Type 2 & other diabetes

Effects of empagliflozin on conventional and exploratory acute and chronic kidney outcomes: an individual participant-level meta-analysis

Lancet Diabetes EndocrinolPublished Individual participant-level meta-analysis of randomised placebo-controlled trials

Authors' conclusion

SGLT2 inhibition reduces risk of acute and chronic kidney outcomes irrespective of the size of the acute dip in eGFR. Kidney benefits are evident irrespective of diabetes status, heart failure status, primary cause of kidney disease, and markers of severity of these diseases.

Study context

Population
Participants in EMPA-REG OUTCOME, EMPEROR-Reduced, EMPEROR-Preserved and EMPA-KIDNEY
Participants
23,340 participants4 RCTs
Comparison
Empagliflozin vs placebo
Outcome
Conventional and exploratory acute and chronic kidney outcomes
Methodological detailstests for heterogeneity and trend
  • Tests for heterogeneity and trend

Pooled result

As reported in the abstract

Empagliflozin vs PlaceboHazard ratio (95% CI)
Marker of AKI (≥50% increase in serum creatinine in consecutive samples); 1573 outcomes; 20% reduction
0.80(0.72–0.88)
AKI adverse events; 694 outcomes; 27% reduction
0.73(0.63–0.85)
Categorical CKD progression; 1403 outcomes; 30% reduction
0.70(0.63–0.78)
Kidney failure; 490 outcomes; 34% reduction
0.66(0.55–0.79)
Slowing of chronic annual rate of estimated glomerular filtration rate (eGFR) decline
64% (95% CI 59-69)
Slowing of off-treatment dip-free slope, post-hoc, subset of 10 630 participants (54-73)
64%

Further pooled results

Kidney benefits similar in subgroups by predicted size of acute eGFR dip, and present irrespective of diabetes or HF status, kidney function, or albuminuria

Safety

OutcomeHR (CI)
AKI adverse events694 outcomes; 27% reduction0.73 (0.63–0.85)

Original publication

Effects of empagliflozin on conventional and exploratory acute and chronic kidney outcomes: an individual participant-level meta-analysis. Lancet Diabetes Endocrinol. Published 11 October 2025. doi:10.1016/s2213-8587(25)00222-0

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