Mansoor Taha, Rao Bassam Hamid, Gupta Kartik, Parikh Sachin S, Abramov Dmitry, Mehta Anurag, Al Rifai Mahmoud, Virani Salim S, Nambi Vijay, Minhas Abdul Mannan Khan, Koshy Santhosh K G
Department of Internal Medicine, Western Michigan University Homer Stryker M.D. School of Medicine, 1000 Oakland Dr, Kalamazoo, MI, USA.
Shifa College of Medicine, Islamabad, Pakistan.
Am J Cardiovasc Drugs. 2025 May;25(3):293-306. doi: 10.1007/s40256-024-00712-x. Epub 2024 Dec 20.
Reducing low-density lipoprotein cholesterol (LDL-C) levels has been shown to reduce the risk of developing atherosclerotic cardiovascular disease (ASCVD). Statins are the foundation of LDL-C lowering therapy with other non-statin agents used in circumstances where goal LDL-C levels are not reached or owing to intolerance to adverse effects of statins. In 2003, the discovery of the role of the proprotein convertase subtilisin/kexin type 9 (PCSK9) system in promoting elevated LDL-C levels led to new avenues of drug development to achieve target LDL-C. In 2021, inclisiran, a small interfering ribonucleic acid (siRNA) molecule targeting PCSK9 was approved by the Food and Drug Administration (FDA). Inclisiran has demonstrated effective reductions of LDL-C, such as in the large phase-3 ORION-9, ORION-10, and ORION-11 trials in which it achieved LDL-C reductions of 39.7%, 52.3%, and 49.9%, respectively. This review discusses the current clinical evidence and ongoing clinical studies of inclisiran as well as analyzes other areas of PCSK9 inhibition development.
降低低密度脂蛋白胆固醇(LDL-C)水平已被证明可降低发生动脉粥样硬化性心血管疾病(ASCVD)的风险。他汀类药物是降低LDL-C治疗的基础,在未达到目标LDL-C水平或因对他汀类药物不良反应不耐受的情况下,可使用其他非他汀类药物。2003年,前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)系统在促进LDL-C水平升高方面作用的发现,为实现目标LDL-C开辟了新的药物研发途径。2021年,一种靶向PCSK9的小干扰核糖核酸(siRNA)分子inclisiran获得美国食品药品监督管理局(FDA)批准。inclisiran已证明能有效降低LDL-C水平,如在大型3期ORION-9、ORION-10和ORION-11试验中,它分别使LDL-C降低了39.7%、52.3%和49.9%。本综述讨论了inclisiran目前的临床证据和正在进行的临床研究,并分析了PCSK9抑制开发的其他领域。