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[脑血管疾病的分子流行病学;久山研究与福冈卒中登记(FSR)]

[Molecular epidemiology of cerebrovascular diseases; the Hisayama study and the Fukuoka Stroke Registry (FSR)].

作者信息

Kitazono Takanari, Kubo Michiaki, Hata Jun, Ibayashi Setsuro, Kiyohara Yutaka, Iida Mitsuo

机构信息

Department of Nephrology, Hypertension, and Strokology, Kyushu University Hospital.

出版信息

Rinsho Shinkeigaku. 2008 Nov;48(11):892-5. doi: 10.5692/clinicalneurol.48.892.

Abstract

The underlying pathogenesis of stroke is mediated by a variety of environmental risk factors as well as genetic ones. Thus, we have to evaluate the environmental factors precisely to identify the stroke-related gene polymorphisms. The Hisayama study, an epidemiological study of cardiovascular diseases, was established in 1961 in Hisayama, Japan. In 2002, a screening survey for the genetic study was performed in Hisayama. The Fukuoka Stroke Registry (FSR) is a hospital-based registration of stroke patients. Stroke specialists from eight medical centers in southern Japan have participated in FSR. In the present study, control and case subjects were recruited from the Hisayama study and FSR, respectively. We performed a genome-wide case-control study and found that a nonsynonymous SNP in PRKCH encoding a member of protein kinase C (PKCC eta) was significantly associated with brain infarction. As a candidate gene analysis, we investigated the role of NAD (P) H oxidase C242T polymorphism in the development of brain infarction. The C242T polymorphism was not associated with lacunar and atherothrombotic infarction; however, the presence of T-allele may have a protective role in the occurrence of atrial fibrillation and cardioembolic brain infarction. These studies may provide important information for the development of the therapeutic strategies against stroke.

摘要

中风的潜在发病机制是由多种环境风险因素以及遗传因素介导的。因此,我们必须精确评估环境因素以识别与中风相关的基因多态性。久山研究是一项关于心血管疾病的流行病学研究,于1961年在日本久山建立。2002年,在久山进行了一项用于基因研究的筛查调查。福冈中风登记处(FSR)是一个基于医院的中风患者登记处。日本南部八个医疗中心的中风专家参与了FSR。在本研究中,对照和病例受试者分别从久山研究和FSR中招募。我们进行了一项全基因组病例对照研究,发现编码蛋白激酶C(PKCC eta)成员的PRKCH中的一个非同义单核苷酸多态性(SNP)与脑梗死显著相关。作为一项候选基因分析,我们研究了NAD(P)H氧化酶C242T多态性在脑梗死发生中的作用。C242T多态性与腔隙性梗死和动脉粥样硬化血栓形成性梗死无关;然而,T等位基因的存在可能对心房颤动和心源性脑梗死的发生具有保护作用。这些研究可能为制定中风治疗策略提供重要信息。

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