在没有临床表现的心肌损伤情况下,血管加速老化是肌钙蛋白I释放的可能机制。

IF 5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Journal of the American Heart Association Pub Date : 2025-04-01 Epub Date: 2025-03-27 DOI:10.1161/JAHA.124.037718
G A Alanis, P Boutouyrie, M Abouqateb, R M Bruno, M Andrieu, B Vedie, D Geromin, N Danchin, S Laurent, X Jouven, J P Empana
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引用次数: 0

摘要

背景:在无心血管疾病的个体中,我们研究了血管老化表现簇与心肌肌钙蛋白I超敏感性之间的关系。方法和结果:使用来自PPS-3(巴黎前瞻性研究III)的基线数据进行横断面分析,该研究是一项法国队列研究,共有10157名参与者。采用超灵敏免疫分析法测定心肌肌钙蛋白I,检测限为0.013 pg/mL。血管老化的表现通过回声追踪右颈总动脉测量结构和功能参数进行评估。采用分层聚类方法对血管老化进行分类。多项回归评估血管老化簇与心肌肌钙蛋白I五分位数之间的关系。该研究纳入了8722名无心血管疾病的参与者(平均±SD年龄,59.5±6.3岁;39%的女性)。确定了三种血管老化簇。集群1 (n=4158;47.4%)为健康血管老化,动脉硬化和动脉粥样硬化指数最低;聚类2 (n=2237;25.5%)动脉硬化指标最高,脉搏波速、β指数、杨氏弹性模量升高,扩张系数最低;聚类3 (n=2377;27.0%)的特点是动脉粥样硬化指数最高,包括更频繁的斑块患病率和更大的内膜-中膜厚度。与健康血管老化相比,动脉硬化和动脉粥样硬化簇与心肌肌钙蛋白I呈分级正相关,独立于传统危险因素。动脉硬化患者属于最高五分位数(五分位数5 vs五分位数1)的调整优势比为1.55 (95% CI, 1.31-1.92),动脉粥样硬化组为2.66 (95% CI, 2.18-3.23)。结论:动脉硬化和动脉粥样硬化的血管老化表现可能部分解释了肌钙蛋白I在没有临床心血管疾病的成年人中释放到血液中的原因。注册:网址:https://clinicaltrials.gov;唯一标识符:NCT00741728。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Accelerated Vascular Aging as a Possible Mechanism of Troponin I Release in the Absence of Clinically Manifested Myocardial Injury.

Background: We examined the association between clusters of vascular aging manifestations and ultrasensitivity cardiac troponin I in individuals without cardiovascular disease.

Methods and results: A cross-sectional analysis was conducted using baseline data from PPS-3 (Paris Prospective Study III), a French cohort of 10 157 participants. Cardiac troponin I was measured with an ultrasensitive immunoassay with a limit of detection of 0.013 pg/mL. Vascular aging manifestations were assessed via echotracking of the right common carotid artery to measure structural and functional parameters. Hierarchical clustering was used to identify clusters of vascular aging. Multinomial regression assessed the association between vascular aging clusters and cardiac troponin I quintiles. The study included 8722 cardiovascular disease-free participants (mean±SD age, 59.5±6.3 years; 39% women). Three vascular aging clusters were identified. Cluster 1 (n=4158; 47.4%) was characterized as healthy vascular aging with the lowest arteriosclerosis and atherosclerosis indices; cluster 2 (n=2237; 25.5%) was characterized by the highest arteriosclerosis indices, including increased pulse wave velocity, β index, and Young elastic modulus and lowest distensibility coefficient; and cluster 3 (n=2377; 27.0%) was characterized by the highest atherosclerosis indices, including more frequent plaque prevalence and greater intima-media thickness. Compared with healthy vascular aging, arteriosclerosis and atherosclerosis clusters showed a graded positive association with cardiac troponin I quintiles, independent of traditional risk factors. The adjusted odds ratio for belonging to the highest quintile (quintile 5 versus quintile 1) was 1.55 (95% CI, 1.31-1.92) for arteriosclerosis and 2.66 (95% CI, 2.18-3.23) for atherosclerosis clusters.

Conclusions: Vascular aging manifestations of arteriosclerosis and atherosclerosis may partly explain the release of troponin I into the bloodstream in adults without clinical cardiovascular disease.

Registration: URL: https://clinicaltrials.gov; Unique identifier: NCT00741728.

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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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