Key result
Dapagliflozin plus semaglutide linked to ~56% lower heart failure risk vs. dapagliflozin alone.
Why the study?
Limited real-world data exist on the comparative impact of combining SGLT2 inhibitors and GLP-1 receptor agonists versus SGLT2 inhibitor monotherapy in patients with type 2 diabetes mellitus.
Does combination therapy with dapagliflozin and semaglutide improve cardiovascular and renal outcomes compared to dapagliflozin alone in adult patients with type 2 diabetes mellitus?
Cohort (n=539)
No
Does combination therapy with dapagliflozin and semaglutide improve cardiovascular and renal outcomes compared to dapagliflozin alone in adult patients with type 2 diabetes mellitus?
Relative Risk: 0.438 (95% CI 0.201–0.957)
p-value: p=0.038
In patients with T2DM, combining dapagliflozin with semaglutide may offer favorable renal outcomes and reduced heart failure risk compared to dapagliflozin alone, though prospective trials are needed.
May support adding semaglutide to dapagliflozin in T2DM for HF and renal benefits; leaves open prospective validation before practice change.
Introduction: Type 2 diabetes mellitus (T2DM) is a growing global health concern linked to increased cardiovascular and renal complications. Two emerging therapeutic classes, sodium-glucose cotransporter-2 inhibitors (SGLT2i) and glucagon like peptide-1 receptor agonists (GLP-1 RAs), have shown independent cardiometabolic benefits. However, limited realworld data exist on the comparative impact of combining these therapies versus using SGLT2i alone. Objective: To compare the cardiovascular and renal outcomes of dapagliflozin monotherapy versus combination therapy with once-weekly injectable semaglutide among patients with type 2 diabetes mellitus (T2DM). Methodology: In this retrospective cohort study, 539 adult patients with confirmed type 2 diabetes mellitus (T2DM; baseline HbA1c ≥6.5%) treated at King Abdulaziz Hospital, Al-Ahsa, were followed over six months. Patients received either dapagliflozin alone or in combination with semaglutide. Generalized Estimating Equations (GEE) were used to assess changes in glycemic control, cardiovascular events, lipid profile, and renal function, adjusting for time and sex. Results: = 0.13) did not reach statistical significance. No significant difference was observed in stroke risk. Most cardiovascular and renal markers improved modestly. Conclusion: Combination therapy was associated with favorable renal outcomes and a reduction in heart failure risk, despite inferior glycemic control and a non-significant trend toward reduced myocardial infarction risk. These findings suggest potential complementary effects of SGLT2i and GLP-1 RA treatment in high-risk patients. However, due to the retrospective, non-randomized design, causal relationships cannot be inferred, and residual confounding may exist. Prospective trials are warranted to confirm these associations and guide treatment optimization.
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Alharajin et al. (2026) conducted a cohort in Type 2 diabetes mellitus (n=539). Dapagliflozin combined with semaglutide vs. Dapagliflozin monotherapy was evaluated on Heart failure (RR 0.438, 95% CI 0.201-0.957, p=0.038). Combination therapy with dapagliflozin and semaglutide was associated with a significantly lower relative risk of heart failure (RR 0.438) and improved renal outcomes compared to dapagliflozin monotherapy.
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