等位基因显示出了与缺血性卒中的小血管疾病亚型的显着相关性(OR = 0.68,p = 0.004)。我们的初步结果表明,缺血性中风的两种最常见亚型具有不同的遗传病因,并为了解高半胱氨酸对疾病的贡献提供了额外的证据。 (C)2016 Elsevier B.V.保留所有权利。

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