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SGLT2 Inhibitors Are Associated with Left Ventricular Reverse Remodeling in Patients with Non-Compaction
Andraž Cerar1, Gregor Poglajen1,2, Gregor Zemljič1
1Advanced Heart Failure and Transplantation Centre, Department of Cardiology, University Medical Centre Ljubljana, Zaloška 7, 1000 Ljubljana, Slovenia.
Sodium glucose co-transporter 2 inhibitors (SGLT2is) show promise for treating left ventricular non-compaction cardiomyopathy (LVNC). These SGLT2 inhibitors improved cardiac function and reverse remodeling in LVNC patients.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Sodium glucose co-transporter 2 inhibitors (SGLT2is) are established treatments for heart failure.
- Limited data exist on SGLT2i efficacy in patients with left ventricular non-compaction cardiomyopathy (LVNC).
Purpose of the Study:
- To investigate the clinical effects of dapagliflozin and empagliflozin in patients diagnosed with LVNC.
- To assess changes in cardiac function and reverse remodeling following SGLT2i initiation.
Main Methods:
- Prospective enrollment of 30 consecutive LVNC patients diagnosed via cardiac magnetic resonance (CMR).
- Collection of clinical, biochemical, and echocardiographic data at baseline and 12-month follow-up.
- Definition of treatment response as a ≥5% improvement in left ventricular ejection fraction (LVEF) at 12 months.
Main Results:
- SGLT2i therapy led to significant improvements in LVEF (32.1% to 43.5%), LVOT VTI, E/e', and TAPSE.
- Mean NT-proBNP levels decreased significantly from 2025 to 582 pg/mL.
- Eighteen patients (60%) demonstrated a favorable response, characterized by smaller baseline LV end-diastolic diameter and lower NT-proBNP levels compared to non-responders.
Conclusions:
- SGLT2 inhibitor therapy is linked to significant reverse remodeling and functional enhancement in LVNC patients.
- The therapeutic benefits of SGLT2is may be more pronounced in individuals with less advanced LVNC disease.
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