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佩拉卡森的临床药理学评价:一种降低脂蛋白(a)的药物。

A Review of the Clinical Pharmacology of Pelacarsen: A Lipoprotein(a)-Lowering Agent.

机构信息

East Coast Institute for Research, Jacksonville, FL, USA.

Ashchi Heart and Vascular Center, Jacksonville, FL, USA.

出版信息

Am J Cardiovasc Drugs. 2022 Jan;22(1):47-54. doi: 10.1007/s40256-021-00499-1. Epub 2021 Sep 7.


DOI:10.1007/s40256-021-00499-1
PMID:34490591
Abstract

Patients with genetically associated elevated lipoprotein(a) [Lp(a)] levels are at greater risk for coronary artery disease, heart attack, stroke, and peripheral arterial disease. To date, there are no US FDA-approved drug therapies that are designed to target Lp(a) with the goal of lowering the Lp(a) level in patients who have increased risk. The American College of Cardiology (ACC) has provided guidelines on how to use traditional lipid profiles to assess the risk of atherosclerotic cardiovascular disease (ASCVD); however, even with the emergence of statin add-on therapies such as ezetimibe and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, some populations with elevated Lp(a) biomarkers remain at an increased risk for cardiovascular (CV) disease. Residual CV risk has led researchers to inquire about how lowering Lp(a) can be used as a potential preventative therapy in reducing CV events. This review aims to present and discuss the current clinical and scientific evidence pertaining to pelacarsen.

摘要

脂蛋白(a) [Lp(a)]水平升高与遗传有关的患者发生冠状动脉疾病、心脏病发作、中风和外周动脉疾病的风险更高。迄今为止,尚无美国食品和药物管理局 (FDA) 批准的专门针对 Lp(a) 的药物疗法,旨在降低有风险升高的患者的 Lp(a)水平。美国心脏病学会 (ACC) 已就如何使用传统脂质谱来评估动脉粥样硬化性心血管疾病 (ASCVD) 的风险提供了指南;然而,即使出现了依折麦布和前蛋白转化酶枯草溶菌素 9 (PCSK9) 抑制剂等他汀类药物的附加疗法,一些 Lp(a) 生物标志物升高的人群仍然存在心血管 (CV) 疾病的风险增加。残余 CV 风险促使研究人员询问降低 Lp(a) 如何用作降低 CV 事件的潜在预防疗法。本综述旨在介绍和讨论与 pelacarsen 相关的当前临床和科学证据。

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[1]
Advances in Non-statin Lipid Therapies: A Narrative Review of Evolving Strategies for Cardiovascular Risk Reduction.

Am J Cardiovasc Drugs. 2025-8-30

[2]
Non-traditional lipid biomarkers in atherosclerotic cardiovascular disease: pathophysiological mechanisms and strategies to address residual risk.

Front Endocrinol (Lausanne). 2025-7-10

[3]
Hepatocyte targeting the asialoglycoprotein receptor.

RSC Med Chem. 2024-12-2

[4]
Role of Lipoprotein(a) Reduction in Cardiovascular Disease.

J Clin Med. 2024-10-22

[5]
Lipids and Inflammation: Novel Molecular Targets and Therapeutic Implications.

Curr Med Chem. 2024-9-16

[6]
Targeting Lipoprotein(a): Can RNA Therapeutics Provide the Next Step in the Prevention of Cardiovascular Disease?

Cardiol Ther. 2024-3

[7]
Molecular Therapies in Cardiovascular Diseases: Small Interfering RNA in Atherosclerosis, Heart Failure, and Hypertension.

Int J Mol Sci. 2023-12-26

[8]
Atherogenic Dyslipidemias: Unmet Needs and the Therapeutic Potential of Emerging and Novel Approaches and Drugs.

Pharmaceuticals (Basel). 2023-1-24

[9]
Lipoprotein(a) As a Risk Factor in a Cohort of Hospitalised Cardiovascular Patients: A Retrospective Clinical Routine Data Analysis.

J Clin Med. 2023-4-29

[10]
Using genetic association data to guide drug discovery and development: Review of methods and applications.

Am J Hum Genet. 2023-2-2

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