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RNF213 p.R4810K 变异在伴有颅内动脉狭窄的早发性卒中中的流行率。

Prevalence of RNF213 p.R4810K Variant in Early-Onset Stroke With Intracranial Arterial Stenosis.

机构信息

From the Department of Neurology (T.K., S.O., T.Y., M.I.), National Cerebral and Cardiovascular Center, Osaka, Japan.

Department of Neurology, Osaka University Graduate School of Medicine, Japan (S.O.).

出版信息

Stroke. 2019 Jun;50(6):1561-1563. doi: 10.1161/STROKEAHA.118.024712. Epub 2019 May 7.

Abstract

Background and Purpose- The ring finger protein 213 gene ( RNF213) is a susceptibility gene for moyamoya disease and large-artery ischemic stroke in East Asia. We examined the prevalence and correlates of the RNF213 p.R4810K variant in patients with early-onset ischemic stroke in a Japanese single-center cohort. Methods- We analyzed 70 early-onset stroke patients with intracranial arterial stenosis who developed a noncardioembolic stroke or transient ischemic attack from 20 to 60 years of age. Patients with moyamoya disease were excluded. Results- The RNF213 p.R4810K variant was found in 17 patients (24%), and more often in women than men (38% versus 16%, odds ratio 3.3; 95% CI, 1.1-10.2, P=0.04). The variant was identified in 35% of patients with stenosis in the M1 segment of the middle cerebral artery or the A1 segment of the anterior cerebral artery (odds ratio, 25.0; 95% CI, 1.4-438; P<0.01) but in only one patient (9%) with intracranial posterior circulation stenosis. Conventional atherosclerotic risk factors did not differ between variant carriers and noncarriers. Conclusions- The RNF213 p.R4810K variant is common in early-onset ischemic stroke with anterior circulation stenosis in Japan. Further investigation of the RNF213 gene will provide new insights into pathogenetic mechanisms of early-onset stroke.

摘要

背景与目的-环指蛋白 213 基因(RNF213)是东亚人群中导致烟雾病和大动脉粥样硬化性缺血性卒中的易感基因。本研究在日本单中心队列中,检测了早发性缺血性卒中患者中 RNF213 p.R4810K 变异的流行率及其相关因素。方法-我们分析了 70 名颅内动脉狭窄的早发性卒中患者,这些患者年龄在 20-60 岁之间,发生了非心源性脑卒中和短暂性脑缺血发作。排除了烟雾病患者。结果-RNF213 p.R4810K 变异在 17 名患者(24%)中发现,且女性多于男性(38%比 16%,优势比 3.3;95%置信区间,1.1-10.2,P=0.04)。该变异在大脑中动脉 M1 段或大脑前动脉 A1 段狭窄的患者中占 35%(优势比,25.0;95%置信区间,1.4-438;P<0.01),而在颅内后循环狭窄的患者中仅占 1 例(9%)。变异携带者和非携带者的传统动脉粥样硬化危险因素无差异。结论-RNF213 p.R4810K 变异在日本早发性前循环狭窄性缺血性卒中患者中较为常见。对 RNF213 基因的进一步研究将为早发性卒中的发病机制提供新的见解。

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