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依洛尤单抗:降低 LDL-C 水平和预防动脉粥样硬化性心血管疾病的新策略。

Inclisiran: A New Strategy for LDL-C Lowering and Prevention of Atherosclerotic Cardiovascular Disease.

机构信息

Internal Medicine Department, University of Miami Miller School of Medicine/ Jackson Memorial Hospital, Miami, FL, USA.

Ciccarone Center for the Prevention of Cardiovascular Disease, Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Vasc Health Risk Manag. 2023 Jul 6;19:421-431. doi: 10.2147/VHRM.S338424. eCollection 2023.

Abstract

Multiple lines of evidence confirm that the cumulative burden of low-density lipoprotein cholesterol (LDL-C) is causally related to the development of atherosclerotic cardiovascular disease (ASCVD). As such, lowering LDL-C is a central tenet in all ASCVD prevention guidelines, which recommend matching the intensity of LDL-C lowering with the absolute risk of the patient. Unfortunately, issues such as difficulty with long-term adherence to statin therapy and inability to achieve desired LDL-C thresholds with statins alone results in residual elevated ASCVD risk. Non-statin therapies generally provide similar risk reduction per mmol/L of LDL-C reduction and are included by major society guidelines as part of the treatment algorithm for managing LDL-C. Per the 2022 American College of Cardiology Expert Consensus Decision Pathway, patients with ASCVD are recommended to achieve both an LDL-C reduction ≥50% and an LDL-C threshold of <55 mg/dL in patients at very high-risk and <70 mg/dL in those not at very high risk. Patients with familial hypercholesterolemia (FH) but without ASCVD should lower LDL-C to <100 mg/dL. For patients who remain above LDL-C thresholds with maximally tolerated statin therapy plus lifestyle changes, non-statin therapy warrants strong consideration. While several non-statin therapies have been granted FDA approval for managing hypercholesterolemia (eg, ezetimibe, Proprotein Convertase Subtilisin/Kexin 9 [PCSK9] monoclonal antibodies, and bempedoic acid), the focus of the current review is on inclisiran, a novel small interfering RNA therapy that inhibits the production of the PCSK9 protein. Inclisiran is currently FDA approved as an adjunct to statin therapy in patients with clinical ASCVD or heterozygous FH who require additional LDL-lowering. The drug is administered by subcutaneous injection twice a year, after an initial baseline and 3 month dose. In this review, we sought to provide an overview of the use of inclisiran, review current trial data, and outline an approach to potential patient selection.

摘要

大量证据证实,低密度脂蛋白胆固醇(LDL-C)的累积负担与动脉粥样硬化性心血管疾病(ASCVD)的发生有因果关系。因此,降低 LDL-C 是所有 ASCVD 预防指南的核心原则,这些指南建议根据患者的绝对风险来匹配 LDL-C 降低的强度。不幸的是,由于他汀类药物治疗的长期依从性困难以及单独使用他汀类药物无法达到理想的 LDL-C 阈值等问题,导致 ASCVD 的残余风险仍然较高。非他汀类药物治疗通常可提供每降低 1mmol/L LDL-C 相似的风险降低,并且被主要学会指南作为管理 LDL-C 治疗方案的一部分纳入。根据 2022 年美国心脏病学会专家共识决策途径,建议 ASCVD 患者在极高危患者中实现 LDL-C 降低≥50%和 LDL-C 阈值<55mg/dL,以及非极高危患者中 LDL-C 阈值<70mg/dL。无 ASCVD 的家族性高胆固醇血症(FH)患者应将 LDL-C 降低至<100mg/dL。对于那些在最大耐受剂量他汀类药物联合生活方式改变后仍处于 LDL-C 阈值以上的患者,应强烈考虑非他汀类药物治疗。虽然几种非他汀类药物已获得 FDA 批准用于治疗高胆固醇血症(例如依折麦布、前蛋白转化酶枯草溶菌素 9[PCSK9]单克隆抗体和贝匹莫德酸),但目前的综述重点是inclisiran,一种新型的小干扰 RNA 治疗药物,可抑制 PCSK9 蛋白的产生。Inclisiran 目前被 FDA 批准作为他汀类药物的辅助药物,用于需要进一步降低 LDL-C 的有临床 ASCVD 或杂合子 FH 的患者。该药通过皮下注射给药,每 6 个月给药 2 次,初始剂量为基线剂量和 3 个月剂量。在本综述中,我们旨在提供 inclisiran 使用的概述,回顾当前的试验数据,并概述潜在患者选择的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6de/10332363/0b98510a3217/VHRM-19-421-g0001.jpg

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