Diabetes complications

Long‐term preservation of kidney function with SGLT ‐2 inhibitors versus comparator drugs in people with type 2 diabetes and chronic kidney disease

Diabetes Obes MetabPublished Retrospective cohort study

Main finding · eGFR declineResult — go to the resultMean difference 1.43 mL/min/1.73 m²

Authors' conclusion

In this large, real-world cohort, initiation of SGLT2i was associated with a significantly slower decline in kidney function and improved albuminuria compared with other diabetes drugs, including GLP-1RA. These findings support SGLT2i as the most effective T2D treatment to slow CKD progression.

Study context

Population
Patients aged 18–80 years with T2D and chronic kidney disease (CKD) who initiated an SGLT2 inhibitors (SGLT2i) or other glucose-lowering medications (GLM) between 2015 and 2020; mean age 63 years, BMI 32 kg/m², HbA1c 8.2%matched cohort
Participants
2,020 vs 2,020
Exposure
SGLT2i vs other glucose-lowering medications
  • SGLT2in = 2,020
  • Other GLMn = 2,020reference
Outcome
Change in eGFR over time
Methodological detailsmulticentre, propensity-score matched, real-world
  • Multicentre
  • Propensity-score matched
  • Real-world

Main finding

eGFR decline

Mean difference

1.43 mL/min/1.73 m²

P = 0.048

As reported in the abstract

Observational data: associations, not effects.

Secondary outcomes

OutcomeEstimateP value
Albuminuria category improvementSGLT2i vs Comparators · greater likelihood of improvement with SGLT2iHR 1.17P = 0.007
≥40% eGFR reductionSGLT2i vs ComparatorsHR 0.63P = 0.004
eGFR slope, SGLT2i vs GLP-1RA subgroup (n = 1266/group)Better eGFR slope with SGLT2imean difference 0.62 mL/min/1.73 m²/yearP = 0.046

Original publication

Long‐term preservation of kidney function with SGLT ‐2 inhibitors versus comparator drugs in people with type 2 diabetes and chronic kidney disease. Diabetes Obes Metab. Published 2 July 2025. doi:10.1111/dom.16569

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.