Alanis G A, Boutouyrie P, Abouqateb M, Bruno R M, Andrieu M, Vedie B, Geromin D, Danchin N, Laurent S, Jouven X, Empana J P
Integrative Epidemiology of Cardiovascular Disease Université Paris Cité, INSERM U970 Paris France.
Paris Cardiovascular Research Centre, Team Arterial Diseases in Women Université Paris Cité, INSERM U970 Paris France.
J Am Heart Assoc. 2025 Apr;14(7):e037718. doi: 10.1161/JAHA.124.037718. Epub 2025 Mar 27.
We examined the association between clusters of vascular aging manifestations and ultrasensitivity cardiac troponin I in individuals without cardiovascular disease.
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.
Vascular aging manifestations of arteriosclerosis and atherosclerosis may partly explain the release of troponin I into the bloodstream in adults without clinical cardiovascular disease.
URL: https://clinicaltrials.gov; Unique identifier: NCT00741728.
我们研究了无心血管疾病个体的血管老化表现簇与超敏心肌肌钙蛋白I之间的关联。
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,该法国队列有10157名参与者。采用检测限为0.013 pg/mL的超敏免疫测定法测量心肌肌钙蛋白I。通过对右颈总动脉进行回声跟踪来评估血管老化表现,以测量结构和功能参数。采用层次聚类法识别血管老化簇。多项回归分析评估血管老化簇与心肌肌钙蛋白I五分位数之间的关联。该研究纳入了8722名无心血管疾病的参与者(平均年龄±标准差为59.5±6.3岁;女性占39%)。识别出三个血管老化簇。簇1(n = 4158;47.4%)的特征为健康的血管老化,动脉硬化和动脉粥样硬化指数最低;簇2(n = 2237;25.5%)的特征是动脉硬化指数最高,包括脉搏波速度、β指数和杨氏弹性模量增加,扩张系数最低;簇3(n = 2377;27.0%)的特征是动脉粥样硬化指数最高,包括斑块患病率更高和内膜中层厚度更大。与健康的血管老化相比,动脉硬化和动脉粥样硬化簇与心肌肌钙蛋白I五分位数呈分级正相关,且独立于传统危险因素。对于动脉硬化簇,属于最高五分位数(五分位数5与五分位数1相比)的调整优势比为1.55(95%CI,1.31 - 1.92),对于动脉粥样硬化簇为2.66(95%CI,2.18 - 3.23)。
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在无临床心血管疾病的成年人中肌钙蛋白I释放到血液中的现象。