Lipid-Modifying Agents, From Statins to PCSK9 Inhibitors: JACC Focus Seminar

J Am Coll Cardiol. 2020 Apr 28;75(16):1945-1955. doi: 10.1016/j.jacc.2019.11.072.

Abstract

Mendelian randomization studies and randomized trials have conclusively demonstrated that lower low-density lipoprotein (LDL) cholesterol results in fewer cardiovascular events. This review describes key stages in the evolution of LDL cholesterol-lowering treatment. Data from over 25 cardiovascular outcome trials confirm that, within a few years, statins lower the relative risk of major atherosclerotic events by about 22% per 38.7 mg/dl (1 mmol/l) reduction in LDL cholesterol, with similar benefit across patient subgroups. Meta-analyses of these trials have established the safety of statins with regard to nonvascular mortality and cancer. Other agents available for prescription include ezetimibe and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, which both reduce major atherosclerotic events in proportion to their effects on LDL cholesterol and have good safety profiles, though PCSK9 inhibitors remain costly. Investigational LDL cholesterol-lowering agents currently being tested in cardiovascular outcome studies are bempedoic acid, an adenosine triphosphate-citrate lyase inhibitor that reduces cholesterol synthesis, and inclisiran, a double-stranded small interfering ribonucleic acid that inhibits PCSK9 synthesis.

Keywords: Mendelian randomization; cardiovascular; ezetimibe; low-density lipoprotein cholesterol; proprotein convertase subtilisin/kexin type 9; statin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anticholesteremic Agents* / classification
  • Anticholesteremic Agents* / pharmacology
  • Cardiovascular Diseases* / metabolism
  • Cardiovascular Diseases* / prevention & control
  • Cholesterol, LDL / metabolism*
  • Humans
  • Mendelian Randomization Analysis

Substances

  • Anticholesteremic Agents
  • Cholesterol, LDL