Prospective study shows dapagliflozin lowers annual eGFR decline in CKD patients, suggesting safety and efficacy.
Goal. To evaluate the efficacy and safety of dapagliflozin in patients with chronic kidney disease (CKD) of various stages in routine clinical practice. Materials and methods. A prospective study conducted at the Republican Clinical Hospital in Makhachkala from November 2023 to April 2025 included 32 patients with stage 2-4 CKD. Participants were randomly assigned to dapagliflozin (10 mg/day) and placebo groups. The main endpoint was the time before a decrease in eGFR ≥50%, the development of terminal renal failure, or death from a renal/cardiovascular cause. Results. In the dapagliflozin group, there was a tendency to a lower incidence of primary and secondary adverse outcomes. The average annual decrease in eGFR in the dapagliflozin group was 2.0 ml/min/1.73 m2 compared with 3.1 ml/min/1.73 m2 in the placebo group (p=0.01). The frequency of side effects was comparable between the groups. Conclusions. Dapagliflozin has demonstrated a beneficial effect on the rate of decrease in renal function and the frequency of cardiorenal complications in CKD, confirming the possibility of its safe use even in patients with a marked decrease in eGFR.
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Maksimova et al. (2025) studied this question.
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