PCSK9 inhibitors for prevention of atherosclerotic cardiovascular disease

被引:11
作者
Bittner, Vera A. [1 ]
Giugliano, Robert P. [2 ]
Brinton, Eliot A. [3 ]
Guyton, John R. [4 ]
机构
[1] Univ Alabama Birmingham, Div Cardiovasc Dis, Birmingham, AL 35294 USA
[2] Brigham & Womens Hosp, Div Cardiovasc Med, Thrombolysis Myocardial Infarct TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA
[3] Utah Lipid Ctr, Salt Lake City, UT USA
[4] Duke Univ, Med Ctr, Dept Med, Div Endocrinol Metab & Nutr, Durham, NC 27710 USA
关键词
PCSK9; Evolocumab; Alirocumab; Cardiovascular outcomes; Safety; RANDOMIZED-TRIAL;
D O I
10.1016/j.jacl.2018.06.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The discovery of proprotein convertase subtilisin kexin-type 9 (PCSK9) and the development of inhibitors of PCSK9 function appear to mark an epochal advance in clinical lipidology. PCSK9 is a circulating protein that binds to low-density lipoprotein (LDL) receptors and facilitates their lysosomal degradation following internalization in cells. Blocking PCSK9 thus increases the recycling of LDL receptors and results in more receptors on the cell surface, particularly in the liver, thereby lowering LDL levels. In this Roundtable, we discuss the recent large cardiovascular outcomes trials in which evolocumab and alirocumab, monoclonal antibodies directed against PCSK9, successfully reduced major cardiovascular events. We discuss the safety of these drugs as well as the safety of maintaining very low LDL cholesterol levels. Finally, we address pragmatic considerations affecting the use of PCSK9 inhibitors in clinical practice. (C) 2018 National Lipid Association. All rights reserved.
引用
收藏
页码:835 / 843
页数:9
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