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Effects of alirocumab on types of myocardial infarction: Insights from the ODYSSEY OUTCOMES trial

  • ODYSSEY OUTCOMES Investigators
  • Auckland District Health Board
  • Université Paris Cité
  • Royal Brompton and Harefield NHS Foundation Trust
  • SUNY Downstate Health Sciences University
  • Harvard University
  • University of Alabama at Birmingham
  • Instituto Cardiovascular de Rosario
  • Sanofi-Aventis
  • Paula Stradina Clinical University Hospital
  • University of Alberta
  • University of Toronto
  • Stanford University
  • Leiden University
  • Duke University
  • Regeneron Pharmaceuticals, Inc.
  • Mahidol University
  • CSL Behring
  • Goethe University Frankfurt
  • University of Colorado Anschutz Medical Campus

Research output: Contribution to journalArticlepeer-review

54 Citations (Scopus)

Abstract

Aims The third Universal Definition of Myocardial Infarction (MI) Task Force classified MIs into five types: Type 1, spontaneous; Type 2, related to oxygen supply/demand imbalance; Type 3, fatal without ascertainment of cardiac biomarkers; Type 4, related to percutaneous coronary intervention; and Type 5, related to coronary artery bypass surgery. Low-density lipoprotein cholesterol (LDL-C) reduction with statins and proprotein convertase subtilisin–kexin Type 9 (PCSK9) inhibitors reduces risk of MI, but less is known about effects on types of MI. ODYSSEY OUTCOMES compared the PCSK9 inhibitor alirocumab with placebo in 18 924 patients with recent acute coronary syndrome (ACS) and elevated LDL-C (≥1.8 mmol/L) despite intensive statin therapy. In a pre-specified analysis, we assessed the effects of alirocumab on types of MI. Methods and results Median follow-up was 2.8 years. Myocardial infarction types were prospectively adjudicated and classified. Of 1860 total MIs, 1223 (65.8%) were adjudicated as Type 1, 386 (20.8%) as Type 2, and 244 (13.1%) as Type 4. Few events were Type 3 (n = 2) or Type 5 (n = 5). Alirocumab reduced first MIs [hazard ratio (HR) 0.85, 95% confidence interval (CI) 0.77–0.95; P = 0.003], with reductions in both Type 1 (HR 0.87, 95% CI 0.77–0.99; P = 0.032) and Type 2 (0.77, 0.61–0.97; P = 0.025), but not Type 4 MI.

Original languageEnglish
Pages (from-to)2801-2809
Number of pages9
JournalEuropean Heart Journal
Volume40
Issue number33
DOIs
Publication statusPublished - 1 Sept 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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