Alirocumab and Cardiovascular Outcomes in Patients With Previous Myocardial Infarction: Prespecified Subanalysis From ODYSSEY OUTCOMES.


Journal

The Canadian journal of cardiology
ISSN: 1916-7075
Titre abrégé: Can J Cardiol
Pays: England
ID NLM: 8510280

Informations de publication

Date de publication:
10 2022
Historique:
received: 04 05 2022
revised: 17 05 2022
accepted: 22 05 2022
pubmed: 2 6 2022
medline: 12 10 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

After acute coronary syndrome (ACS), patients with a previous myocardial infarction (MI) may be at particularly high risk for major adverse cardiovascular events (MACE) and death. We studied the effects of the PCSK9 inhibitor alirocumab in patients with recent ACS according to previous history of MI. The ODYSSEY OUTCOMES trial compared alirocumab with placebo, beginning 1 to 12 months after ACS with median 2.8-year follow-up. The primary MACE outcome comprised death from coronary heart disease, nonfatal MI, fatal or nonfatal ischemic stroke, and hospitalization for unstable angina. Of 18,924 patients, 3633 (19.2%) had previous MI. Patients with previous MI were older, more likely male, with more cardiovascular risk factors and previous events. With placebo, 4-year risks of MACE and death were higher among those with vs without previous MI (20.5% vs 8.9%, P < 0.001; 7.4% vs 3.4%, P < 0.001, respectively). Alirocumab reduced the risk of events regardless of the presence or absence of a history of MI (MACE, adjusted hazard ratio [aHR] 0.90, 95% confidence interval [CI], 0.78-1.05 vs 0.82, 0.73-0.92; P A previous history of MI places patients with recent ACS at high risk for recurrent MACE and death. Alirocumab reduced the relative risks of these events consistently in patients with or without previous MI but with numerically greater absolute benefit in the former subgroup. (ODYSSEY OUTCOMES: NCT01663402).

Sections du résumé

BACKGROUND
After acute coronary syndrome (ACS), patients with a previous myocardial infarction (MI) may be at particularly high risk for major adverse cardiovascular events (MACE) and death. We studied the effects of the PCSK9 inhibitor alirocumab in patients with recent ACS according to previous history of MI.
METHODS
The ODYSSEY OUTCOMES trial compared alirocumab with placebo, beginning 1 to 12 months after ACS with median 2.8-year follow-up. The primary MACE outcome comprised death from coronary heart disease, nonfatal MI, fatal or nonfatal ischemic stroke, and hospitalization for unstable angina. Of 18,924 patients, 3633 (19.2%) had previous MI.
RESULTS
Patients with previous MI were older, more likely male, with more cardiovascular risk factors and previous events. With placebo, 4-year risks of MACE and death were higher among those with vs without previous MI (20.5% vs 8.9%, P < 0.001; 7.4% vs 3.4%, P < 0.001, respectively). Alirocumab reduced the risk of events regardless of the presence or absence of a history of MI (MACE, adjusted hazard ratio [aHR] 0.90, 95% confidence interval [CI], 0.78-1.05 vs 0.82, 0.73-0.92; P
CONCLUSIONS
A previous history of MI places patients with recent ACS at high risk for recurrent MACE and death. Alirocumab reduced the relative risks of these events consistently in patients with or without previous MI but with numerically greater absolute benefit in the former subgroup. (ODYSSEY OUTCOMES: NCT01663402).

Identifiants

pubmed: 35644332
pii: S0828-282X(22)00337-3
doi: 10.1016/j.cjca.2022.05.021
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
PCSK9 protein, human EC 3.4.21.-
Proprotein Convertase 9 EC 3.4.21.-
alirocumab PP0SHH6V16

Banques de données

ClinicalTrials.gov
['NCT01663402']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1542-1549

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Chern-En Chiang (CE)

General Clinical Research Center, Division of Cardiology, Taipei Veterans General Hospital and National Yang Ming Chiao Tung University, Taipei, Taiwan. Electronic address: cechiang@vghtpe.gov.tw.

Gregory G Schwartz (GG)

University of Colorado School of Medicine, Aurora, Colorado, USA.

Yedid Elbez (Y)

Deepscover, Puteaux, France.

Michael Szarek (M)

State University of New York, Downstate School of Public Health, Brooklyn, New York, USA; CPC Clinical Research and Division of Cardiology, University of Colorado School of Medicine, Aurora, Colorado, USA.

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart & Vascular Center, Boston, Massachusetts, USA; Harvard Medical School, Boston, Massachusetts, USA.

Vera A Bittner (VA)

Division of Cardiovascular Disease, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Rafael Diaz (R)

Estudios Cardiológicos Latino América, Instituto Cardiovascular de Rosario, Rosario, Argentina.

Andrejs Erglis (A)

Pauls Stradins Clinical University Hospital, University of Latvia, Riga, Latvia.

Shaun G Goodman (SG)

St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada; Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.

Emil Hagström (E)

Department of Medical Sciences, and Uppsala Clinical Research Centre, Uppsala University, Uppsala, Sweden.

J Wouter Jukema (JW)

Department of Cardiology, Leiden University Medical Center, Leiden, The Netherlands.

Evangelos Liberopoulos (E)

Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, Greece.

Megan Loy (M)

Sanofi, Bridgewater Township, New Jersey, USA.

Robert Pordy (R)

Regeneron Pharmaceuticals, Tarrytown, New York, USA.

Harvey D White (HD)

Green Lane Cardiovascular Services, Auckland City Hospital, Auckland, New Zealand.

Tabassome Simon (T)

Sorbonne Université, Assistance Publique-Hôpitaux de Paris, Hôpital Saint Antoine, Paris, France.

Philippe Gabriel Steg (PG)

Department of Cardiology, Université de Paris, Paris, France; Assistance Publique-Hôpitaux de Paris, Hôpital Bichat, Paris, France; FACT (French Alliance for Cardiovascular Trials), Paris, France; INSERM U1148, Paris, France; Imperial College, Royal Brompton Hospital, London, United Kingdom.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH