Myocardial Infarction in Heart Failure With Preserved Ejection Fraction: Pooled Analysis of 3 Clinical Trials.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
08 2020
Historique:
received: 02 10 2019
revised: 06 01 2020
accepted: 11 02 2020
pubmed: 11 5 2020
medline: 13 5 2021
entrez: 11 5 2020
Statut: ppublish

Résumé

The authors investigated the relationship between past or incident myocardial infarction (MI) and cardiovascular (CV) events in heart failure with preserved ejection fraction (HFpEF). MI and HFpEF share some common risk factors. The prognostic significance of MI in patients with HFpEF is uncertain. The authors pooled data from 3 trials-CHARM Preserved (Candesartan Cilexietil in Heart Failure Assessment of Reduction in Mortality and Morbidity), I-Preserve (Irbesartan in Heart Failure With Preserved Systolic Function), and the Americas region of TOPCAT (Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist) (N = 8,916)-and examined whether MI before or following enrollment independently predicted CV death and heart failure (HF) hospitalization. At baseline, 2,668 patients (30%) had history of MI. Prior MI was independently associated with greater risk of CV death (4.7 vs. 3.5 events/100 patient-years [py], adjusted hazard ratio [HR]: 1.42 [95% confidence interval (CI): 1.23 to 1.64]; p < 0.001). Excess sudden death drove this difference (1.9 vs. 1.2 events/100 py, adjusted HR: 1.55 [95% CI: 1.23 to 1.97]; p < 0.001). There was no difference in HF hospitalization (5.9 vs. 5.5 events/100 py, adjusted HR: 1.05, 95% CI: 0.92 to 1.19) or HF death by prior MI. During follow-up, MI occurred in 336 patients (3.8%). Risk of CV death increased 31-fold in the first 30 days after first post-enrollment MI, and remained 58% higher beyond 1 year after MI. Risk of first or recurrent HF hospitalization increased 2.4-fold after MI. Prior MI in HFpEF is associated with greater CV and sudden death but similar risk of HF outcomes. Patients with HFpEF who experience MI are at high risk of subsequent CV death and HF hospitalization. These data highlight the importance of primary and secondary prevention of MI in patients with HFpEF. (Candesartan Cilexietil in Heart Failure Assessment of Reduction in Mortality and Morbidity [CHARM Preserved]; NCT00634712; Irbesartan in Heart Failure With Preserved Systolic Function [I-Preserve]; NCT00095238; and Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist [TOPCAT]; NCT00094302).

Sections du résumé

OBJECTIVES
The authors investigated the relationship between past or incident myocardial infarction (MI) and cardiovascular (CV) events in heart failure with preserved ejection fraction (HFpEF).
BACKGROUND
MI and HFpEF share some common risk factors. The prognostic significance of MI in patients with HFpEF is uncertain.
METHODS
The authors pooled data from 3 trials-CHARM Preserved (Candesartan Cilexietil in Heart Failure Assessment of Reduction in Mortality and Morbidity), I-Preserve (Irbesartan in Heart Failure With Preserved Systolic Function), and the Americas region of TOPCAT (Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist) (N = 8,916)-and examined whether MI before or following enrollment independently predicted CV death and heart failure (HF) hospitalization.
RESULTS
At baseline, 2,668 patients (30%) had history of MI. Prior MI was independently associated with greater risk of CV death (4.7 vs. 3.5 events/100 patient-years [py], adjusted hazard ratio [HR]: 1.42 [95% confidence interval (CI): 1.23 to 1.64]; p < 0.001). Excess sudden death drove this difference (1.9 vs. 1.2 events/100 py, adjusted HR: 1.55 [95% CI: 1.23 to 1.97]; p < 0.001). There was no difference in HF hospitalization (5.9 vs. 5.5 events/100 py, adjusted HR: 1.05, 95% CI: 0.92 to 1.19) or HF death by prior MI. During follow-up, MI occurred in 336 patients (3.8%). Risk of CV death increased 31-fold in the first 30 days after first post-enrollment MI, and remained 58% higher beyond 1 year after MI. Risk of first or recurrent HF hospitalization increased 2.4-fold after MI.
CONCLUSIONS
Prior MI in HFpEF is associated with greater CV and sudden death but similar risk of HF outcomes. Patients with HFpEF who experience MI are at high risk of subsequent CV death and HF hospitalization. These data highlight the importance of primary and secondary prevention of MI in patients with HFpEF. (Candesartan Cilexietil in Heart Failure Assessment of Reduction in Mortality and Morbidity [CHARM Preserved]; NCT00634712; Irbesartan in Heart Failure With Preserved Systolic Function [I-Preserve]; NCT00095238; and Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist [TOPCAT]; NCT00094302).

Identifiants

pubmed: 32387067
pii: S2213-1779(20)30142-6
doi: 10.1016/j.jchf.2020.02.007
pii:
doi:

Substances chimiques

Angiotensin II Type 1 Receptor Blockers 0
Benzimidazoles 0
Biphenyl Compounds 0
Diuretics 0
Tetrazoles 0
Spironolactone 27O7W4T232
Irbesartan J0E2756Z7N
candesartan S8Q36MD2XX

Banques de données

ClinicalTrials.gov
['NCT00094302']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

618-626

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL094301
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002541
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268200425207C
Pays : United States

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Jonathan W Cunningham (JW)

Brigham and Women's Hospital, Boston, Massachusetts.

Muthiah Vaduganathan (M)

Brigham and Women's Hospital, Boston, Massachusetts.

Brian L Claggett (BL)

Brigham and Women's Hospital, Boston, Massachusetts.

Jenine E John (JE)

Brigham and Women's Hospital, Boston, Massachusetts.

Akshay S Desai (AS)

Brigham and Women's Hospital, Boston, Massachusetts.

Eldrin F Lewis (EF)

Brigham and Women's Hospital, Boston, Massachusetts.

Michael R Zile (MR)

RHJ Department of Veterans Affairs Medical Center and Medical University of South Carolina, Charleston, South Carolina.

Peter Carson (P)

Veterans Affairs Medical Center, Washington DC.

Pardeep S Jhund (PS)

BHF Cardiovascular Research Centre, University of Glasgow, Glasgow, Scotland, United Kingdom.

Lars Kober (L)

Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.

Bertram Pitt (B)

University of Michigan School of Medicine, Ann Arbor, Michigan.

Sanjiv J Shah (SJ)

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Karl Swedberg (K)

University of Gothenburg, Gothenburg, Sweden.

Inder S Anand (IS)

VA Medical Center and University of Minnesota, Minneapolis, Minnesota.

Salim Yusuf (S)

Hamilton Health Sciences and McMaster University, Hamilton, Ontario, Canada.

John J V McMurray (JJV)

BHF Cardiovascular Research Centre, University of Glasgow, Glasgow, Scotland, United Kingdom.

Marc A Pfeffer (MA)

Brigham and Women's Hospital, Boston, Massachusetts.

Scott D Solomon (SD)

Brigham and Women's Hospital, Boston, Massachusetts. Electronic address: ssolomon@rics.bwh.harvard.edu.

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Classifications MeSH