探索c反应蛋白变化与卒中风险之间的联系:来自前瞻性队列研究和遗传证据的见解。

IF 5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Journal of the American Heart Association Pub Date : 2025-04-01 Epub Date: 2025-03-26 DOI:10.1161/JAHA.124.038086
Yitong Ling, Shiqi Yuan, Hongtao Cheng, Shanyuan Tan, Xiaxuan Huang, Yonglan Tang, Zihong Bai, Rui Li, Li Li, Shuna Li, Liying Huang, Anding Xu, Jun Lyu
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引用次数: 0

摘要

背景:之前关于CRP (c反应蛋白)水平变化如何预测卒中风险的研究是有限的。本研究旨在探讨CRP变化与卒中及其亚型风险之间的关系。方法与结果:基于英国生物银行(UK Biobank)数据,采用Cox比例风险回归分析,探讨CRP变化与卒中及其亚型风险的关系。我们进一步进行遗传分析,包括遗传相关性、两两全基因组关联研究和多基因风险评分。我们的研究涉及14754名参与者,中位随访时间为10.4年。根据CRP百分比变化对参与者进行分类并对潜在混杂因素进行调整后,观察到CRP变化百分比升高的患者发生任何中风(危险比[HR], 1.44 [95% CI, 1.12-1.85])和缺血性中风(HR, 1.65 [95% CI, 1.24-2.18])的风险更高。根据CRP变化类型分类并调整混杂因素后,高水平组卒中风险较高(HR, 1.45 [95% CI, 1.04-2.02]),高水平组卒中风险最高(HR, 1.74 [95% CI, 1.30-2.33])。缺血性中风也有类似的趋势。保持高水平的组出血性卒中风险也增加(HR, 1.91 [95% CI, 1.07-3.44])。遗传分析显示,CRP与脑卒中有显著的遗传相关性(rg, 0.257;rg_P = 2.39 e-07)。两两全基因组关联研究分析确定了CRP与中风之间的5个共享基因组区域。多基因风险评分分析显示,卒中多基因风险评分高、CRP水平升高或保持高水平的参与者卒中风险最高。结论:任何脑卒中和缺血性脑卒中均与CRP水平升高和保持高水平有关,而出血性脑卒中仅与CRP水平保持高水平有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the Link Between C-Reactive Protein Change and Stroke Risk: Insights From a Prospective Cohort Study and Genetic Evidence.

Background: Previous research on how changes in CRP (C-reactive protein) levels predict stroke risk is limited. This study aimed to examine the association between CRP change and the risk of stroke and its subtypes.

Methods and results: Based on the UK Biobank data, we investigated the association between CRP change and the risk of stroke and its subtypes with Cox proportional hazards regression analysis. We further performed genetic analyses including genetic correlation, pairwise genome-wide association study, and polygenic risk score. Our study involved 14 754 participants with a median follow-up time of 10.4 years. After categorizing participants by CRP percentage change and making adjustments for potential confounders, it was observed that those with an elevated percentage of CRP change had a higher risk of any stroke (hazard ratio [HR], 1.44 [95% CI, 1.12-1.85]) and ischemic stroke (HR, 1.65 [95% CI, 1.24-2.18]). After categorization by CRP change types and adjustment for confounders, the group that became high level had a higher any-stroke risk (HR, 1.45 [95% CI, 1.04-2.02]), with the group that remained at a high level facing the greatest risk (HR, 1.74 [95% CI, 1.30-2.33]). Similar trends were observed for ischemic stroke. The group that remained at a high level also had a heightened hemorrhagic stroke risk (HR, 1.91 [95% CI, 1.07-3.44]). Genetic analysis showed a significant genetic correlation between CRP and stroke (rg, 0.257; rg_P=2.39E-07). Pairwise genome-wide association study analysis identified 5 shared genomic regions between CRP and stroke. Polygenic risk score analysis showed that participants with high stroke polygenic risk score and elevated or remaining high CRP levels have the highest risk of stroke.

Conclusions: Both any stroke and ischemic stroke are related to elevated and remaining high CRP levels, while hemorrhagic stroke is only related to remaining high CRP levels.

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来源期刊
Journal of the American Heart Association
Journal of the American Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
9.40
自引率
1.90%
发文量
1749
审稿时长
12 weeks
期刊介绍: As an Open Access journal, JAHA - Journal of the American Heart Association is rapidly and freely available, accelerating the translation of strong science into effective practice. JAHA is an authoritative, peer-reviewed Open Access journal focusing on cardiovascular and cerebrovascular disease. JAHA provides a global forum for basic and clinical research and timely reviews on cardiovascular disease and stroke. As an Open Access journal, its content is free on publication to read, download, and share, accelerating the translation of strong science into effective practice.
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