Key result
Empagliflozin reduces carotid intima-media thickness vs placebo in post-STEMI patients with type 2 diabetes.
Why the study?
Patients with type 2 diabetes and recent STEMI have accelerated atherosclerosis and high recurrent cardiovascular risk; the effects of empagliflozin on carotid ultrasound parameters were unclear.
Does empagliflozin reduce carotid intima-media thickness in type 2 diabetes patients post-ST-elevation myocardial infarction?
RCT (n=80)
Double-blind
1:1 block randomization
No
Does empagliflozin reduce carotid intima-media thickness in type 2 diabetes patients post-ST-elevation myocardial infarction?
Absolute Event Rate: -0.13% vs -0.01%
p-value: p=0.004
Three months of empagliflozin therapy in patients with type 2 diabetes following a STEMI reduces carotid intima-media thickness, suggesting early favorable vascular remodeling effects.
Empagliflozin may slow early carotid atherosclerosis in T2DM post-STEMI; extends SGLT2i vascular effects to CIMT surrogate in this population.
Background: Patients with type 2 diabetes (T2D) and recent ST-elevation myocardial infarction (STEMI) face accelerated atherosclerosis and a high risk of recurrent cardiovascular events. Sodium-glucose cotransporter-2 inhibitors (SGLT2i), particularly empagliflozin, offer proven cardioprotection in T2D. This study investigated the 3-month effects of empagliflozin on carotid intima-media thickness (CIMT) and Doppler hemodynamic parameters (resistive index [RI] and pulsatility index [PI]) in T2D patients post-STEMI. Methods: In this randomized clinical trial, 80 patients with T2D and a recent STEMI from Ayatollah Mousavi Hospital, Zanjan, Iran (from July to December 2025), were randomized in a 1:1 ratio to empagliflozin 10 mg daily or an identical placebo, in addition to standard therapy. The primary endpoint was the change in CIMT at 3 months, assessed using B-mode ultrasound. Secondary endpoints included changes in RI and PI, measured via Doppler ultrasound. Results: Follow-up data were available for 78 patients (two deaths in the intervention arm, both unrelated to the study drug). In the primary intention-to-treat analysis (n=80), empagliflozin was associated with a significant reduction in left CIMT compared with controls (median change=-0.13 mm vs. -0.01; within-group P=0.002; between-group ΔCIMT P=0.004; ANCOVA-adjusted P<0.001) versus controls (-0.01 mm). A smaller though statistically significant difference was also observed for right CIMT (ΔCIMT, P=0.021; ANCOVA-adjusted P=0.006). These findings remained consistent in the per-protocol analysis. After Bonferroni correction, the reduction in left CIMT remained significant, whereas the effect on right CIMT became more modest. No significant changes were observed in RI or PI. Conclusion: IRCT20230727058945N1.
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Sani et al. (2026) conducted an RCT in Type 2 diabetes and recent ST-elevation myocardial infarction (STEMI) (n=80). Empagliflozin vs. Placebo was evaluated on Change in left carotid intima-media thickness (CIMT) at 3 months (p=0.004). Empagliflozin significantly reduced left carotid intima-media thickness compared to placebo (median change -0.13 mm vs -0.01 mm) over 3 months in patients with type 2 diabetes post-STEMI.
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