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February 28, 2026Diabetes Research and Clinical Practice0 citations

SGLT2 inhibitors improve subclinical left ventricular systolic function independent of body mass index in patients with type 2 diabetes: A prospective strain imaging study

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ÖKÖmer KümetFPFuat PolatVCVeysi Can

Key Result

SGLT2 inhibitor therapy significantly improved global longitudinal strain at 6 months in patients with type 2 diabetes across both normal weight and overweight/obese categories (both p<0.001).

Key Points

  • This study aims to assess the impact of SGLT2 inhibitors on subclinical left ventricular function in relation to body mass index.
  • Enrolled 614 patients newly initiated on SGLT2 inhibitors stratified by BMI (normal weight and overweight/obesity).
  • Assessed global longitudinal strain using speckle tracking echocardiography at baseline and 6 months.
  • Significant GLS improvement in both groups (normal weight: -17.83% to -19.22%; overweight/obesity: -17.70% to -19.05%, both p < 0.001).
  • No significant difference in GLS improvement between BMI groups (p = 0.696).
  • Baseline GLS strongly predicted improvement (OR = 1.553, p < 0.001), while baseline BMI had no association.

Study Design

Type

Cohort (n=614)

Structured PICO

Does SGLT2 inhibitor therapy improve global longitudinal strain in patients with type 2 diabetes across different BMI categories?

P
Population
614 patients with type 2 diabetes newly initiated on SGLT2 inhibitors, stratified by BMI: normal weight (n=300) and overweight/obesity (n=314).
I
Intervention
SGLT2 inhibitors (newly initiated) for 6 months
O
Outcome
Global longitudinal strain (GLS) changes assessed by speckle tracking echocardiography at 6 monthssurrogate

SGLT2 inhibitors are associated with significant improvements in subclinical left ventricular systolic function (GLS) at 6 months in patients with type 2 diabetes, regardless of baseline BMI.

Main Result

p-value: p=<0.001

Limitations

  • Causality cannot be established without controls
  • BMI imperfectly measures adiposity
  • causality cannot be established without controls

Abstract

BACKGROUND Type 2 diabetes mellitus is associated with subclinical left ventricular dysfunction. SGLT2 inhibitors demonstrate cardiovascular benefits in trials, but their effects on subclinical myocardial function and relationship to body weight in clinical practice remain unclear. This study examined global longitudinal strain (GLS) changes during SGLT2 inhibitor therapy across body mass index (BMI) categories. METHODS This prospective observational cohort enrolled 614 patients newly initiated on SGLT2 inhibitors (September 2022-May 2025), stratified by BMI: normal weight (n = 300) and overweight/obesity (n = 314). Speckle tracking echocardiography assessed GLS at baseline and 6 months. RESULTS Both groups showed significant GLS improvement (normal weight: -17.83 ± 1.30% to -19.22 ± 1.20%; overweight/obesity: -17.70 ± 1.48% to -19.05 ± 1.24%; both p < 0.001), with similar magnitude (p = 0.696). Overweight/obesity patients experienced modest BMI reduction (-0.66 kg/m2, p < 0.001); normal weight remained stable. Baseline GLS strongly predicted improvement (OR = 1.553, p < 0.001), while baseline BMI showed no association (OR = 1.000, p = 0.993). CONCLUSION SGLT2 inhibitor therapy was associated with similar subclinical left ventricular systolic function improvement across BMI categories. While causality cannot be established without controls and BMI imperfectly measures adiposity, findings align with randomized trial cardiovascular benefits, suggesting benefits may extend across the body weight spectrum.

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Cite This Study

Kümet et al. (2026) conducted a cohort in Type 2 diabetes mellitus (n=614). SGLT2 inhibitors vs. Baseline (pre-treatment) and across BMI categories was evaluated on Global longitudinal strain (GLS) changes at 6 months (p=<0.001). SGLT2 inhibitor therapy significantly improved global longitudinal strain at 6 months in patients with type 2 diabetes across both normal weight and overweight/obese categories (both p<0.001).

synapsesocial.com/papers/6a025a5c9cddff7633412b9chttps://doi.org/10.1016/j.diabres.2026.113147
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