Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
Dapagliflozin preserves kidney function and reduces albuminuria in children with chronic kidney disease.
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Assadi Farahnak, Bidabadi Elham, Mazaheri Mojgan, Ghane-Sharbaf Fatemeh, Faghihi Toktam, Naghshizadian Rama, Eskandarifar Alireza, Azarfar Anoush, Sadeghi-Bojd Simin, Abbasi Arash, Bazargani Behnaz, Safaei-Asl Afshin, Hooman Nakysa, Badeli Hamidreza
Аннотация
BACKGROUND: Sodium-glucose co-transporter 2 (SGLT2) inhibitors reduce CKD progression in adults; but pediatric evidence remains limited. We evaluated dapagliflozin in children with non-diabetic CKD.
METHODS: In this multicenter, randomized, open-label, endpoint-blinded controlled trial, 114 children with CKD stages 1-4 were assigned to dapagliflozin plus standard care (n=58) or standard care alone (n=56) for 4 months. Primary outcomes were changes in estimated glomerular filtration rate (eGFR) and urine albumin-to-creatinine ratio (UACR), analyzed using ANCOVA adjusted for baseline values.
RESULTS: Baseline characteristics were comparable between groups. At 4 months, eGFR increased in the dapagliflozin group (+2.1 mL/min/1.73 m²) and declined in controls (-4.2 mL/min/1.73 m²), yielding a between-group difference of 6.3 mL/min/1.73 m² (95% CI 2.1-10.5; p=0.004). UACR decreased significantly with dapagliflozin versus control (between-group difference -19.8 mg/g (95% CI: -21.9 to -18.6; p=0.002). Early CKD stages showed a shift toward lower albuminuria categories. No serious adverse events occurred.
CONCLUSION: Dapagliflozin was associated with short-term improvement in kidney function trajectory and reduction in albuminuria in children with CKD, with an acceptable safety profile.
METHODS: In this multicenter, randomized, open-label, endpoint-blinded controlled trial, 114 children with CKD stages 1-4 were assigned to dapagliflozin plus standard care (n=58) or standard care alone (n=56) for 4 months. Primary outcomes were changes in estimated glomerular filtration rate (eGFR) and urine albumin-to-creatinine ratio (UACR), analyzed using ANCOVA adjusted for baseline values.
RESULTS: Baseline characteristics were comparable between groups. At 4 months, eGFR increased in the dapagliflozin group (+2.1 mL/min/1.73 m²) and declined in controls (-4.2 mL/min/1.73 m²), yielding a between-group difference of 6.3 mL/min/1.73 m² (95% CI 2.1-10.5; p=0.004). UACR decreased significantly with dapagliflozin versus control (between-group difference -19.8 mg/g (95% CI: -21.9 to -18.6; p=0.002). Early CKD stages showed a shift toward lower albuminuria categories. No serious adverse events occurred.
CONCLUSION: Dapagliflozin was associated with short-term improvement in kidney function trajectory and reduction in albuminuria in children with CKD, with an acceptable safety profile.