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.

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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