RNF213 p.Arg4810Lys变异与无症状颅内动脉狭窄进展较快有关。

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Shogo Dofuku, Satoru Miyawaki, Hideaki Imai, Masahiro Shimizu, Hiroki Hongo, Yuki Shinya, Kenta Ohara, Yu Teranishi, Hideaki Ono, Hirofumi Nakatomi, Akira Teraoka, Nobuhito Saito
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引用次数: 0

摘要

颅内动脉狭窄(ICAS)是缺血性中风的重要诱因之一,RNF213 p.Arg4810Lys 变异被认为是相关的遗传因素。我们探讨了无症状ICAS患者RNF213基因型的临床结果。2011年11月至2019年3月期间,139名无症状ICAS患者参与了这项研究。采用桑格测序法对 RNF213 p.Arg4810Lys 进行了基因分型。研究人员对 RNF213 基因型与背景特征以及同侧缺血性脑血管事件和狭窄进展等临床结果进行了综合分析比较。在25%的病例中发现了RNF213 p.Arg4810Lys,揭示了携带者和非携带者之间不同的临床特征。在平均 58 个月的随访期间,同侧缺血性脑血管事件的发生率为 4.3%(6/139 例),13%(18/139 例)的病例出现血管狭窄进展。RNF213变异组的狭窄进展率(25.7%;9/35 例)明显高于RNF213野生型组(8.7%;9/104 例)。RNF213 变异组的累积狭窄进展率明显高于 RNF213 野生型组(log-rank 检验,P = 0.0004)。多变量 Cox 回归分析表明,RNF213 p.Arg4810Lys 变异与狭窄进展风险增加之间存在明显关联(P = 0.03,几率比 3.2;95% 置信区间,1.1-9.0)。RNF213 p.Arg4810Lys变异在无症状的ICAS中表现出临床差异,并明显与狭窄进展风险增加有关。这些结果表明,与该变异体相关的血管狭窄机制存在明显差异,值得进一步研究其临床意义和潜在的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNF213 p.Arg4810Lys Variant Is Associated with Higher Stenosis Progression in Asymptomatic Intracranial Artery Stenosis.

Intracranial artery stenosis (ICAS) is a significant contributor to ischemic stroke, with the RNF213 p.Arg4810Lys variant identified as a related genetic factor. We explored the clinical outcomes of the RNF213 genotype in patients with asymptomatic ICAS. Between November 2011 and March 2019, 139 patients with asymptomatic ICAS were enrolled in this study. Genotyping for RNF213 p.Arg4810Lys was performed using Sanger sequencing. A comprehensive analysis was conducted to compare the RNF213 genotype with background characteristics and clinical outcomes such as ipsilateral ischemic cerebrovascular events and stenosis progression. RNF213 p.Arg4810Lys was found in 25% of cases, revealing distinct clinical features between carriers and non-carriers. The incidence of ipsilateral ischemic cerebrovascular events was 4.3% (6/139 cases), and stenosis progression was observed in 13% (18/139 cases) during a mean follow-up period of 58 months. Stenosis progression rates were notably higher in the RNF213 variant group (25.7%; 9/35 cases) than in the RNF213 wild-type group (8.7%; 9/104 cases). Cumulative stenosis progression rate was significantly higher in the RNF213 variant group than in the RNF213 wild-type group (log-rank test, P = 0.0004). Multivariate Cox regression analysis indicated a significant association between the RNF213 p.Arg4810Lys variant and an increased risk of stenosis progression (P = 0.03, odds ratio 3.2; 95% confidence interval, 1.1-9.0). The RNF213 p.Arg4810Lys variant exhibits clinical disparities in asymptomatic ICAS and is notably linked to a heightened risk of stenosis progression. These results suggest a distinct difference in the vascular stenosis mechanism associated with this variant, warranting further investigation into its clinical implications and potential mechanistic insights.

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来源期刊
Translational Stroke Research
Translational Stroke Research CLINICAL NEUROLOGY-NEUROSCIENCES
CiteScore
13.80
自引率
4.30%
发文量
130
审稿时长
6-12 weeks
期刊介绍: Translational Stroke Research covers basic, translational, and clinical studies. The Journal emphasizes novel approaches to help both to understand clinical phenomenon through basic science tools, and to translate basic science discoveries into the development of new strategies for the prevention, assessment, treatment, and enhancement of central nervous system repair after stroke and other forms of neurotrauma. Translational Stroke Research focuses on translational research and is relevant to both basic scientists and physicians, including but not restricted to neuroscientists, vascular biologists, neurologists, neuroimagers, and neurosurgeons.
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