Alirocumab in lipoprotein apheresis: A synergy for patients with high-Lp(a)

Transfus Apher Sci. 2023 Jun;62(3):103660. doi: 10.1016/j.transci.2023.103660. Epub 2023 Feb 21.

Abstract

Until today lipoprotein apheresis (LA) is considered the most effective treatment for patients with high-Lp(a) and proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) are often combined with LA to dampen the rebound in lipoprotein concentrations. The aim of the present work is to evaluate the effect of dose-adjustment strategy for alirocumab in a small cohort of high-Lp(a) subjects with ischemic heart disease and in chronic LA treatment. Chronic LA effect on Lp(a) levels is a significant reduction in pre-LA Lp(a) concentrations compared to native Lp(a) value (118 [116-119] mg/dl vs 150 [137-155] mg/dl; p < 0.001). Furthermore, the administration of Arilocumab 75 mg after 7 days from LA shows a significant pre-LA reduction in the Lp(a) concentrations respect to those obtained with administration immediately after the LA treatment. In high-Lp(a) patients treated with chronic LA the deferred addition of alirocumab, resulted in lower LDL-cholesterol and Lp(a) values.

Keywords: Alirocumab; Hyper-Lp (a); Lipoprotein apheresis; PCSK9 inhibitors.

MeSH terms

  • Antibodies, Monoclonal, Humanized / pharmacology
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Blood Component Removal* / methods
  • Humans
  • Lipoprotein(a)
  • PCSK9 Inhibitors*
  • Treatment Outcome

Substances

  • alirocumab
  • PCSK9 Inhibitors
  • Antibodies, Monoclonal, Humanized
  • Lipoprotein(a)