Effect of Tofogliflozin on Systolic and Diastolic Cardiac Function in Type 2 Diabetic Patients

Munemitsu Otagaki1, Koichiro Matsumura2, Hiromi Kin1

  • 1Department of Cardiology, Kansai Medical University Medical Center, 10-15, Fumizono-cho, Moriguchi, Osaka, 570-8507, Japan.

Abstract

Insights

Tofogliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor, improved cardiac function in type 2 diabetes mellitus (T2DM) patients. This SGLT2 inhibitor enhanced both systolic and diastolic left ventricular function, suggesting a potential cardiovascular benefit.

Area of Science:

  • Cardiology
  • Endocrinology
  • Pharmacology

Background:

  • Sodium glucose cotransporter 2 (SGLT2) inhibitors demonstrate cardiovascular benefits in diabetic patients.
  • The precise mechanisms underlying these cardiovascular improvements remain under investigation.
  • Type 2 diabetes mellitus (T2DM) is associated with increased cardiovascular risk and impaired cardiac function.

Purpose of the Study:

  • To evaluate the impact of tofogliflozin, an SGLT2 inhibitor, on cardiac function in patients with T2DM.
  • To assess changes in left ventricular systolic and diastolic function following tofogliflozin administration.

Main Methods:

  • A prospective study involving T2DM outpatients initiating tofogliflozin.
  • Echocardiography was performed before and at least 6 months after tofogliflozin initiation.
  • A propensity score-matched control group of T2DM patients on other glucose-lowering drugs was included for comparison.
  • Left ventricular ejection fraction (LVEF) assessed systolic function; early diastolic velocity (E/e') assessed diastolic function.

Main Results:

  • No significant baseline differences in patient characteristics or echocardiographic parameters between groups.
  • The tofogliflozin group showed a significant improvement in LVEF (5.0 ± 6.9%) compared to the control group (-0.6 ± 5.5%; p=0.006).
  • Diastolic function, measured by E/e', significantly improved in the tofogliflozin group (-1.7 ± 3.4) compared to the control group (0.7 ± 4.1; p=0.024).

Conclusions:

  • Tofogliflozin administration, in addition to conventional therapies, positively impacts left ventricular systolic function in T2DM patients.
  • Tofogliflozin also demonstrates a beneficial effect on left ventricular diastolic function in patients with T2DM.
  • These findings suggest SGLT2 inhibition may offer direct cardiac benefits beyond glycemic control in T2DM.

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