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Non-randomized preprint on dapagliflozin and epicardial adipose tissue in HFpEFDapagliflozin linked to fat loss in heart failure patients

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Key Takeaway
Consider that dapagliflozin may reduce epicardial adipose tissue in HFpEF, but confirmatory trials are needed.

This preprint describes a non-randomized clinical trial in 60 patients with left ventricular diastolic dysfunction. The study investigated the addition of 10 mg of dapagliflozin once daily to standard medical therapy, compared to standard care alone. The primary outcome was a change in epicardial adipose tissue (EAT) volume.

The authors report that at baseline, EAT volume was significantly higher in the group receiving dapagliflozin plus standard care versus the standard care only group (p < 0.001). At follow-up, EAT volumes were comparable between the two groups (p = 0.081). Within the standard care group, the change in EAT volume was insignificant (p = 0.124), while within the dapagliflozin group, there was a significant reduction (p < 0.001). An interaction analysis confirmed a significant EAT reduction in the dapagliflozin group (p < 0.001).

The authors acknowledge key limitations, including the non-randomized design and the need for confirmation in randomized, outcome-driven trials. Safety data, including adverse events and discontinuations, were not reported. The findings are presented as an association, and the certainty is limited as this is a preprint.

Clinically, the results suggest a possible structural association between SGLT2 inhibitor use and reduced epicardial adipose tissue in this patient population. However, the evidence is preliminary, and practice changes should not be based on this single, non-randomized report.

A preprint study looked at how adding dapagliflozin affects heart tissue in people with heart failure. The research involved 60 patients who had left ventricular diastolic dysfunction. These patients were already receiving standard medical therapy. Some received an extra 10 mg of dapagliflozin once daily, while others continued with standard care only. The main goal was to see changes in epicardial adipose tissue volume, which is fat surrounding the heart.

At the start of the study, the group taking dapagliflozin had significantly higher levels of this heart fat compared to the standard care group. Over the follow-up period, the group taking the medication saw a significant reduction in fat volume. The standard care group showed no significant change. The difference between the two groups at the end of the study was not statistically significant, but the medication group did show a clear drop in fat.

No safety issues were reported in this small study. However, the researchers note that the study was not randomized. This means the results are considered an association rather than proof of cause and effect. The findings warrant confirmation in larger, randomized trials before they change medical practice.

What this means for you:
This preprint study links dapagliflozin to reduced heart fat in a small group of patients.

Study Details

Sample sizen = 60
EvidenceLevel 5
PublishedApr 2026
View Original Abstract ↓
BACKGROUND: Heart failure with preserved ejection fraction is the fastest-growing subtype of heart failure, especially among the elderly. AIM: It is aimed to determine whether the addition of 10 mg of Dapagliflozin for HFpEF patient can lead to a decrease in epicardial adipose tissue volume. METHODS: this non-randomized clinical trial included 60 patients presented with left ventricular diastolic dysfunction (30 patients fulfilling HFpEF diagnostic criteria received dapagliflozin 10 mg once daily in addition to standard medical therapy and 30 patients with LV diastolic dysfunction who did not meet HFpEF criteria received standard medical care only). RESULTS: The mean EAT volume was significantly (p < 0.001) higher in the HFpEF + dapagliflozin group vs. standard care group at baseline while it was comparable in the two groups at follow-up (p = 0.081). For within group comparisons, insignificant (p = 0.124) change was recorded for the standard care group while there was significant reduction in the HFpEF + dapagliflozin arm (p < 0.001). Additionally, EAT reduction in the HFpEF + dapagliflozin group was confirmed by the interaction between time and treatment modality (p < 0.001). CONCLUSIONS: SGLT2 inhibitor use was associated with a significant reduction in epicardial adipose tissue, a fat depot implicated in HFpEF pathophysiology. This finding suggested a possible structural association that warrants confirmation in randomized out-come driven trials. TRIAL REGISTRATION: NO. (NCT06510270) (first submitted date 15/7/2024, first posted date 19/7/2024).
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