Key result
SGLT2 inhibitors improve LA reservoir strain by ~4 percentage points post-ACS in diabetes.
Why the study?
The effect of SGLT2 inhibitors on left atrial deformation and heart failure biomarkers in patients with ACS and diabetes mellitus needed to be evaluated.
Does early initiation of SGLT2 inhibitors (empagliflozin or dapagliflozin) improve left atrial strain and NT-proBNP levels in patients with recent acute coronary syndrome and diabetes mellitus?
RCT (n=50)
Randomized 1:1
No
Does early initiation of SGLT2 inhibitors (empagliflozin or dapagliflozin) improve left atrial strain and NT-proBNP levels in patients with recent acute coronary syndrome and diabetes mellitus?
Early initiation of SGLT2 inhibitors in diabetic patients following acute coronary syndrome significantly improved left atrial strain, left ventricular function, and NT-proBNP levels at 3 months.
Supports early SGLT2i initiation post-ACS in diabetes; extends remodeling benefits beyond established HF populations.
Purpose To evaluate the effect of effect of Sodium–Glucose Co-Transporter 2 (SGLT2) Inhibitors on left atrial (LA) deformation and heart failure biomarkers in patients with Acute coronary syndrome (ACS) and diabetes mellitus (DM) Methods This prospective, case-control, single-center study enrolled 50 diabetic patients with recent ACS (<14 days). Participants were randomized into SGLT2i (empagliflozin/ dapagliflozin, n=25) and control (n=25) group. Echocardiographic parameters including LA strain by speckle-tracking echocardiography and NT-proBNP levels were assessed at baseline and 3 months. Results Baseline characteristics were comparable between groups. At 3-month follow-up, SGLT2i group demonstrated significant improvement in LA reservoir (29.08±7.23% to 33.36±6.45%, p<0.001), contractile strain (-17.16±5.27% to -19.88±5.41%, p=0.002), and conduit strain in 4-chamber view (-13.12±4.75% to -14.56±3.96%, p=0.007). Left ventricular systolic and diastolic functions also improved, with significant increases in LVEF (49.9% to 51.9%, p<0.001), reductions in E/e′ and LVESV, and enhanced GLS. NT-proBNP decreased markedly in the SGLT2i group (5541.6±8443.5 to 1179.6±1644.6 pg/ml, p=0.004). In the control group, only modest improvements in selected parameters were noted. Conclusions Early initiation of SGLT2 inhibitors in post-ACS diabetic patients significantly improved LA strain, LV remodelling and NT-proBNP, suggesting favourable cardiac reverse remodelling. These findings support the early incorporation of SGLT2i in secondary prevention strategies post-ACS, though larger trials with long-term outcomes are warranted.
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Khanna et al. (2026) conducted an RCT in Acute coronary syndrome and diabetes mellitus (n=50). SGLT2 inhibitors (empagliflozin or dapagliflozin) vs. Control was evaluated on Left atrial reservoir strain at 3 months (p=<0.001). SGLT2 inhibitors significantly improved LA reservoir strain (29.08% to 33.36%, p<0.001) and reduced NT-proBNP (p=0.004) at 3 months in diabetic patients post-ACS.
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