Cardiac markers: present and future.

M Plebani, M Zaninotto
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引用次数: 29

Abstract

In the early twentieth century, acute myocardial infarction secondary to acute thrombotic coronary occlusion was considered a rare, fatal condition. Acute myocardial infarction is now one of the most-commmon serious illnesses in the industrialized world. Laboratory medicine now plays a crucial role in identifying risk factors, early events, and conditions triggering plaque rupture in coronary ischemic disease. However, the greatest progress in laboratory research has resulted from the discovery of new and more-promising biochemical markers of myocardial damage. The discovery of cardiac troponins, in particular, has heralded a new age in the diagnosis and treatment or management of a broad spectrum of diseases, grouped together under the heading of acute coronary syndrome, and including stable and unstable angina, and non-Q wave infarction to Q-wave infarction. Cardiac troponins, which are selectively released by damaged myocardiocytes, have a specificity that has not only allowed an improvement in the diagnosis of acute cardiac ischemic disorders, but has also enabled us to make a more-reliable stratification of risk and prediction of outcome. It is generally agreed that two biochemical markers should be used: an early marker (and we recommed myoglobin for this) and a definitive marker, which is cardiac troponin (I or T). Future research is likely to include the standardization of methods for measuring current markers, troponin I in particular, the assessment of rapid bedside tests, and the investigation of the relationship between cardiac markers and emerging immunological and coagulation parameters. Thrombogenesis is now recognized as important in the final process of coronary atherosclerosis, and new markers of thrombogenesis should be used to evaluate the risk of plaque rupture and to monitor the outcome of thrombolytic therapy. Moreover, recent vascular biology studies have provided information on the developmental stages of atherosclerosis and emphasized the importance of the endothelium as a modulator of vascular reactivity, atherogenesis, and plaque stability. The different types of laboratory test (biochemical, immunological, and coagulative) now available, should soon allow improvement in the diagnosis and therapy of ischemic coronary diseases.

心脏标志物:现在和未来。
在二十世纪早期,急性血栓性冠状动脉闭塞继发急性心肌梗死被认为是一种罕见的、致命的疾病。急性心肌梗塞现在是工业化国家最常见的严重疾病之一。检验医学现在在确定引发冠状动脉缺血性疾病斑块破裂的危险因素、早期事件和条件方面起着至关重要的作用。然而,实验室研究的最大进展是由于发现了新的和更有前途的心肌损伤生化标志物。特别是心肌肌钙蛋白的发现,预示着广泛疾病的诊断和治疗或管理的新时代,这些疾病在急性冠脉综合征的标题下分组在一起,包括稳定型和不稳定型心绞痛,以及非q波梗死到q波梗死。心肌肌钙蛋白是由受损心肌细胞选择性释放的,它具有特异性,不仅可以改善急性心肌缺血性疾病的诊断,而且还使我们能够进行更可靠的风险分层和结果预测。人们普遍认为应该使用两种生化标志物:一种是早期标志物(我们推荐使用肌红蛋白),另一种是最终标志物,即心肌肌钙蛋白(I或T)。未来的研究可能包括对当前标志物(尤其是肌钙蛋白I)测量方法的标准化,对快速床边试验的评估,以及心脏标志物与新出现的免疫和凝血参数之间关系的研究。血栓形成现在被认为在冠状动脉粥样硬化的最终过程中是重要的,血栓形成的新标志物应该用于评估斑块破裂的风险和监测溶栓治疗的结果。此外,最近的血管生物学研究提供了动脉粥样硬化发育阶段的信息,并强调了内皮作为血管反应性、动脉粥样硬化发生和斑块稳定性调节剂的重要性。不同类型的实验室测试(生化、免疫和凝固)现在可用,应该很快允许改进缺血性冠状动脉疾病的诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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