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英克西兰:高胆固醇血症综述

Inclisiran: A Review in Hypercholesterolemia.

作者信息

Frampton James E

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Am J Cardiovasc Drugs. 2023 Mar;23(2):219-230. doi: 10.1007/s40256-023-00568-7. Epub 2023 Mar 4.

Abstract

Inclisiran (Leqvio) is a first-in-class, subcutaneously administered, small interfering RNA (siRNA) that prevents hepatic synthesis of proprotein convertase subtilisin/kexin type 9 (PCSK9), thereby decreasing circulating low-density lipoprotein cholesterol (LDL-C). In the EU, inclisiran is indicated in adults with primary hypercholesterolemia or mixed dyslipidemia, as an adjunct to diet. It is intended for use in patients unable to reach LDL-C goals on maximally tolerated statin therapy, with or without other lipid-lowering therapies (LLTs). In patients who are statin intolerant or for whom a statin is contraindicated, it can be used with or without other LLTs. In clinical trials, twice-yearly injections of inclisiran (after initial doses at days 1 and 90) approximately halved LDL-C levels in patients with, or at high risk of developing, atherosclerotic cardiovascular disease (ASCVD) who had hypercholesterolemia, irrespective of whether or not their existing treatment included a statin. The safety and tolerability profile of the drug was similar to placebo, although mild to moderate, transient injection-site adverse reactions were more frequent with inclisiran. Pending confirmation of the expected reduction in cardiovascular (CV) events with inclisiran, it is a valuable additional/alternative antihyperlipidemic agent to a statin, as its infrequent maintenance dosing regimen confers a convenience advantage over other non-statin LLTs.

摘要

英克西兰(Leqvio)是一种一流的皮下注射小干扰RNA(siRNA),可阻止肝脏合成前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9),从而降低循环中的低密度脂蛋白胆固醇(LDL-C)。在欧盟,英克西兰适用于患有原发性高胆固醇血症或混合性血脂异常的成年人,作为饮食的辅助治疗。它适用于在最大耐受剂量他汀类药物治疗下仍无法达到LDL-C目标的患者,无论是否使用其他降脂疗法(LLT)。对于他汀类药物不耐受或禁忌使用他汀类药物的患者,可联合或不联合其他LLT使用。在临床试验中,对于患有高胆固醇血症、有动脉粥样硬化性心血管疾病(ASCVD)或有发展为ASCVD高风险的患者,每年注射两次英克西兰(在第1天和第90天给予初始剂量后)可使LDL-C水平降低约一半,无论其现有治疗是否包括他汀类药物。该药物的安全性和耐受性与安慰剂相似,尽管英克西兰更常出现轻度至中度的短暂注射部位不良反应。在英克西兰预期的心血管(CV)事件减少得到证实之前,它是他汀类药物一种有价值的额外/替代降血脂药物,因为其不频繁的维持给药方案比其他非他汀类LLT具有便利性优势。

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