Impact of Alirocumab on Release Markers of Atherosclerotic Plaque Vulnerability in Patients with Mixed Hyperlipidemia and Vulnerable Atherosclerotic Plaque

Medicina (Kaunas). 2022 Jul 21;58(7):969. doi: 10.3390/medicina58070969.

Abstract

Background and Objectives: Atherosclerosis is a disease in the pathogenesis of which plasma factors apart from elevated cholesterol levels play a keyrole. Such factors include osteopontin (OPN), osteoprotegerin (OPG), and metalloproteinases (MMPs), which are factors that may be responsible for the stabilization of atherosclerotic plaque. The aim of this study was to assess the effect of modern lipid-lowering therapy by using proprotein convertase subtilisin/kexin type 9 (PCSK-9) inhibitor on the concentrations of these factors. Materials and Methods: The study included people suffering from dyslipidemia who were eligible to start alirocumab therapy. In this group, the concentrations of OPN, OPG, and MMPs were assessed before the initiation of therapy and after three months of its duration. Results: In the study, we observed a statistically significant reduction in the concentrations of OPN, OPG (p < 0.001), and metalloproteinase 2 (MMP-2) (p < 0.05) after the applied therapy. Moreover, we noticed that in the group of patients soon to start alirocumab therapy, the concentrations of these factors were higher compared to the control group (p < 0.001). Conclusions: The results of our study show that therapy with alirocumab significantly reduces the concentration of factors that affect atherosclerotic plaque vulnerability, which may explain their important role in reducing cardiovascular risk in patients undergoing this therapy.

Keywords: PCSK-9 inhibitors; atherosclerotic plaque; dyslipidemia; metalloproteinase 2; metalloproteinase 9; osteopontin; osteoprotegerin.

MeSH terms

  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Biomarkers
  • Humans
  • Hyperlipidemias*
  • Matrix Metalloproteinase 2
  • Plaque, Atherosclerotic* / drug therapy

Substances

  • Antibodies, Monoclonal, Humanized
  • Biomarkers
  • Matrix Metalloproteinase 2
  • alirocumab