Morello Fulvio, Piler Pavel, Novak Miroslav, Kruzliak Peter
Emergency Department, A.O. Città della Salute e della Scienza, Molinette Hospital, Turin, Italy.
Biomark Med. 2014;8(7):931-41. doi: 10.2217/bmm.14.38.
Aortic dissection (AD) is a severe vascular disease associated with major morbidity and mortality. The diagnosis of AD requires the performance of urgent aortic imaging exams such as computed tomography angiography, but the decision to perform these exams now essentially relies on clinical judgment. Several studies have identified a range of potential biomarkers stemming from the aortic extracellular matrix (matrix metalloproteinases, TGF-β, soluble elastin fragments), vascular smooth muscle cells (smooth muscle myosin heavy chain, creatine kinase, calponin), coagulation (D-dimer, platelets) and inflammation (C-reactive protein), whose circulating levels increase in patients affected by AD. Biomarkers of AD could be potentially used to screen patients with compatible symptoms, to identify patients at higher risk of AD, to rule out AD in patients with non-high clinical probability of AD and/or to obtain prognostic stratification of affected patients. This review will summarize available data and discuss present and future perspectives of circulating biomarkers for the diagnosis and prognostic stratification of AD.
主动脉夹层(AD)是一种严重的血管疾病,与高发病率和死亡率相关。AD的诊断需要进行紧急主动脉成像检查,如计算机断层血管造影,但现在决定进行这些检查基本上依赖于临床判断。几项研究已经确定了一系列源自主动脉细胞外基质(基质金属蛋白酶、转化生长因子-β、可溶性弹性蛋白片段)、血管平滑肌细胞(平滑肌肌球蛋白重链、肌酸激酶、钙调蛋白)、凝血(D-二聚体、血小板)和炎症(C反应蛋白)的潜在生物标志物,其在AD患者中的循环水平会升高。AD的生物标志物可能潜在地用于筛查有相容症状的患者、识别AD风险较高的患者、排除AD临床可能性不高的患者和/或对受影响患者进行预后分层。本综述将总结现有数据,并讨论循环生物标志物在AD诊断和预后分层方面的现状和未来前景。