Coronary disease & ACS

Platelet activation and endothelial dysfunction biomarkers in acute coronary syndrome: the impact of PCSK9 inhibition

Eur Heart J Cardiovasc PharmacotherPublished Randomised controlled trial with mechanistic tissue substudy

Authors' conclusion

Proprotein Convertase Subtilisin/Kexin 9 inhibition decreases markers of platelet activation and endothelial dysfunction in ACS patients. PCSK9 is associated with platelets and vascular ECs in LIMA segments and PCSK9 inhibition decreases that interaction.

Study context

Population
Acute coronary syndromes (ACS) patients enrolled in the Evolocumab in ACS trials12 with left internal mammary artery (LIMA) specimens
Participants
46 patients
Comparison
Evolocumab vs placebo
Primary endpoint
Platelet activation markers (PF4, P-selectin) and endothelial dysfunction marker (vWF)
Follow-up
30 days
Methodological detailsplacebo-controlled
  • Placebo-controlled

Primary result

As reported in the abstract

PF4, P-selectin and vWF (controlling for baseline)
  • PF4 and von Willebrand factor (vWF) significantly lower with evolocumab than placebo

Further findings

LIMA immunostaining (PCSK9, CD61, CD31)

Colocalization of PCSK9, CD61 and CD31 at the vascular endothelium
Evolocumab associated with decreased overlap of PCSK9, CD61 and CD31

Original publication

Platelet activation and endothelial dysfunction biomarkers in acute coronary syndrome: the impact of PCSK9 inhibition. Eur Heart J Cardiovasc Pharmacother. Published 19 July 2023. doi:10.1093/ehjcvp/pvad051

Summarised from the published abstract; every number is checked against it

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