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Sodium-Glucose Co-Transporter 2 Inhibitors' Use in Muscular Dystrophy-Related Cardiomyopathy: Data from a
Maria Vittoria Matassini1, Francesca Coraducci1, Nastasia Mancini2
1Cardiology Division-Intensive Cardiac Care Unit, Cardiovascular Department, Azienda Ospedaliero Universitaria Delle Marche, 60126 Ancona, Italy.
Sodium-glucose co-transporter 2 inhibitors (SGLT2i) show promise for treating heart failure in muscular dystrophy patients. This study found SGLT2i therapy to be safe, improving ejection fraction and functional capacity.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Cardiac involvement is a primary cause of mortality in muscular dystrophies (MDs).
- Limited evidence exists for guideline-directed heart failure (HF) therapies in MD patients.
- This study investigates sodium-glucose co-transporter 2 inhibitors (SGLT2i) for HF in MD.
Purpose of the Study:
- To assess the effectiveness and tolerability of SGLT2i in patients with MD and heart failure.
- To evaluate changes in left ventricular ejection fraction (LVEF) and functional capacity.
- To examine the impact on guideline-directed HF therapy prescription.
Main Methods:
- Retrospective, single-center study of MD patients treated with SGLT2i (empagliflozin or dapagliflozin).
- Data collected at baseline and follow-up included clinical, laboratory, echocardiographic, and functional parameters.
- Analysis focused on longitudinal changes in LVEF, fatigue scores, and HF medication use.
Main Results:
- SGLT2i therapy was well-tolerated in 24 MD patients with a median follow-up of 418 days.
- LVEF significantly improved from 41% to 44% (p=0.005).
- Functional capacity improved (FSS decreased, p<0.001), and use of MRAs and beta-blockers increased.
Conclusions:
- SGLT2i therapy is safe and offers modest LVEF improvement and reduced fatigue in MD patients with HF.
- The findings support SGLT2i as a potential treatment for this high-risk population.
- Larger prospective studies are warranted to confirm these results.
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Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Cardiomyopathy IV: Restrictive Cardiomyopathy

