Secondary analysis of the EMPACT-MI trial reveals cardiovascular–kidney efficacy and safety of empagliflozin after acute myocardial infarction

Data on the cardiovascular-kidney effects and safety of empagliflozin among patients with acute myocardial infarction are limited. EMPACT-MI (Study to Evaluate the Effect of Empagliflozin on Hospitalization for Heart Failure and Mortality in Patients with Acute Myocardial Infarction) was a double-blind, multicenter clinical trial that randomized 6,522 patients with acute myocardial infarction and risk for heart failure to empagliflozin or placebo. Here we show in this secondary analysis that the mean estimated glomerular filtration rate at baseline was 76.1 ml min<sup>-1</sup> 1.73 m<sup>-</sup><sup>2</sup> (s.d. = 19.9 ml min<sup>-1</sup> 1.73 m<sup>-</sup><sup>2</sup>), with longitudinal kidney function data available for 1,152 (17.7%) treated patients from select countries. By 24 months, compared with baseline, the estimated glomerular filtration rate was similar in the empagliflozin group but declined in the placebo group (P = 0.01). Empagliflozin reduced the total adverse events of heart failure or all-cause mortality irrespective of kidney function (P<sub>interaction</sub> = 0.30). Thirty-day adverse event rates were similar by treatment group and consistent across baseline kidney function. Empagliflozin had kidney-protective effects, reduced heart failure outcomes and was safe to initiate soon after acute myocardial infarction across baseline kidney function.

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Journal
Nature Cardiovascular Research
Published
2025-06-13
DOI
https://doi.org/10.1038/s44161-025-00657-7
Citations
2
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
2.59

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article

Secondary analysis of the EMPACT-MI trial reveals cardiovascular–kidney efficacy and safety of empagliflozin after acute myocardial infarction

Stefan D. Anker, W. Schuyler Jones, Josephine Harrington, Mark C. Petrie et al.
2 citations
Nature Cardiovascular Research
Diabetes Treatment and Management
2.59
article

Secondary analysis of the EMPACT-MI trial reveals cardiovascular–kidney efficacy and safety of empagliflozin after acute myocardial infarction

Stefan D. Anker, W. Schuyler Jones, Josephine Harrington, Mark C. Petrie, Deepak L. Bhatt, Mikhail Sumin, Rahul Aggarwal, Adrian F. Hernandez, Javed Butler, Dominik Steubl, Michaela Mattheus, Jacob A. Udell, Vikram Thanam
article en
2 citations

Abstract

Data on the cardiovascular-kidney effects and safety of empagliflozin among patients with acute myocardial infarction are limited. EMPACT-MI (Study to Evaluate the Effect of Empagliflozin on Hospitalization for Heart Failure and Mortality in Patients with Acute Myocardial Infarction) was a double-blind, multicenter clinical trial that randomized 6,522 patients with acute myocardial infarction and risk for heart failure to empagliflozin or placebo. Here we show in this secondary analysis that the mean estimated glomerular filtration rate at baseline was 76.1 ml min<sup>-1</sup> 1.73 m<sup>-</sup><sup>2</sup> (s.d. = 19.9 ml min<sup>-1</sup> 1.73 m<sup>-</sup><sup>2</sup>), with longitudinal kidney function data available for 1,152 (17.7%) treated patients from select countries. By 24 months, compared with baseline, the estimated glomerular filtration rate was similar in the empagliflozin group but declined in the placebo group (P = 0.01). Empagliflozin reduced the total adverse events of heart failure or all-cause mortality irrespective of kidney function (P<sub>interaction</sub> = 0.30). Thirty-day adverse event rates were similar by treatment group and consistent across baseline kidney function. Empagliflozin had kidney-protective effects, reduced heart failure outcomes and was safe to initiate soon after acute myocardial infarction across baseline kidney function.

Nature Cardiovascular ResearchVol. 4(6)
Brigham and Women's Hospital (US), Boehringer Ingelheim (Germany) (DE), Harvard University (US), Duke University (US), University of Toronto (CA), Women's College Hospital (CA), Toronto General Hospital (CA), TUM Klinikum (DE), British Heart Foundation (GB), University of Mississippi (US), Clinical Research Institute (US), Mount Sinai Hospital (US), Mount Sinai Hospital (US), Baylor Medical Center at Garland (US), German Centre for Cardiovascular Research (DE), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), University of Glasgow (GB), Icahn School of Medicine at Mount Sinai (US)
Boehringer Ingelheim, Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, Boehringer Ingelheim, Boston Scientific Corporation, Regeneron Pharmaceuticals, LivaNova, Novavax, Cytokinetics, Impulse Dynamics, Moderna, Horizon Therapeutics, Novo Nordisk, Astellas Pharma, Servier, National Institutes of Health, American Regent, National Heart, Lung, and Blood Institute
Openalex Percentile: Top 10%
Diabetes Treatment and Management
2.59
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