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Effects of the PCSK9 antibody alirocumab on coronary atherosclerosis in patients with acute myocardial infarction: a serial, multivessel, intravascular ultrasound, near-infrared spectroscopy and optical coherence tomography imaging study-Rationale and design of the PACMAN-AMI trial.

Authors :
Zanchin C
Koskinas KC
Ueki Y
Losdat S
Häner JD
Bär S
Otsuka T
Inderkum A
Jensen MRJ
Lonborg J
Fahrni G
Ondracek AS
Daemen J
van Geuns RJ
Iglesias JF
Matter CM
Spirk D
Juni P
Mach F
Heg D
Engstrom T
Lang I
Windecker S
Räber L
Source :
American heart journal [Am Heart J] 2021 Aug; Vol. 238, pp. 33-44. Date of Electronic Publication: 2021 May 02.
Publication Year :
2021

Abstract

Background: The risk for cardiovascular adverse events after acute myocardial infarction (AMI) remains high despite potent medical treatment including low-density lipoprotein cholesterol (LDL-C) lowering with statins. Proprotein convertase subtilisin/kexin type 9 (PCSK9) antibodies substantially reduce LDL-C when added to statin. Alirocumab, a monoclonal antibody to PCSK9, reduces major adverse cardiovascular events after AMI. The effects of alirocumab on coronary atherosclerosis including plaque burden, plaque composition and fibrous cap thickness in patients presenting with AMI remains unknown.<br />Aims: To determine the effect of LDL-C lowering with alirocumab on top of high-intensity statin therapy on intravascular ultrasound (IVUS)-derived percent atheroma volume (PAV), near-infrared spectroscopy (NIRS)-derived maximum lipid core burden index within 4 mm (maxLCBI <subscript>4 mm</subscript> ) and optical coherence tomography (OCT)-derived fibrous cap thickness (FCT) in patients with AMI.<br />Methods: In this multicenter, double-blind, placebo-controlled trial, 300 patients with AMI (ST-elevation or non-ST-elevation myocardial infarction) were randomly assigned to receive either biweekly subcutaneous alirocumab (150 mg) or placebo beginning <24 hours after the acute event as add-on therapy to rosuvastatin 20 mg. Patients undergo serial IVUS, NIRS and OCT in the two non-infarct related arteries at baseline (at the time of treatment of the culprit lesion) and at 52 weeks. The primary endpoint, change in IVUS-derived PAV, and the powered secondary endpoints, change in NIRS-derived maxLCBI <subscript>4 mm</subscript> , and OCT-derived minimal FCT, will be assessed 52 weeks post randomization.<br />Summary: The PACMAN-AMI trial will determine the effect of alirocumab on top of high-intensity statin therapy on high-risk coronary plaque characteristics as assessed by serial, multimodality intracoronary imaging in patients presenting with AMI.<br />Clinical Trial Registration: NCT03067844.<br /> (Copyright © 2021. Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1097-6744
Volume :
238
Database :
MEDLINE
Journal :
American heart journal
Publication Type :
Academic Journal
Accession number :
33951415
Full Text :
https://doi.org/10.1016/j.ahj.2021.04.006