Key result
PERFECT II trial tests whether early alirocumab improves myocardial salvage index in STEMI.
Why the study?
Effective therapy to attenuate local inflammation after myocardial infarction in patients with STEMI is lacking, and PCSK9 inhibitors may reduce inflammation and improve myocardial salvage and remodeling.
RCT (n=160)
Open-label
1:1 ratio via interactive web response system, stratified by age, gender, and time from symptom onset
Yes
Trial results may inform early PCSK9 use in STEMI; leaves open whether alirocumab improves myocardial salvage.
Background and aims: Primary percutaneous coronary intervention (PPCI) is the most effective treatment strategy for ST-segment elevation myocardial infarction (STEMI). Nevertheless, dysregulated inflammation induced by myocardial reperfusion injury may increase the final infarct size and induce maladaptive myocardial remodeling. Proprotein convertase subtilisin/kexin 9 (PCSK9) inhibitor, as a novel and potent lipid-lowering drug, plays an important role in inflammation. The aim of this study is to investigate whether the early application of PCSK9 inhibitor can increase the myocardial salvage index (MSI) and improve ventricular remodeling in patients with STEMI. Design: the interactive web response system, at a 1:1 ratio. In the PCSK9 inhibitor group, the PCSK9 inhibitor alirocumab at a dose of 75 mg will be subcutaneously injected immediately after PPCI and administered every 2 weeks thereafter for 3 months based on conventional treatment. In the control group, conventional treatment will be administered. The primary endpoint is MSI, as measured by cardiac magnetic resonance imaging (CMR) at 1 week after PPCI. The secondary endpoints are the peak time of creatine kinase (CK)-MB and troponin I (TnI)/TnT after PPCI; the postoperative fall time of the ST segment on electrocardiography (ECG); the rate of plasma low-density lipoprotein cholesterol (LDL-C) compliance (< 1.4 mmol/L and a reduction of >50% from baseline) at 1, 3, and 6 months after PPCI; infarct size and ejection fraction (EF) measured by CMR at 6 months after PPCI; the occurrence of major adverse cardiovascular event (MACE: a composite of cardiovascular death, non-fatal myocardial infarction, stent thrombosis, repeat revascularization, stroke, and heart failure needed to be hospitalized). Conclusions: This is the first multicenter study to investigate the effect of early application of the PCSK9 inhibitor alirocumab on MSI in patients with STEMI undergoing PPCI. The findings will provide an opportunity to explore novel ideas and methods for the treatment of acute myocardial infarction. Trial registration: ClinicalTrials.gov, identifier: NCT05292404.
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Xia et al. (2022) conducted an RCT in ST-segment elevation myocardial infarction (STEMI) (n=160). Alirocumab vs. Conventional treatment was evaluated on Myocardial salvage index (MSI) measured by cardiac magnetic resonance imaging (CMR) at 1 week after PPCI. The PERFECT II trial is a planned multicenter, open-label randomized controlled trial designed to evaluate whether early administration of the PCSK9 inhibitor alirocumab improves the myocardial salvage index in patients with STEMI.
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