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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

Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

54 Atsauces (Scopus)

Kopsavilkums

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.

OriģinālvalodaAngļu
Lapas (no-līdz)2801-2809
Lapu skaits9
ŽurnālsEuropean Heart Journal
Sējums40
Izdevuma numurs33
DOIs
Publikācijas statussPublicēts - 1 sept. 2019
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