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Cardiometabolic outcomes with dapagliflozin after myocardial infarction by baseline ejection fraction: DAPA-MI

Lookup NU author(s): Dr David AustinORCiD

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This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND).


Abstract

© 2025 The Author(s). ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. Aims: In the randomized DAPA-MI clinical trial, 10 mg of dapagliflozin once daily improved cardiometabolic outcomes versus placebo after acute myocardial infarction (MI) in patients without established diabetes or heart failure (HF). We assessed associations between baseline left ventricular ejection fraction (LVEF) and cardiometabolic outcomes in DAPA-MI. Methods: The primary outcome, assessed using the win ratio method, was the hierarchical composite of death, hospitalization for HF, non-fatal MI, atrial fibrillation/flutter, Type 2 diabetes, New York Heart Association classification at last visit and body weight decrease of ≥5% from baseline to last visit. For the present analysis, patients were categorized using LVEF at randomization (<50% or ≥50%). Results: Of the DAPA-MI participants with available LVEF data who received ≥1 dose of study drug (n = 3751), 2913 (77.7%) had LVEF <50% and 838 (22.3%) had LVEF ≥50%. The primary hierarchical composite outcome resulted in a win ratio favouring dapagliflozin of 1.38 (95% CI: 1.21, 1.57; P < 0.001) in patients with LVEF <50% and 1.32 (1.00, 1.73; P = 0.048) in patients with LVEF ≥ 50% (P interaction = 0.76). In a sensitivity analysis excluding patients with LVEF <30%, the primary hierarchical composite outcome resulted in a win ratio favouring dapagliflozin of 1.40 (95% CI: 1.22, 1.61; P < 0.001). There were no significant interactions between baseline LVEF and any secondary outcomes. Conclusions: Regardless of baseline LVEF, dapagliflozin resulted in significant cardiometabolic benefits versus placebo, although there was no impact on the composite of cardiovascular death or hospitalization for HF.


Publication metadata

Author(s): Erlinge D, James S, Deanfield J, Eriksson N, de Belder M, Alchay M, Austin D, Jones DA, Ravn-Fischer A, Sederholm Lawesson S, Shah N, Strange JW, Szummer K, Ridderstrale W, Parvaresh Rizi E, Langkilde AM, Johansson PA, McGuire DK, Oldgren J, Storey RF

Publication type: Article

Publication status: Published

Journal: ESC Heart Failure

Year: 2025

Pages: Epub ahead of print

Online publication date: 16/09/2025

Acceptance date: 19/08/2025

Date deposited: 03/10/2025

ISSN (electronic): 2055-5822

Publisher: John Wiley and Sons Inc.

URL: https://doi.org/10.1002/ehf2.15420

DOI: 10.1002/ehf2.15420

Data Access Statement: Additional supporting information may be found online in the Supporting Information section at the end of the article.


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Funding

Funder referenceFunder name
AstraZeneca

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