Reduced Heart Failure and Mortality in Patients Receiving Statin Therapy Before Initial Acute Coronary Syndrome.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
24 05 2022
Historique:
received: 15 10 2021
revised: 09 02 2022
accepted: 10 03 2022
entrez: 19 5 2022
pubmed: 20 5 2022
medline: 24 5 2022
Statut: ppublish

Résumé

There is uncertainty regarding the impact of statins on the risk of atherosclerotic cardiovascular disease (ASCVD) and its major complication, acute heart failure (AHF). The aim of this study was to investigate whether previous statin therapy translates into lower AHF events and improved survival from AHF among patients presenting with an acute coronary syndrome (ACS) as a first manifestation of ASCVD. Data were drawn from the International Survey of Acute Coronary Syndromes Archives. The study participants consisted of 14,542 Caucasian patients presenting with ACS without previous ASCVD events. Statin users before the index event were compared with nonusers by using inverse probability weighting models. Estimates were compared by test of interaction on the log scale. Main outcome measures were the incidence of AHF according to Killip class and the rate of 30-day all-cause mortality in patients presenting with AHF. Previous statin therapy was associated with a significantly decreased rate of AHF on admission (4.3% absolute risk reduction; risk ratio [RR]: 0.72; 95% CI: 0.62-0.83) regardless of younger (40-75 years) or older age (interaction P = 0.27) and sex (interaction P = 0.22). Moreover, previous statin therapy predicted a lower risk of 30-day mortality in the subset of patients presenting with AHF on admission (5.2 % absolute risk reduction; RR: 0.71; 95% CI: 0.50-0.99). Among adults presenting with ACS as a first manifestation of ASCVD, previous statin therapy is associated with a reduced risk of AHF and improved survival from AHF. (International Survey of Acute Coronary Syndromes [ISACS] Archives; NCT04008173).

Sections du résumé

BACKGROUND
There is uncertainty regarding the impact of statins on the risk of atherosclerotic cardiovascular disease (ASCVD) and its major complication, acute heart failure (AHF).
OBJECTIVES
The aim of this study was to investigate whether previous statin therapy translates into lower AHF events and improved survival from AHF among patients presenting with an acute coronary syndrome (ACS) as a first manifestation of ASCVD.
METHODS
Data were drawn from the International Survey of Acute Coronary Syndromes Archives. The study participants consisted of 14,542 Caucasian patients presenting with ACS without previous ASCVD events. Statin users before the index event were compared with nonusers by using inverse probability weighting models. Estimates were compared by test of interaction on the log scale. Main outcome measures were the incidence of AHF according to Killip class and the rate of 30-day all-cause mortality in patients presenting with AHF.
RESULTS
Previous statin therapy was associated with a significantly decreased rate of AHF on admission (4.3% absolute risk reduction; risk ratio [RR]: 0.72; 95% CI: 0.62-0.83) regardless of younger (40-75 years) or older age (interaction P = 0.27) and sex (interaction P = 0.22). Moreover, previous statin therapy predicted a lower risk of 30-day mortality in the subset of patients presenting with AHF on admission (5.2 % absolute risk reduction; RR: 0.71; 95% CI: 0.50-0.99).
CONCLUSIONS
Among adults presenting with ACS as a first manifestation of ASCVD, previous statin therapy is associated with a reduced risk of AHF and improved survival from AHF. (International Survey of Acute Coronary Syndromes [ISACS] Archives; NCT04008173).

Identifiants

pubmed: 35589164
pii: S0735-1097(22)04567-3
doi: 10.1016/j.jacc.2022.03.354
pii:
doi:

Substances chimiques

Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Banques de données

ClinicalTrials.gov
['NCT04008173']

Types de publication

Clinical Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2021-2033

Subventions

Organisme : British Heart Foundation
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures EMMACE was funded by the National Institute for Health Research and the British Heart Foundation. Dr Gale has received personal fees from AstraZeneca, Amgen, Bayer, and Daiichi-Sankyo outside the submitted work; and has received grants from Abbott and Bristol Myers Squibb outside the submitted work. Dr Badimon has served on the Scientific Advisory Board for Bayer; has served on the Scientific Advisory Board for and received personal fees and speaker fees from the International Aspirin Foundation during the conduct of the study; has served on the Scientific Advisory Board for Sanofi and Glycardial; has received personal fees from Lilly, AstraZeneca, BMS/Pfizer, and PACE; has received grants from AstraZeneca; has received personal fees and other from FICYE (Forum to Study Beer & Lifestyle), outside the submitted work; and has a patent APOj-Gly licensed, a patent IV_STATIN pending, and a patent DJ1-F pending. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Raffaele Bugiardini (R)

Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna, Bologna, Italy. Electronic address: raffaele.bugiardini@unibo.it.

Jinsung Yoon (J)

Google Cloud AI, Sunnyvale, California, USA; Department of Electrical and Computer Engineering, University of California, Los Angeles, Los Angeles, California, USA.

Guiomar Mendieta (G)

Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.

Sasko Kedev (S)

University Clinic of Cardiology, Faculty of Medicine Ss. Cyril and Methodius University, Skopje, Macedonia.

Marija Zdravkovic (M)

University Hospital Medical Center Bezanijska Kosa, Belgrade, Serbia.

Zorana Vasiljevic (Z)

Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Davor Miličić (D)

Department of Cardiovascular Diseases, University Hospital Center Zagreb, University of Zagreb, Zagreb, Croatia.

Olivia Manfrini (O)

Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna, Bologna, Italy.

Mihaela van der Schaar (M)

Department of Electrical and Computer Engineering, University of California, Los Angeles, Los Angeles, California, USA; Cambridge Centre for Artificial Intelligence in Medicine, Department of Applied Mathematics and Theoretical Physics and Department of Population Health, University of Cambridge, Cambridge, United Kingdom.

Chris P Gale (CP)

Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, United Kingdom.

Maria Bergami (M)

Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna, Bologna, Italy.

Lina Badimon (L)

Cardiovascular Research Program ICCC, IR-IIB Sant Pau, Hospital de la Santa Creu i Sant Pau, CiberCV-Institute Carlos III, Barcelona, Spain.

Edina Cenko (E)

Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna, Bologna, Italy.

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Classifications MeSH