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Empagliflozin versus dapagliflozin for kidney outcomes in stage 3 chronic kidney disease: a propensity score-matched multi-center cohort study

Bharati J, Bosch NA, Upadhyay A

BMC nephrology, 2026

27,344 participants

Abstract

Background: Sodium-glucose cotransporter 2 (SGLT2)-inhibitors are key in chronic kidney disease (CKD) management with empagliflozin and dapagliflozin being the two most commonly used. Comparative data between them in CKD is limited.

Methods: A propensity score-matched cohort study was conducted using data from a network of 103 North American organizations. Adults with Stage 3 CKD who initiated empagliflozin or dapagliflozin between January 1, 2021 and December 31, 2023, were compared. The primary outcome was the composite of Stage 5 CKD or end-stage kidney disease (ESKD). Follow-up continued until outcome or up to 3 years (censored on April 3, 2026).

Results: 53,887 and 27,344 patients with Stage 3 CKD were initiated on empagliflozin and dapagliflozin, respectively. Among matched patients with Stage 3 CKD (N = 26,911 per group) empagliflozin initiation was associated with lower risk of Stage 5 CKD or ESKD (7.7% vs. 9.0%; HR: 0.84; 95% CI: 0.79 to 0.89; log-rank P < 0.001) over ~ 970 days. All-cause mortality was similar between groups. Stage 5 CKD and ESKD rates were lower in the empagliflozin group.

Conclusion: In this multi-center retrospective cohort study, the risk for Stage 5 CKD or ESKD was lower for patients with Stage 3 CKD who initiated empagliflozin versus dapagliflozin over ~ 2.5 years. Prospective studies are needed to confirm our findings.

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 27,344 participants or records.

How the five levels of evidence work. The level is assigned automatically from the abstract and can be wrong, so check the paper.

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