Department of Cardiology, Kanazawa University Graduate School of Medical Science.
J Atheroscler Thromb. 2019 Jul 1;26(7):583-591. doi: 10.5551/jat.RV17034. Epub 2019 Apr 30.
Lipoprotein(a) [Lp(a)], discovered in 1963, has been associated with atherosclerotic cardiovascular disease (ASCVD) independent of other traditional risk factors, including LDL cholesterol. Lp(a) is an apolipoprotein B (apoB)-containing lipoprotein, which contains an LDL-like particle. Unlike LDL, which is a primary therapeutic target to decrease ASCVD, current guidelines recommend measuring Lp(a) for risk assessments because there is no clear evidence demonstrating the clinical benefit of decreasing Lp(a) using classical drugs such as niacin. However, recent Mendelian randomization studies indicate that Lp(a) causally correlates with ASCVD. In addition, novel drugs, including PCSK9 inhibitors, as well as antisense oligonucleotide for apo(a), have exhibited efficacy in decreasing Lp(a) substantially, invigorating a discussion whether Lp(a) could be a novel therapeutic target for further ASCVD risk reduction. This review aims to provide current understanding, and future perspectives, of Lp(a), which is currently considered a mere biomarker but may emerge as a novel therapeutic target in future clinical settings.
脂蛋白(a)[Lp(a)]于 1963 年被发现,与动脉粥样硬化性心血管疾病(ASCVD)相关,独立于其他传统危险因素,包括 LDL 胆固醇。Lp(a)是载脂蛋白 B(apoB)的脂蛋白,含有 LDL 样颗粒。与 LDL 不同,LDL 是降低 ASCVD 的主要治疗靶点,目前的指南建议测量 Lp(a)进行风险评估,因为没有明确的证据表明使用烟酸等经典药物降低 Lp(a)具有临床益处。然而,最近的孟德尔随机研究表明,Lp(a)与 ASCVD 有因果关系。此外,新型药物,包括 PCSK9 抑制剂和针对 apo(a)的反义寡核苷酸,已显示出显著降低 Lp(a)的疗效,这引发了关于 Lp(a)是否可以成为进一步降低 ASCVD 风险的新治疗靶点的讨论。本文旨在提供目前对 Lp(a)的理解和未来展望,Lp(a)目前被认为只是一种生物标志物,但在未来的临床环境中可能会成为一种新的治疗靶点。