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Impact of Dapagliflozin on the Left Ventricular Diastolic Function in Diabetic Patients with Heart Failure
Fumitaka Soga1, Hidekazu Tanaka1, Kazuhiro Tatsumi1,2
1Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.
Abstract:
Objective Our aim was to investigate the impact of the sodium glucose cotransporter type 2 (SGLT2) inhibitor on the left ventricular (LV) diastolic function in type 2 diabetes mellitus (T2DM) patients with chronic heart failure (HF) complicating cardiovascular risk factors. Methods We analyzed data from our previous prospective multicenter study, in which we investigated the effect of dapagliflozin on the LV diastolic function of T2DM patients with stable HF at five institutions in Japan. Patients who had been taking at least 1 antidiabetic drug other than SGLT2 inhibitors started treatment with dapagliflozin. Echocardiography was performed at baseline and six months after the administration of dapagliflozin. Cardiovascular risk factors other than T2DM were age, gender, hypertension, dyslipidemia, history of cardiovascular events and overweight. Results The LV diastolic function, defined as the ratio of the mitral inflow E to the mitral e' annular velocities (E/e'), significantly decreased from 9.3 to 8.5 by six months after the administration of dapagliflozin (p=0.020) as previously reported. A multivariate logistic regression analysis showed that dyslipidemia was the only independent determinant of improvement in the E/e' after the administration of dapagliflozin among cardiovascular risk factors. Furthermore, the relative change in the E/e' from baseline to six months after the administration of dapagliflozin for HF patients with preserved ejection fraction (HFpEF) and dyslipidemia was significantly larger than that for HFpEF patients without dyslipidemia (-15.2% vs. 29.6%, p=0.014), but no such finding was observed in non-HFpEF patients. Conclusion SGLT2 inhibitors may exert a more beneficial effect on the LV diastolic function for T2DM patients with stable HF, especially those with complicating dyslipidemia, than existing treatments.
Insights
Sodium glucose cotransporter type 2 (SGLT2) inhibitors improved left ventricular diastolic function in type 2 diabetes mellitus patients with heart failure. Dyslipidemia was a key factor in this improvement, particularly in heart failure with preserved ejection fraction patients.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (T2DM) and chronic heart failure (HF) often coexist, increasing cardiovascular risk.
- Left ventricular (LV) diastolic dysfunction is a common complication in T2DM patients with HF.
Purpose of the Study:
- To investigate the impact of sodium glucose cotransporter type 2 (SGLT2) inhibitors on LV diastolic function in T2DM patients with HF.
- To identify cardiovascular risk factors influencing the response to SGLT2 inhibitors.
Main Methods:
- Prospective multicenter study analyzing data from T2DM patients with stable HF in Japan.
- Administration of dapagliflozin to patients already on other antidiabetic drugs.
- Echocardiography performed at baseline and six months post-administration to assess LV diastolic function (E/e' ratio).
Main Results:
- Dapagliflozin significantly decreased the E/e' ratio, indicating improved LV diastolic function (9.3 to 8.5, p=0.020).
- Dyslipidemia was identified as the sole independent determinant of E/e' improvement.
- HF patients with preserved ejection fraction (HFpEF) and dyslipidemia showed a significantly greater improvement in E/e' compared to those without dyslipidemia (-15.2% vs. 29.6%, p=0.014).
Conclusions:
- SGLT2 inhibitors demonstrate a beneficial effect on LV diastolic function in T2DM patients with stable HF.
- The positive impact is particularly pronounced in patients with co-existing dyslipidemia, especially within the HFpEF subgroup.
- SGLT2 inhibitors may offer advantages over existing treatments for this patient population.
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