Giordano Salvatore, Ielapi Jessica, Salerno Nadia, Cersosimo Angelica, Lucchino Alessandro, Laschera Alessandro, Canino Giovanni, Di Costanzo Assunta, De Rosa Salvatore, Torella Daniele, Sorrentino Sabato
Department of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Department of Experimental and Clinical Medicine, "Magna Graecia" University, 88100 Catanzaro, Italy.
Rev Cardiovasc Med. 2024 Oct 22;25(10):374. doi: 10.31083/j.rcm2510374. eCollection 2024 Oct.
Acute coronary syndromes (ACSs) represent a significant global health challenge arising from atherosclerotic cardiovascular disease (ASCVD), with elevated low-density lipoprotein cholesterol (LDL-C) levels being a primary contributor. Despite standard statin therapy, individuals with ACS remain at high risk for recurrent cardiovascular events, particularly in the initial post-ACS period. Monoclonal antibodies targeting proprotein convertase subtilisin/kexin type 9 (PCSK9), such as evolocumab and alirocumab, offer a potential strategy to reduce LDL-C levels further and mitigate this residual risk. This review delves into the molecular mechanisms, effects on cholesterol metabolism, inflammatory modulation, and clinical outcomes associated with early administration of PCSK9 inhibitors following ACS.
急性冠状动脉综合征(ACS)是动脉粥样硬化性心血管疾病(ASCVD)引发的一项重大全球健康挑战,低密度脂蛋白胆固醇(LDL-C)水平升高是主要促成因素。尽管采用了标准他汀类药物治疗,但ACS患者仍面临心血管事件复发的高风险,尤其是在ACS后的初始阶段。靶向前蛋白转化酶枯草溶菌素/九型(PCSK9)的单克隆抗体,如依洛尤单抗和阿利西尤单抗,为进一步降低LDL-C水平和减轻这种残余风险提供了一种潜在策略。本综述深入探讨了ACS后早期使用PCSK9抑制剂的分子机制、对胆固醇代谢的影响、炎症调节以及临床结局。