Genetic Inhibition of PCSK9 and Liver Function

JAMA Cardiol. 2021 Mar 1;6(3):353-354. doi: 10.1001/jamacardio.2020.5341.

Abstract

This study investigates associations of the lifelong genetic inhibition of PCSK9 with plasma liver enzymes and nonalcoholic fatty liver disease by using the loss-of-function variant PCSK9-p.Arg46Leu as a genetic instrument.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Aspartate Aminotransferases / blood
  • Genetic Association Studies
  • Humans
  • Loss of Function Mutation
  • Non-alcoholic Fatty Liver Disease
  • PCSK9 Inhibitors*
  • Proprotein Convertase 9 / genetics*
  • gamma-Glutamyltransferase / blood

Substances

  • PCSK9 Inhibitors
  • gamma-Glutamyltransferase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • PCSK9 protein, human
  • Proprotein Convertase 9