SGLT2-inhibition and myocardial infarction size in patients with type 2 diabetes mellitus- Insights from an acute cardiovascular care center
- PMID: 40753226
- PMCID: PMC12317468
- DOI: 10.1186/s12872-025-04981-5
SGLT2-inhibition and myocardial infarction size in patients with type 2 diabetes mellitus- Insights from an acute cardiovascular care center
Abstract
Aims: This study aimed to assess the association between myocardial infarction (MI) size and clinical outcome with ongoing Sodium-glucose-cotransporter-2 inhibitor (SGLT2-i) use.
Methods and results: In this retrospective single-center cohort study 681 patients with MI and diabetes mellitus type 2 (T2DM) treated with percutaneous coronary intervention (PCI) between November 2015 and December 2023 were included. 105 patients received ongoing SGLT2-i therapy and 576 were taking other glucose-lowering medication at the time of admission. The primary outcome was the size of MI. MI size was determined by the peak high-sensitive troponinT (hs-TnT x ULN [upper limit of normal]) normalized on the endangered myocardial area (EMA). No significant statistical differences were observed in hs-TnT values (hsTnT x ULN: 55 [13-174] vs. 68 [22-182]; p = 0.36) and EMA (41 [29-59] vs. 35 [24-59] %; p = 0.24) between patients with and without SGLT2-i therapy. After augmented inverse-probability weighted analyses, ongoing SGLT2-i therapy was not significantly associated with a reduced MI size (difference between means hsTnT x ULN/EMA [1/%]: - 0.24 [95% confidence interval, - 2.95 to 2.48]; p = 0.54). Secondary outcomes were in-hospital major adverse events and length of intensive care unit (ICU) treatment. SGLT2-i use was not associated with fewer in-hospital adverse events (3.81, vs. 4.17% [95% CI, - 2.95 to 2.48], p = 0.94) or with fewer days on ICU (1 [1-1] vs. 1 [1-2] days, p = 0.78).
Conclusion: In this retrospective cohort study of T2DM patients presenting with MI, prior prescription of SGLT2-i was not associated with reduced MI size or fewer adverse events during hospitalization for MI treated with PCI.
Trial registration number and date: DRKS00032432 (Registration Date: 07 August 2023).
Keywords: Acute myocardial infarction; Diabetes mellitus.; Infarct size; SGLT2-inhibitors.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: The protocol and amendments were approved by the local ethics committee, privacy and security offices, and institutional review board (Ethik-Kommission Albert-Ludwigs-Universität Freiburg, 21-1667). The need for consent to participate was waived by the institutional review board. The study was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. Consent for publication: Not applicable. Competing interests: IB: speakers fee from Novartis, FB: none, TH: Travel Grants from Boston Scientific and Novartis, NL: speakers fee from BMS and Daiichi Sankyo, PB: consultant and speakers fee from AstraZeneca and Boehringer Ingelheim, DW: Honorary from Abiomed, Astra Zeneca, Bayer, Böhringer Ingelheim, Medtronic, Novartis, CV: none, DeW: research support from European Research Council, Deutsche Forschungsgemeinschaft, Else Kröner-Fresenius Stiftung. Honoraria: Novo Nordisc, Bayer, Novartis, UCB, Böhringer Ingelheim, CBO: research support from Haemonetics, Deutsche Forschungsgemeinschaft, Deutsche Herzstiftung, Else Kröner-Fresenius Stiftung Faculty of Medicine - Freiburg University; honoraria: Bayer Vital GmbH, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Ferrer, Johnson & Johnson.
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