Related Experiment Video
Updated: Jul 12, 2025

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Dapagliflozin Improved Cardiac Function and Structure in Diabetic Patients with Preserved Ejection Fraction: Results
Marcelino Cortés1, Oscar Lorenzo2,3, Jairo Lumpuy-Castillo2,3
1Cardiology Department, Fundación Jiménez Díaz Hospital, 28040 Madrid, Spain.
Insights
Sodium-glucose cotransporter inhibitors (SGLT2i) improve cardiac structure and function in diabetic patients. Dapagliflozin reduced left ventricle mass and improved cardiac strain and relaxation, benefiting heart health.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Sodium-glucose cotransporter inhibitors (SGLT2i) show cardiovascular benefits in diabetes and heart failure (HF).
- Mechanisms for SGLT2i cardiovascular benefits are unclear, with conflicting data.
- SGLT2i effects on cardiac structure and function in patients with preserved ejection fraction require further investigation.
Purpose of the Study:
- To analyze the effect of dapagliflozin on cardiac structure and function.
- To assess changes in diabetic patients with normal ejection fraction.
- To investigate potential mechanisms behind SGLT2i cardiovascular benefits.
Main Methods:
- Prospective study including 31 diabetic patients without prior SGLT2i use.
- Dapagliflozin treatment initiated, followed for 6 months.
- Echocardiography (standard, 3D, speckle tracking), ECG, and laboratory analyses performed at baseline and follow-up.
Main Results:
- A significant reduction in 3D-estimated left ventricle mass (18 g, p=0.028).
- Improved left ventricle global longitudinal strain (LV-GLS) (0.3, p=0.036) and increased isovolumetric relaxation time (IVRT) (10.5 ms, p=0.05).
- Decreased plasma levels of creatin-kinase (CK-MB) and atrial natriuretic peptide (ANP).
Conclusions:
- Dapagliflozin treatment is associated with structural cardiac improvements (reduced myocardial mass).
- Functional cardiac improvements include enhanced LV-GLS and IVRT in diabetic patients with normal ejection fraction.
- SGLT2 inhibition demonstrates beneficial effects on cardiac remodeling and function in this population.
Abstract:
Sodium-glucose cotransporter inhibitors (SGLT2i) have demonstrated a reduction in cardiovascular events in diabetes and heart failure (HF). The mechanisms underlying this benefit are not well known and data are contradictory. The purpose of this study is to analyse the effect of dapagliflozin on cardiac structure and function in patients with normal ejection fraction. Between October 2020 and October 2021, we consecutively included 31 diabetic patients without prior history of SGLT2i use. In all of them, dapagliflozin treatment was started. At inclusion and during six months of follow-up, different clinical, ECG, analytical, and echocardiographic (standard, 3D, and speckle tracking) variables were recorded. After a follow-up period of 6.6 months, an average reduction of 18 g (p = 0.028) in 3D-estimated left ventricle mass was observed. An increase in absolute left ventricle global longitudinal strain (LV-GLS) of 0.3 (p = 0.036) was observed, as well as an increase in isovolumetric relaxation time (IVRT) of 10.5 ms (p = 0.05). Moreover, dapagliflozin decreased the levels of plasma creatin-kinase (CK-MB) and atrial natriuretic peptide (ANP). In conclusion, our data show that the use of SGLT2i is associated with both structural (myocardial mass) and functional (IVRT, LV-GLS) cardiac improvements in a population of diabetic patients with normal ejection fraction.
More Related Videos
05:58Mouse Electroacupuncture Fixation Device Fabrication for Electroacupuncture Pretreatment in Diabetic Cardiomyopathy Mouse Model
Published on: April 18, 2025
07:24Reduction in Left Ventricular Wall Stress and Improvement in Function in Failing Hearts using Algisyl-LVR
Published on: April 8, 2013
Related Concept Videos
Dipeptidyl Peptidase 4 Inhibitors
Heart Failure V: Medical Management
Heart Failure Drugs: Diuretics
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
Oral Hypoglycemic Agents: Biguanides and Glitazones