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Updated: Oct 5, 2025

Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
SGLT2 inhibitors in non-diabetic kidney disease
1Department of Nephrology, Charles University in Prague, Czech Republic.
Abstract:
There is an accumulating evidence demonstrating renoprotective and cardioprotective role of sodium-glucose cotransporter 2 (SGLT2) inhibitors in early to advanced diabetic kidney disease. Data from recently published Dapagliflozin and Prevention of Adverse Outcomes in the Chronic Kidney Disease (DAPA-CKD) trial clearly show that dapagliflozin is similarly renoprotective in non-diabetic chronic kidney disease in a wide range of estimated glomerular filtration rate (eGFR) of 25-75 mL/min/1.73 m2 (0.42-1.25 mL/s/1.73 m2) and albumin/creatinine ratio 200-5000 mg/g (approx. 20-500 mg/mmol). Patients with type 1 diabetes, autosomal dominant polycystic kidney disease, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis and lupus nephritis were excluded from the study, but, on the other hand, prespecified subanalysis demonstrated that dapagliflozin should be renoprotective also in patients with immunoglobulin A (IgA) nephropathy. The renoprotective effect of SGLT2 inhibitors is additive to the renoprotection conferred with blockers of renin-angiotensin system, including both inhibitors of angiotensin converting enzyme (ACEI), or angiotensin receptor blocker (ARB). These promising data will be hopefully confirmed by the ongoing the Study of Heart and Kidney Protection With Empagliflozin (EMPA-KIDNEY) trial, the results of which are expected later in 2022.
Insights
Sodium-glucose cotransporter 2 (SGLT2) inhibitors, like dapagliflozin, show renoprotective effects in chronic kidney disease, even without diabetes. Their benefits are enhanced when combined with renin-angiotensin system blockers.
Area of Science:
- Nephrology
- Pharmacology
- Cardiology
Background:
- Accumulating evidence supports the renoprotective and cardioprotective roles of sodium-glucose cotransporter 2 (SGLT2) inhibitors in diabetic kidney disease.
- The Dapagliflozin and Prevention of Adverse Outcomes in the Chronic Kidney Disease (DAPA-CKD) trial demonstrated dapagliflozin's renoprotective efficacy in non-diabetic chronic kidney disease across a broad range of estimated glomerular filtration rates (eGFR) and albumin/creatinine ratios.
Discussion:
- Dapagliflozin exhibited renoprotective effects in non-diabetic chronic kidney disease patients, irrespective of diabetes status.
- While specific conditions like type 1 diabetes, autosomal dominant polycystic kidney disease, ANCA-associated vasculitis, and lupus nephritis were excluded, subanalyses suggested potential benefits in IgA nephropathy.
- The renoprotective impact of SGLT2 inhibitors is additive to that of renin-angiotensin system blockers, including ACE inhibitors (ACEI) and angiotensin receptor blockers (ARB).
Key Insights:
- SGLT2 inhibitors offer renoprotection in chronic kidney disease (CKD) beyond diabetic nephropathy.
- Dapagliflozin demonstrated efficacy in non-diabetic CKD patients with varying eGFR and albuminuria levels.
- Combined therapy with SGLT2 inhibitors and RAS blockers provides additive renoprotection.
Outlook:
- Further confirmation is anticipated from the ongoing Study of Heart and Kidney Protection With Empagliflozin (EMPA-KIDNEY) trial.
- These findings may expand the therapeutic applications of SGLT2 inhibitors in kidney disease management.
- Continued research will elucidate the full potential of SGLT2 inhibitors in diverse CKD populations.
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