Parikh Shailja V, de Lemos James A
Department of Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9047, USA.
Am J Med Sci. 2006 Oct;332(4):186-97. doi: 10.1097/00000441-200610000-00006.
Biomarkers play an important role in the diagnosis, prognostic assessment, and management of patients with suspected acute coronary syndromes (ACS). Specific biomarkers identify different components of the pathophysiology of ACS: troponins are prototype markers of myocyte necrosis, natriuretic peptides reflect neurohormonal activation and hemodynamic stress, soluble CD40 ligand is an indicator of platelet activation, and C-reactive protein, myeloperoxidase, and monocyte chemoattractant protein-1 reflect various inflammatory processes. When combined, multiple biomarkers reflecting different pathophysiologic processes appear to enhance risk stratification, as compared with using individual markers alone. Advances in proteomic technology promise to identify additional novel biomarkers that facilitate diagnosis, risk stratification, and selection of therapies in ACS. In the future, it is hoped that multiple biomarker panels will form the basis of an individualized approach to the treatment of ACS, in which therapy is tailored to individual biomarker profiles.
生物标志物在疑似急性冠脉综合征(ACS)患者的诊断、预后评估及管理中发挥着重要作用。特定的生物标志物可识别ACS病理生理学的不同组成部分:肌钙蛋白是心肌细胞坏死的典型标志物,利钠肽反映神经激素激活和血流动力学应激,可溶性CD40配体是血小板激活的指标,而C反应蛋白、髓过氧化物酶和单核细胞趋化蛋白-1反映各种炎症过程。与单独使用单个标志物相比,联合使用反映不同病理生理过程的多种生物标志物似乎可增强风险分层。蛋白质组学技术的进展有望识别出更多有助于ACS诊断、风险分层及治疗选择的新型生物标志物。未来,希望多种生物标志物组合能成为ACS个体化治疗方法的基础,即根据个体生物标志物谱量身定制治疗方案。