PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia

被引:37
作者
Ito, Matthew K. [1 ,2 ]
Santos, Raul D. [3 ,4 ,5 ]
机构
[1] Sanofi US, 55 Corp Dr, Bridgewater, NJ 08807 USA
[2] Oregon Hlth & Sci Univ, Oregon State Univ, Coll Pharm, Portland, OR 97201 USA
[3] Univ Sao Paulo, Med Sch Hosp, Heart Inst InCor, Lipid Clin, Sao Paulo, Brazil
[4] Hosp Israelita Albert Einstein, Prevent Med Ctr, Sao Paulo, Brazil
[5] Hosp Israelita Albert Einstein, Cardiol Program, Sao Paulo, Brazil
关键词
alirocumab; bococizumab; evolocumab; hyperlipidemia; low-density lipoprotein cholesterol; proprotein convertase subtilisin; kexin type 9; SUBTILISIN/KEXIN TYPE 9; DENSITY-LIPOPROTEIN CHOLESTEROL; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; CARDIOVASCULAR-RISK PATIENTS; EVOLOCUMAB AMG 145; LIPID ASSOCIATION RECOMMENDATIONS; PATIENT-CENTERED MANAGEMENT; STATIN-INTOLERANT PATIENTS; DOUBLE-BLIND; LDL-C;
D O I
10.1002/jcph.766
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Current guidelines for hypercholesterolemia treatment emphasize lifestyle modification and lipid-modifying therapy to reduce the risk for cardiovascular disease. Statins are the primary class of agents used for the treatment of hypercholesterolemia. Although statins are effective for many patients, they fail to achieve optimal reduction in lipids for some patients, including those who have or are at high risk for cardiovascular disease. The PCSK9 gene was identified in the past decade as a potential therapeutic target for the management of patients with hypercholesterolemia. Pharmacologic interventions to decrease PCSK9 levels are in development, with the most promising approach using monoclonal antibodies that bind to PCSK9 in the plasma. Two monoclonal antibodies, alirocumab and evolocumab, have recently been approved for the treatment of hypercholesterolemia, and a third one, bococizumab, is in phase 3 clinical development. All 3 agents achieve significant reductions in levels of low-density lipoprotein cholesterol, as well as reductions in non-high-density lipoprotein cholesterol, apolipoprotein B, and lipoprotein(a). Long-term outcome trials are under way to determine the sustained efficacy, safety, and tolerability of PCSK9 inhibitors and whether this novel class of agents decreases the risk for major cardiovascular events in patients on lipid-modifying therapy. Available data suggest that PCSK9 inhibitors provide a robust reduction in atherogenic cholesterol levels with a good safety profile, especially for patients who fail to obtain an optimal clinical response to statin therapy, those who are statin intolerant or have contraindications to statin therapy, and those with familial hypercholesterolemia.
引用
收藏
页码:7 / 32
页数:26
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