Department of Laboratory Medicine, Laboratory of Cardiovascular Endocrinology and Cell Biology, Scuola Superiore Sant'Anna e Fondazione CNR - Regione Toscana G. Monasterio, Pisa, Italy.
Dipartimento di Medicina di Laboratorio, Azienda Ospedaliera Universitaria di Padova, and Dipartimento di Medicina - Università di Padova, Padova, Italy.
Clin Chem Lab Med. 2020 Nov 26;59(4):641-652. doi: 10.1515/cclm-2020-1433. Print 2021 Mar 26.
The high-sensitivity immunoassays for cardiac troponin I (hs-cTnI) and cardiac troponin T (hs-cTnT) are recommended by all the most recent international guidelines as gold standard laboratory methods for the detection of myocardial injury and diagnosis of acute myocardial infarction (AMI). In this review article, the Authors aimed at discussing the relevant biochemical, physiological, and clinical issues related to biological variability of cTnI and cTnT. Cardiac troponins, measured with hs-cTn methods, show a better clinical profile than the other cardio-specific biomarkers (such as the natriuretic peptides, BNP and NT-proBNP). In particular, the hs-cTn methods are characterized by a low intra-individual index of variation (<0.6) and reduced analytical imprecision (about 5% CV) at the clinical cut-off value (i.e., the 99th percentile URL value). Moreover, recent studies have reported that differences between two hs-cTn measured values (RCV) >30% can be considered statistically significant. These favourable biological characteristics and analytical performance of hs-cTn methods significantly improved the accuracy in the diagnostic process of acute coronary syndromes (ACS) in patients admitted to emergence department. In addition, several studies have demonstrated the clinical usefulness of cardiovascular risk evaluation with hs-cTn methods in some groups of patients with clinical conditions at high cardiovascular risk (such as systemic hypertension, severe obesity, diabetes mellitus, renal insufficiency, and chronic obstructive pulmonary disease). However, screening programs in the general population with hs-cTn methods for cardiovascular risk stratification require further investigation to define the optimal target populations, timing of measurement, and preventive interventions.
高敏心肌肌钙蛋白 I(hs-cTnI)和心肌肌钙蛋白 T(hs-cTnT)的免疫检测法被所有最新的国际指南推荐为检测心肌损伤和诊断急性心肌梗死(AMI)的金标准实验室方法。在这篇综述文章中,作者旨在讨论与 cTnI 和 cTnT 生物学变异性相关的生化、生理和临床问题。用 hs-cTn 方法测量的心肌肌钙蛋白显示出比其他心脏特异性生物标志物(如利钠肽、BNP 和 NT-proBNP)更好的临床特征。特别是,hs-cTn 方法的特点是个体内变异指数低(<0.6),在临床临界值(即 99 百分位 URL 值)时分析不精密度降低(约 5%CV)。此外,最近的研究报告称,两次 hs-cTn 测量值(RCV)之间的差异>30%可被认为具有统计学意义。hs-cTn 方法的这些有利的生物学特征和分析性能显著提高了急性冠状动脉综合征(ACS)患者在急诊就诊时的诊断准确性。此外,一些研究表明,hs-cTn 方法在一些心血管风险较高的临床情况下的患者(如高血压、严重肥胖、糖尿病、肾功能不全和慢性阻塞性肺疾病)的心血管风险评估中具有临床应用价值。然而,使用 hs-cTn 方法对普通人群进行心血管风险分层的筛查计划需要进一步研究,以确定最佳目标人群、测量时间和预防干预措施。