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No Differences in Kidney Function Decline Between People With Type 2 Diabetes Starting a Sodium-Glucose Cotransporter 2 Inhibitor or a Glucagon-like Peptide-1 Receptor Agonist: A Real-world Retrospective Comparative Observational Study.
Bodini, Sara; Pieralice, Silvia; D'Onofrio, Luca; Mignogna, Carmen; Coraggio, Lucia; Amendolara, Rocco; Risi, Renata; Salducci, Mauro; Buzzetti, Raffaella; Maddaloni, Ernesto.
Afiliación
  • Bodini S; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Pieralice S; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • D'Onofrio L; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Mignogna C; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Coraggio L; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Amendolara R; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Risi R; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Salducci M; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
  • Buzzetti R; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy. Electronic address: raffaella.buzzetti@uniroma1.it.
  • Maddaloni E; Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Clin Ther ; 2024 Jul 03.
Article en En | MEDLINE | ID: mdl-38964935
ABSTRACT

PURPOSE:

Diabetic nephropathy represents the leading cause of end-stage kidney disease in developed countries. Cardiovascular outcome trials have found that in participants who received a glucagon-like peptide-1 receptor agonist (GLP1RA) and a sodium-glucose cotransporter 2 inhibitor (SGLT2i), the risk of incidence and progression of diabetic nephropathy in type 2 diabetes mellitus was reduced. The aim of this study was to compare the decline in estimated glomerular filtration rate (eGFR) among people taking a GLP1RA with that among people taking an SGLT2i in a real-world setting.

METHODS:

Data for 478 patients with type 2 diabetes mellitus who initiated therapy with a GLP1RA (n = 254) or an SGLT2i (n = 224) between January 1, 2018 and December 31, 2021 were extracted. The primary outcome was any reduction ≥30% in eGFR after the start of therapy. Weight loss and drug discontinuation were also assessed.

FINDINGS:

Over a median follow-up of 24 months, an eGFR reduction ≥30% occurred in 34 of 254 patients (13.4%) starting a GLP1RA and in 26 of 223 patients (11.6%) starting an SGLT2i (hazard ratio = 0.89; 95% CI, 0.54-1.49; P = 0.67). Median eGFR change over the whole follow-up was similar between groups (SGLT2i median, -2 mL/min/1.73 m2; 25th, 75th percentile, -13, 8 mL/min/1.73 m2; GLP1RA median, 0 mL/min/1.73 m2; 25th, 75th percentile, -10, 7 mL/min/1.73 m2; P = 0.54). No worsening of kidney function was observed, even when considering the ratio eGFR mean. The value of eGFR at baseline indicated a statistically significant indirect correlation with the observed absolute value of eGFR change over the follow-up (ρ = -0.36; P < 0.001). The difference in eGFR changes over time observed by eGFR categories was statistically significant (P = 0.0001) in both treatment groups. No significant differences in weight loss and drug discontinuations were observed between groups. IMPLICATIONS Although acting on different molecular mechanisms, both GLP1RA and SGLT2i might have similar effects on eGFR decline in diabetes, as suggested by the results of the present study conducted in a real-world setting. (Clin Ther. 2024;46XXX-XXX) © 2024 Elsevier HS Journals, Inc.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Ther Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Ther Año: 2024 Tipo del documento: Article País de afiliación: Italia
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