<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(11)</volume><submitter>Angermann CE</submitter><pubmed_abstract>Sodium-glucose co-transporter-2 (SGLT2) inhibitors improve clinical outcomes in patients with heart failure (HF), but mechanisms of action are incompletely understood. In the EMPA-TROPISM trial, empagliflozin reversed cardiac remodeling and increased physical capacity in stable non-diabetic patients with systolic HF. Here we explore, post hoc, whether treatment effects in this cohort, comprising patients who had a high prevalence of iron deficiency, were related to iron metabolism. Myocardial iron content estimated by cardiac magnetic resonance T2* quantification increased after initiation of empagliflozin but not placebo (treatment effect: P = 0.01). T2* changes significantly correlated with changes in left ventricular volumes, mass and ejection fraction, peak oxygen consumption and 6-min</pubmed_abstract><journal>Nature cardiovascular research</journal><pagination>1032-1043</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11358002</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Empagliflozin effects on iron metabolism as a possible mechanism for improved clinical outcomes in non-diabetic patients with systolic heart failure.</pubmed_title><pmcid>PMC11358002</pmcid><pubmed_authors>Zeller T</pubmed_authors><pubmed_authors>Frantz S</pubmed_authors><pubmed_authors>Requena-Ibanez JA</pubmed_authors><pubmed_authors>Maack C</pubmed_authors><pubmed_authors>Sehner S</pubmed_authors><pubmed_authors>Santos-Gallego CG</pubmed_authors><pubmed_authors>Gerhardt LMS</pubmed_authors><pubmed_authors>Ertl G</pubmed_authors><pubmed_authors>Badimon JJ</pubmed_authors><pubmed_authors>Angermann CE</pubmed_authors><pubmed_authors>Sanz J</pubmed_authors><pubmed_authors>Fuster V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Empagliflozin effects on iron metabolism as a possible mechanism for improved clinical outcomes in non-diabetic patients with systolic heart failure.</name><description>Sodium-glucose co-transporter-2 (SGLT2) inhibitors improve clinical outcomes in patients with heart failure (HF), but mechanisms of action are incompletely understood. In the EMPA-TROPISM trial, empagliflozin reversed cardiac remodeling and increased physical capacity in stable non-diabetic patients with systolic HF. Here we explore, post hoc, whether treatment effects in this cohort, comprising patients who had a high prevalence of iron deficiency, were related to iron metabolism. Myocardial iron content estimated by cardiac magnetic resonance T2* quantification increased after initiation of empagliflozin but not placebo (treatment effect: P = 0.01). T2* changes significantly correlated with changes in left ventricular volumes, mass and ejection fraction, peak oxygen consumption and 6-min</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2026-06-02T09:13:02.817Z</modification><creation>2025-04-05T18:38:24.563Z</creation></dates><accession>S-EPMC11358002</accession><cross_references><pubmed>39196095</pubmed><doi>10.1038/s44161-023-00352-5</doi></cross_references></HashMap>