Effect of adding PCSK9 inhibitors to lipid-lowering interventions on arterial stiffness: A systematic review and

I Cavero-Redondo1,2, N Moreno-Herraiz1, A Del Saz-Lara1,3,4

  • 1CarVasCare Research Group (2023-GRIN-34459), Faculta de Enfermería de Cuenca, Universidad de Castilla-La Mancha, Cuenca, Spain.

Insights

Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) significantly improve arterial stiffness beyond lowering LDL-C. This finding suggests broader vascular benefits for cardiovascular health.

Area of Science:

  • Cardiovascular Medicine
  • Pharmacology
  • Vascular Biology

Background:

  • Atherosclerosis management requires controlling hypercholesterolemia, particularly elevated LDL-C.
  • Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) have revolutionized lipid-lowering therapies.
  • Potential pleiotropic effects of PCSK9i on arterial health, beyond lipid reduction, warrant investigation.

Purpose of the Study:

  • To systematically review and meta-analyze the effects of PCSK9i on arterial stiffness.
  • To assess the impact of PCSK9i on vascular health beyond traditional lipid-lowering metrics.
  • To contribute to a comprehensive understanding of cardiovascular risk reduction strategies.

Main Methods:

  • Systematic literature search across databases, trial registries, and grey literature.
  • Inclusion of prospective cohort studies on adults receiving PCSK9i therapy.
  • Analysis of arterial stiffness measured by pulse wave velocity (PWv) using random-effects meta-analyses and meta-regression.

Main Results:

  • Five studies with 158 participants met the criteria.
  • A significant reduction in PWv was observed with PCSK9i addition (mean difference: -2.61 m/s).
  • Subgroup analyses indicated potential variations based on sex and baseline PWv.

Conclusions:

  • Adding PCSK9i to lipid-lowering interventions significantly improves arterial stiffness.
  • PCSK9i demonstrate vascular benefits extending beyond LDL-C reduction.
  • Findings support a broader role for PCSK9i in cardiovascular risk management.
Abstract

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