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Effect of DAPAgliflozin on Myocardial Fibrosis and Ventricular Function in Patients with ST-Segment Elevation
Luis Ortega-Paz1, Claudio Laudani1,2, Alessandro Sionis3,4,5
1Division of Cardiology, College of Medicine, University of Florida, Jacksonville, FL 32206, USA.
Insights
This study investigated dapagliflozin
Area of Science:
- Cardiology
- Pharmacology
Background:
- Myocardial fibrosis impairs ventricular function and prognosis post-ST-segment elevation myocardial infarction (STEMI).
- Sodium-glucose cotransporter 2 inhibitors (SGLT2is) demonstrate cardioprotective effects by mitigating fibrosis and fibroblast activity.
- The impact of SGLT2is on myocardial fibrosis in STEMI patients undergoing primary percutaneous coronary intervention (PCI) remains unevaluated.
Purpose of the Study:
- To assess the efficacy of dapagliflozin in reducing myocardial fibrosis and improving ventricular function in STEMI patients post-primary PCI.
- To evaluate changes in myocardial extracellular volume and cardiac remodeling using cardiac magnetic resonance (CMR).
Main Methods:
- The DAPA-STEMI trial was a phase III, multicenter, randomized, double-blind, placebo-controlled study.
- 54 STEMI patients (LVEF ≤ 50%) were randomized to receive dapagliflozin 10 mg or placebo daily for six months.
- Primary endpoint: change in remote myocardium extracellular volume fraction via CMR; secondary endpoints: changes in fibrosis biomarkers.
Main Results:
- The study was prematurely halted due to slow recruitment, with only 54 patients enrolled.
- Limited statistical power to detect significant differences in the primary endpoint between dapagliflozin and placebo groups.
Conclusions:
- The DAPA-STEMI trial, despite early termination, offers preliminary insights into dapagliflozin's potential effects on myocardial fibrosis and ventricular remodeling in STEMI patients.
- Further research with larger cohorts is warranted to confirm these findings.
Abstract:
Background: Myocardial fibrosis leads to ventricular dysfunction and worsened prognosis, especially after ST-segment elevation myocardial infarction (STEMI). Sodium-glucose cotransporter 2 inhibitors (SGLT2is) offer cardiovascular benefits by reducing markers of myocardial fibrosis and fibroblast activity. However, the effects of SGLT2i on myocardial fibrosis deposition among STEMI patients undergoing primary percutaneous coronary intervention (PCI) have not yet been evaluated. Study and Design: The effect of DAPAgliflozin on myocardial fibrosis and ventricular function in patients with STEMI (DAPA-STEMI) trial is a phase III, multicenter, randomized, double-blind, placebo-controlled trial. The study aims to assess the effects of dapagliflozin on myocardial fibrosis and ventricular function, evaluated using cardiac magnetic resonance (CMR), in STEMI patients undergoing primary PCI. Eligible patients were 30 to 85 years old and exhibited a left ventricular ejection fraction ≤ 50%. A total of 120 patients with STEMI were expected to be randomized 1:1 to receive dapagliflozin 10 mg or placebo daily for six months. The primary endpoint is the change in the extracellular volume fraction of the remote myocardium from baseline to six months, as measured by CMR. The secondary endpoints include changes in the circulating C-terminal propeptide of type I procollagen, N-terminal propeptide of type III procollagen, and Galectin-3 from baseline to six months. The study was stopped prematurely due to slow recruitment, with 54 enrolled patients, limiting the statistical power to detect changes in the primary endpoint between groups. Conclusions: The DAPA-STEMI trial will provide insights into the impact of dapagliflozin on myocardial fibrosis and ventricular remodeling in patients with STEMI undergoing primary PCI. Clinical Trial Registration Unique Identifier: NCT06619600.
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