Journal
TRENDS IN CARDIOVASCULAR MEDICINE
Volume 30, Issue 3, Pages 179-185Publisher
ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tcm.2019.05.007
Keywords
Proprotein Convertase Subtilisin/Kexin Type 9 inhibitors; Dysiipidemia; Lipid lowering therapy
Categories
Funding
- NIH [K12 HD043488]
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Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) has revolutionized our understanding of cholesterol homeostasis and added to our arsenal against atherosclerotic cardiovascular disease (ASCVD). In a span of approximately 15 years, PCSK9 has morphed from an esoteric and rare cause of familial hypercholesterolemia (FH) into the most efficient cholesterol-lowering target ever known, with the completion of two large scale cardiovascular outcome trials showing positive results. Current Food and Drug Administration (FDA) approved modalities to inhibit PCSK9 are in the form of monoclonal antibodies which display an unparalleled degree of low-density lipoprotein cholesterol (LDL-C) lowering and expand upon the notion that lower LDL-C is better for ASCVD risk reduction. However, the accelerated pace of discovery and therapeutic development has left large gaps in our knowledge regarding the physiology and function of PCSK9. The aim of this review is to provide context to the discovery, history, treatment and current status of PCSK9 and its therapeutic inhibitors and highlight areas of controversy and future directions. (C) 2019 The Authors. Published by Elsevier Inc.
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