作为药理靶点的脂蛋白(a):前提、承诺和前景。

IF 38.6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation Pub Date : 2025-02-11 Epub Date: 2025-02-10 DOI:10.1161/CIRCULATIONAHA.124.069210
Antonio Greco, Simone Finocchiaro, Marco Spagnolo, Denise Cristiana Faro, Maria Sara Mauro, Carmelo Raffo, Giuseppe Sangiorgio, Antonino Imbesi, Claudio Laudani, Placido Maria Mazzone, Nicola Ammirabile, Daniele Giacoppo, Davide Landolina, Davide Capodanno
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引用次数: 0

摘要

动脉粥样硬化性心血管疾病是世界范围内的主要健康问题,需要有效的预防措施。脂蛋白(脂蛋白[a])作为动脉粥样硬化性心血管疾病的独立危险因素最近引起了人们的关注,其促炎和促血栓机制有助于其动脉粥样硬化性。在等摩尔的基础上,Lp(a)的致动脉粥样硬化性是与心血管不良后果广泛相关的颗粒(如LDL(低密度脂蛋白))的5至6倍。Lp(a)可以进入血管壁,导致氧化磷脂在动脉内膜积聚,这对于启动斑块炎症和触发血管疾病进展至关重要。此外,Lp(a)可能通过载脂蛋白a (apoA)与血小板PAR-1(蛋白酶激活受体1)受体的相互作用以及对纤溶酶原的竞争性抑制而引起动脉粥样硬化血栓形成。由于Lp(a)主要是由遗传基础决定的,因此一生中进行一次评估就足以确定患者是否有升高的水平。孟德尔随机化研究和LDL降胆固醇药物随机试验的事后分析表明,Lp(a)浓度与心血管结局之间存在因果关系,治疗性降低Lp(a)有望有助于估计的心血管风险缓解。许多降低Lp(a)的药物,包括单克隆抗体、小干扰核糖核酸、反义寡核苷酸、小分子和基因编辑化合物,都处于临床研究的不同阶段,并显示出临床应用的希望。特别是,Lp(a)检测和治疗的增加预计将在人群水平上产生重大影响,从而能够识别高风险个体并随后预防大量心血管事件。正在进行的3期试验将进一步阐明长期降低Lp(a)对心血管的益处,为有针对性的干预和改善心血管结局提供潜在途径。
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Lipoprotein(a) as a Pharmacological Target: Premises, Promises, and Prospects.

Atherosclerotic cardiovascular disease is a major health concern worldwide and requires effective preventive measures. Lp(a) (lipoprotein [a]) has recently garnered attention as an independent risk factor for astherosclerotic cardiovascular disease, with proinflammatory and prothrombotic mechanisms contributing to its atherogenicity. On an equimolar basis, Lp(a) is ~5 to 6 times more atherogenic than particles that have been widely associated with adverse cardiovascular outcomes, such as LDL (low-density lipoprotein). Lp(a) can enter the vessel wall, leading to the accumulation of oxidized phospholipids in the arterial intima, which are crucial for initiating plaque inflammation and triggering vascular disease progression. In addition, Lp(a) may cause atherothrombosis through interactions between apoA (apolipoprotein A) and the platelet PAR-1 (protease-activated receptor 1) receptor, as well as competitive inhibition of plasminogen. Because Lp(a) is mostly determined on genetic bases, a 1-time assessment in a lifetime can suffice to identify patients with elevated levels. Mendelian randomization studies and post hoc analyses of randomized trials of LDL cholesterol-lowering drugs showed a causal link between Lp(a) concentrations and cardiovascular outcomes, with therapeutic reduction of Lp(a) expected to contribute to estimated cardiovascular risk mitigation. Many Lp(a)-lowering drugs, including monoclonal antibodies, small interfering ribonucleic acids, antisense oligonucleotides, small molecules, and gene editing compounds, are at different stages of clinical investigation and show promise for clinical use. In particular, increased Lp(a) testing and treatment are expected to have a substantial impact at the population level, enabling the identification of high-risk individuals and the subsequent prevention of a large number of cardiovascular events. Ongoing phase 3 trials will further elucidate the cardiovascular benefits of Lp(a) reduction over the long term, offering potential avenues for targeted interventions and improved cardiovascular outcomes.

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来源期刊
Circulation
Circulation 医学-外周血管病
CiteScore
45.70
自引率
2.10%
发文量
1473
审稿时长
2 months
期刊介绍: Circulation is a platform that publishes a diverse range of content related to cardiovascular health and disease. This includes original research manuscripts, review articles, and other contributions spanning observational studies, clinical trials, epidemiology, health services, outcomes studies, and advancements in basic and translational research. The journal serves as a vital resource for professionals and researchers in the field of cardiovascular health, providing a comprehensive platform for disseminating knowledge and fostering advancements in the understanding and management of cardiovascular issues.
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