Role of PCSK9 in lipid metabolism and atherosclerosis

Biomed Pharmacother. 2018 Aug:104:36-44. doi: 10.1016/j.biopha.2018.05.024. Epub 2018 May 11.

Abstract

Elevated plasma low-density lipoprotein cholesterol (LDL-C) is an important risk factor for cardiovascular diseases. Statins are the most widely used therapy for patients with hyperlipidemia. However, a significant residual cardiovascular risk remains in some patients even after maximally tolerated statin therapy. Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a new pharmacologically therapeutic target for decreasing LDL-C. PCSK9 reduces LDL intake from circulation by enhancing LDLR degradation and preventing LDLR recirculation to the cell surface. Moreover, PCSK9 inhibitors have been approved for patients with either familial hypercholesterolemia or atherosclerotic cardiovascular disease, who require additional reduction of LDL-C. In addition, PCSK9 inhibition combined with statins has been used as a new approach to help reduce LDL-C levels in patients with either statin intolerance or unattainable LDL goal. This review will discuss the emerging anti-PCSK9 therapies in the regulation of cholesterol metabolism and atherosclerosis.

Keywords: Cholesterol; Lipoprotein receptors; Low density lipoprotein; Proprotein convertase subtilisin/kexin type 9.

Publication types

  • Review

MeSH terms

  • Animals
  • Anticholesteremic Agents / pharmacology
  • Anticholesteremic Agents / therapeutic use
  • Atherosclerosis / drug therapy
  • Atherosclerosis / metabolism*
  • Cholesterol, LDL / metabolism
  • Humans
  • Hypercholesterolemia / drug therapy
  • Hypercholesterolemia / metabolism
  • Lipid Metabolism / drug effects
  • Lipid Metabolism / physiology*
  • Proprotein Convertase 9 / metabolism*

Substances

  • Anticholesteremic Agents
  • Cholesterol, LDL
  • Proprotein Convertase 9