Modulation of microRNAs by aspirin in cardiovascular disease

Trends Cardiovasc Med. 2020 Jul;30(5):249-254. doi: 10.1016/j.tcm.2019.08.005. Epub 2019 Aug 14.

Abstract

Aspirin is among the most widely prescribed drugs in cardiovascular and cerebrovascular diseases for both primary and secondary prevention. The major mechanisms underlying its benefits are the inhibitory effects on platelet activation and prostanoid biosynthesis induced by COX-1 and COX-2 inactivation. MicroRNAs (miRNAs) are newly proposed mediators of the effects of aspirin. In this review, we summarize the evidence on the links between miRNAs and aspirin use in relation to cardiovascular diseases. In addition, we discuss the studies suggesting a possible role for miRNAs as biomarkers of aspirin resistance, a condition during which atherothrombotic events occur despite aspirin use, and which affects a considerable proportion of patients with cardiovascular disease.

Keywords: Aspirin; Aspirin resistance; Cardiovascular disease; MicroRNA; Thrombosis.

Publication types

  • Review

MeSH terms

  • Animals
  • Aspirin / adverse effects
  • Aspirin / therapeutic use*
  • Blood Platelets / drug effects*
  • Blood Platelets / metabolism
  • Cardiovascular Diseases / drug therapy*
  • Cardiovascular Diseases / genetics
  • Cardiovascular Diseases / metabolism
  • Docosahexaenoic Acids / metabolism
  • Drug Resistance
  • Eicosapentaenoic Acid / metabolism
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Humans
  • Lipoxins / metabolism
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism
  • Platelet Aggregation Inhibitors / adverse effects
  • Platelet Aggregation Inhibitors / therapeutic use*

Substances

  • Lipoxins
  • MicroRNAs
  • Platelet Aggregation Inhibitors
  • Docosahexaenoic Acids
  • Eicosapentaenoic Acid
  • Aspirin