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专门的"Lp(a) 门诊":一个时机已到的概念?

The dedicated "Lp(a) clinic": A concept whose time has arrived?

机构信息

Vascular Medicine Program, Sulpizio Cardiovascular Center, Division of Cardiology, Department of Medicine, University of California San Diego, La Jolla, CA, USA; Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands.

Vascular Medicine Program, Sulpizio Cardiovascular Center, Division of Cardiology, Department of Medicine, University of California San Diego, La Jolla, CA, USA; Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands.

出版信息

Atherosclerosis. 2020 May;300:1-9. doi: 10.1016/j.atherosclerosis.2020.03.003. Epub 2020 Mar 13.

Abstract

The emergence of pathophysiological, epidemiologic, and genetic data strongly supports the causality for lipoprotein(a) [Lp(a)] in cardiovascular disease (CVD) and calcific aortic valve disease (CAVD). In parallel, novel Lp(a) lowering approaches have been developed that have re-invigorated clinical interest in Lp(a). Because Lp(a) is the most prevalent monogenetic lipid disorder globally, with prevalence of Lp(a) > 50 mg/dL estimated at >1.4 billion people, the rationale for diagnosing and managing Lp(a)-mediated risk is now stronger than ever. Patients with elevated Lp(a) are significantly under-diagnosed and the diagnosis is frequently made ad hoc rather than systematically. Elevated Lp(a) levels are associated with atherothrombotic risk and patients present with varied clinical phenotypes, ranging from stroke in pediatric age groups, to ST-segment elevation myocardial infarction in young males, to CAVD in elderly individuals. A new clinical care paradigm of a dedicated "Lp(a) Clinic" would serve to evaluate and manage such patients who have elevated Lp(a) as the pathophysiological etiology. Such a clinic would include multidisciplinary expertise in lipid metabolism, clinical cardiology, vascular medicine, valvular disease, thrombosis, and pediatric aspects of clinical care. This viewpoint argues for the rationale of an Lp(a) outpatient clinic where patients with elevated Lp(a) and their affected relatives can be referred, evaluated, managed and followed, to ultimately reduce Lp(a)-mediated CVD and CAVD risk.

摘要

病理生理学、流行病学和遗传学数据的出现强烈支持脂蛋白(a) [Lp(a)] 在心血管疾病 (CVD) 和钙化主动脉瓣疾病 (CAVD) 中的因果关系。与此同时,新的降低 Lp(a) 的方法已经开发出来,重新激发了人们对 Lp(a) 的临床兴趣。由于 Lp(a) 是全球最常见的单基因脂质紊乱,Lp(a) > 50mg/dL 的患病率估计超过 14 亿人,因此诊断和管理 Lp(a)介导的风险的理由比以往任何时候都更充分。患有高 Lp(a) 的患者明显被漏诊,而且诊断通常是临时做出的,而不是系统地做出的。高 Lp(a) 水平与动脉粥样硬化血栓形成风险相关,患者表现出不同的临床表型,从儿科年龄段的中风到年轻男性的 ST 段抬高型心肌梗死,再到老年患者的 CAVD。专门的“Lp(a) 诊所”的新临床护理模式将用于评估和管理患有高 Lp(a) 的患者,因为 Lp(a) 是其病理生理病因。该诊所将包括脂质代谢、临床心脏病学、血管医学、瓣膜疾病、血栓形成和儿科临床护理方面的多学科专业知识。这种观点主张建立 Lp(a) 门诊诊所的合理性,以便将患有高 Lp(a) 及其受影响亲属的患者转介、评估、管理和随访,最终降低 Lp(a) 介导的 CVD 和 CAVD 风险。

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