Department of Cardiology, Hospital Clínico Universitario Virgen de la Arrixaca, Instituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), CIBERCV, University of Murcia, Murcia, Spain.
Department of Hematology and Clinical Oncology, Hospital Universitario Morales Meseguer, Instituto Murciano de Investigación Biosanitaria (IMIB-Arrixaca), University of Murcia, Murcia, Spain.
Thromb Haemost. 2019 Dec;119(12):1901-1919. doi: 10.1055/s-0039-1696955. Epub 2019 Sep 9.
In cardiovascular disease (CVD), biomarkers (i.e., "biological markers") could have multiple roles in understanding the complexity of cardiovascular (CV) pathophysiology and to offer an integrated approach to management. Biomarkers could help in daily practice as a diagnostic tool, to monitor therapy response, to assess prognosis and as early marker of CV damage, or to stratify risk. In recent years, the role of biomarkers in CVD is even more relevant and some have recently been included in clinical management guideline recommendations. The aim of this review is to discuss the recommendations in clinical guidelines of various biomarkers and to review their usefulness in daily clinical practice. Ultimately, a balance is needed between simplicity and practicality for clinical decision-making. Most biomarkers (whether blood, urine, or imaging-based) will improve on clinical risk stratification, but awaiting biomarker results may lead to delays in the initiation of therapy, for example, anticoagulation for stroke prevention in atrial fibrillation. Many biomarkers are nonspecific, being predictive of many CV and non-CV outcomes, so would be better as "rule-out" rather than "rule-in" assessments. Derivation of some biomarkers have also been made in highly selected clinical trial cohorts, where measurement is made at baseline but outcomes determined many years later; given the dynamic nature of risk in the "real world" where patients get older and develop incident risk factors, this may give a false impression of the risk profile. Finally, some laboratory biomarkers have a diurnal variation and inter-/intravariability (and lower limits of detection) in assays, which may be expensive, are added considerations.
在心血管疾病 (CVD) 中,生物标志物(即“生物标记物”)在理解心血管 (CV) 病理生理学的复杂性方面可以发挥多种作用,并提供综合的管理方法。生物标志物可以作为诊断工具在日常实践中提供帮助,用于监测治疗反应,评估预后和作为 CV 损伤的早期标志物,或进行风险分层。近年来,生物标志物在 CVD 中的作用更加重要,其中一些最近已被纳入临床管理指南建议。本综述的目的是讨论各种生物标志物临床指南中的建议,并回顾它们在日常临床实践中的用途。最终,需要在临床决策的简单性和实用性之间取得平衡。大多数生物标志物(无论是血液、尿液还是基于成像的)都将改善临床风险分层,但等待生物标志物结果可能会导致治疗开始延迟,例如在心房颤动中预防中风的抗凝治疗。许多生物标志物是非特异性的,可预测许多 CV 和非 CV 结局,因此最好作为“排除”而不是“纳入”评估。一些生物标志物的推导也是在高度选择的临床试验队列中进行的,其中在基线时进行测量,但在多年后确定结局;鉴于在“现实世界”中患者年龄增长并出现新的风险因素的情况下风险的动态性质,这可能会对风险状况产生错误印象。最后,一些实验室生物标志物在检测中存在昼夜变化和个体/个体内变异性(以及检测下限),这可能很昂贵,这是需要考虑的额外因素。