Therapeutic Agents Targeting Cardiometabolic Risk for Preventing and Treating Atherosclerotic Cardiovascular Diseases

被引:12
|
作者
Arsenault, Benoit J. [1 ,2 ]
Perrot, Nicolas [1 ,2 ]
Puri, Rishi [3 ,4 ]
机构
[1] Inst Univ Cardiol & Pneumol Quebec, Ctr Rech, Quebec City, PQ, Canada
[2] Univ Laval, Fac Med, Dept Med, Quebec City, PQ, Canada
[3] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44106 USA
[4] Univ Adelaide, Dept Med, Adelaide, SA, Australia
基金
加拿大健康研究院;
关键词
CORONARY-ARTERY-DISEASE; KEXIN TYPE 9; STATIN THERAPY; DOUBLE-BLIND; MYOCARDIAL-INFARCTION; SECONDARY ANALYSIS; CONTROLLED-TRIAL; LOW LDL; CHOLESTEROL; EVENTS;
D O I
10.1002/cpt.1110
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Targeting atherogenic lipoprotein levels with statins remains the current cornerstone of atherosclerotic cardiovascular disease (ACVD) management. In patients at high ACVD risk who cannot achieve the desired low-density lipoprotein (LDL) cholesterol target, the addition of compounds such as ezetimibe and proprotein subtilisin/kexin type-9 (PCSK9) inhibitors incrementally lowers cardiovascular risk. New glucose-lowering drugs such as glucacon-like peptide-1 receptor (GLP1R) agonists and sodium-glucose cotransporter-2 (SGLT2) inhibitors were also shown to improve cardiometabolic risk factors and provide cardiovascular benefits in patients with type 2 diabetes. Our objective is to review the role of these agents in the management of patients at high ACVD risk and introduce new and (re)-emerging drugs targeting atherogenic lipoproteins such as LDL (inclisiran, bempedoic acid, etc.), remnant-like particles (fibrates, volanesorsen, and angiopoietin-like protein-3 (ANGPTL3) inhibitors), and lipoprotein(a) (AKCEA-APO[A]L-RX). The potential role of drugs targeting inflammation (canakinumab, methotrexate, and colchicine) in ACVD risk prevention/management will also be discussed.
引用
收藏
页码:257 / 268
页数:12
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