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利用循环生物标志物改善心房颤动患者的卒中风险预测:CHADS-VASc-生物标志物模型

Improving stroke risk prediction in atrial fibrillation with circulating biomarkers: the CHADS-VASc-Biomarkers model.

作者信息

Short Samuel A P, Wilkinson Katherine, Hald Erin, Howard George, Howard Virginia, Judd Suzanne E, Soliman Elsayed Z, Kissela Brett, Robinson David, Stanton Robert, Cushman Mary

机构信息

Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.

Department of Pathology and Laboratory Medicine, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.

出版信息

J Thromb Haemost. 2025 Aug 1. doi: 10.1016/j.jtha.2025.06.007.

Abstract

BACKGROUND

Anticoagulation reduces ischemic stroke in atrial fibrillation (AF) but increases bleeding. Existing risk calculators guiding anticoagulation decisions in AF have substantial limitations.

OBJECTIVES

To determine whether biomarkers of stroke risk for general populations are associated with stroke risk in AF and improve predictive performance of the CHADS-VASc (Congestive heart failure, Hypertension, Age >74, Diabetes, prior Stroke or transient ischemic attack or thromboembolism, Vascular disease, Age 65-74, Sex category) score.

METHODS

The REasons for Geographic And Racial Differences in Stroke (REGARDS) is a prospective cohort study of 30 239 adults enrolled in 2003 to 2007 and monitored for stroke. Participants with AF not taking anticoagulants and with no prior stroke history were studied. Nine circulating biomarkers were measured in stored baseline samples. Cox models, adjusted for demographics and stroke risk factors estimated associations of each biomarker with incident stroke. Then, models with CHADS-VASc score alone or adding biomarkers were compared using tests of fit (likelihood ratio test and Akaike information criterion) and risk discrimination (continuous net reclassification index, [NRI]).

RESULTS

Among 2411 participants with AF (median age 69 years, 55% female, 36% Black), 163 (7%) developed first-time ischemic stroke over 13 years. Higher N-terminal pro-B-type natriuretic peptide, growth differentiation factor 15, cystatin C, interleukin 6, and lipoprotein (a) were independently associated with higher stroke risk. Biomarkers substantially improved CHADS-VASc model fit (change in Akaike information criterion -13, P < .001) and predictive ability (5-year NRI 0.42). Adding only N-terminal pro-B-type natriuretic peptide and growth differentiation factor 15 yielded the best model fit and a similar NRI compared with all biomarkers.

CONCLUSIONS

Five biomarkers were associated with stroke risk in AF, and 2 of these improved CHADS-VASc performance. This improved CHADS-VASc-Biomarkers score can allow better selection of patients for anticoagulation to reduce stroke in AF.

摘要

背景

抗凝治疗可降低心房颤动(AF)患者的缺血性卒中风险,但会增加出血风险。现有的指导AF抗凝决策的风险计算器存在很大局限性。

目的

确定一般人群的卒中风险生物标志物是否与AF患者的卒中风险相关,并改善CHADS-VASc(充血性心力衰竭、高血压、年龄>74岁、糖尿病、既往卒中或短暂性脑缺血发作或血栓栓塞、血管疾病、年龄65-74岁、性别类别)评分的预测性能。

方法

“卒中地理和种族差异原因(REGARDS)”研究是一项对2003年至2007年纳入的30239名成年人进行的前瞻性队列研究,对其进行卒中监测。研究对象为未服用抗凝剂且无既往卒中史的AF患者。在储存的基线样本中测量了9种循环生物标志物。Cox模型在对人口统计学和卒中风险因素进行调整后,估计每种生物标志物与卒中事件的关联。然后,使用拟合检验(似然比检验和赤池信息准则)和风险辨别(连续净重新分类指数,[NRI])比较仅使用CHADS-VASc评分或添加生物标志物的模型。

结果

在2411名AF患者(中位年龄69岁,55%为女性,36%为黑人)中,163名(7%)在13年中发生了首次缺血性卒中。较高的N末端B型利钠肽原、生长分化因子15、胱抑素C、白细胞介素6和脂蛋白(a)与较高的卒中风险独立相关。生物标志物显著改善了CHADS-VASc模型的拟合度(赤池信息准则变化-13,P<.001)和预测能力(5年NRI为0.42)。仅添加N末端B型利钠肽原和生长分化因子15产生了最佳的模型拟合度,与所有生物标志物相比,NRI相似。

结论

五种生物标志物与AF患者的卒中风险相关,其中两种改善了CHADS-VASc的性能。这种改进的CHADS-VASc-生物标志物评分可以更好地选择接受抗凝治疗的患者,以降低AF患者的卒中风险。

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