Detailed phenotype of RNF213 p.R4810K variant identified by the Chinese patients with acute ischaemic stroke or transient ischaemic attack.

IF 4.4 1区 医学 Q1 CLINICAL NEUROLOGY
Hongyu Zhou, Jing Jing, Yuehua Pu, Wei Li, Xia Meng, Anxin Wang, Yingting Zuo, Zhe Xu, Qin Xu, Yue Suo, Hao Li, Yongjun Wang
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引用次数: 0

Abstract

Background and purpose: The ring finger protein 213 gene (RNF213) p.R4810K variant increased the risk of acute ischaemic stroke (AIS) attributable to intracranial arterial stenosis (ICAS) in the Japanese and Korean populations. In this study, we aimed to examine the prevalence of the RNF213 p.R4810K variant in Chinese patients with AIS or transient ischaemic attack and identify the phenotype of the carriers.

Methods: We analysed data from the Third China National Stroke Registry. All included participants were divided into two groups by carrier status of the p.R4810K variant. The aetiological classification was conducted according to the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria. The presence of ICAS and extracranial arterial stenosis (ECAS) was defined as 50%-99% stenosis or occlusion of any intracranial and extracranial artery. Logistic regression models and Cox regression models were used to evaluate the association of the p.R4810K variant with TOAST classification, stenosis phenotypes and clinical outcomes.

Results: A total of 10 381 patients were enrolled, among which 56 (0.5%) had the heterozygote GA genotype for p.R4810K. The variant carriers were younger (p=0.01), and more likely to suffer from peripheral vascular disease (p=0.04). The p.R4810K variant was associated with large-artery atherosclerosis (LAA) (adjusted OR=1.94, 95% CI 1.13 to 3.33), anterior circulation stenosis (adjusted OR=2.12, 95% CI 1.23 to 3.65) and ECAS (adjusted OR=2.29, 95% CI 1.16 to 4.51). Nevertheless, the p.R4810K variant was not associated with recurrence, poor functional outcome and mortality at 3 months and 1 year.

Conclusions: The RNF213 p.R4810K variant was associated with LAA, anterior circulation stenosis and ECAS in Chinese patients. Given the low carrying rate and only 1-year follow-up information, caution should be taken to interpret our findings in no statistically significant association between the p.R4810K variant and stroke prognosis in Chinese patients.

中国急性缺血性脑卒中或短暂性脑缺血发作患者发现的 RNF213 p.R4810K 变异的详细表型。
背景和目的:在日本和韩国人群中,环指蛋白 213 基因(RNF213)p.R4810K 变异增加了因颅内动脉狭窄(ICAS)导致急性缺血性卒中(AIS)的风险。在这项研究中,我们旨在检测 RNF213 p.R4810K 变体在中国 AIS 或短暂性脑缺血发作患者中的流行率,并确定携带者的表型:我们分析了第三届中国卒中登记中心的数据。方法:我们分析了第三届中国全国脑卒中登记中心的数据,按照p.R4810K变异体的携带状态将所有纳入者分为两组。根据急性卒中治疗中的 Org 10172 试验(TOAST)标准进行病因分类。ICAS和颅外动脉狭窄(ECAS)定义为任何颅内和颅外动脉50%-99%的狭窄或闭塞。采用逻辑回归模型和Cox回归模型评估p.R4810K变异与TOAST分类、狭窄表型和临床结果的关系:共有 10 381 名患者入选,其中 56 人(0.5%)具有 p.R4810K 杂合子 GA 基因型。变异携带者更年轻(p=0.01),更有可能罹患外周血管疾病(p=0.04)。p.R4810K变异与大动脉粥样硬化(LAA)(调整后OR=1.94,95% CI 1.13至3.33)、前循环狭窄(调整后OR=2.12,95% CI 1.23至3.65)和ECAS(调整后OR=2.29,95% CI 1.16至4.51)有关。然而,p.R4810K变异与3个月和1年后的复发、不良功能预后和死亡率无关:结论:RNF213 p.R4810K变异与中国患者的LAA、前循环狭窄和ECAS有关。由于携带率较低且仅有 1 年的随访资料,因此在解释我们的研究结果时应谨慎,即 p.R4810K 变异与中国患者的卒中预后无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Stroke and Vascular Neurology
Stroke and Vascular Neurology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
11.20
自引率
1.70%
发文量
63
审稿时长
15 weeks
期刊介绍: Stroke and Vascular Neurology (SVN) is the official journal of the Chinese Stroke Association. Supported by a team of renowned Editors, and fully Open Access, the journal encourages debate on controversial techniques, issues on health policy and social medicine.
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