Glomerular and tubular effects of dapagliflozin, eplerenone and their combination in patients with chronic kidney disease: A post‐hoc analysis of the ROTATE‐3 study

Author:

Lieverse Tom T. G. F.1ORCID,Puchades Maria J.2,Mulder Udo D. J.3,Provenzano Michele45,Krenning Guido1,Jongs Niels1,Wink Simon E.1,Slart Riemer H. J. A.6,Andreucci Michele7,D'Marco Luis8ORCID,De Nicola Luca9,Gorriz Jose L.2,Heerspink Hiddo J. L.1ORCID

Affiliation:

1. Department of Clinical Pharmacy and Pharmacology University of Groningen, University Medical Center Groningen Groningen The Netherlands

2. Department of Nephrology University Clinical Hospital Valencia, INCLIVA, University of Valencia Valencia Spain

3. Department of Internal Medicine, Division of Vascular Medicine University of Groningen, University Medical Center Groningen Groningen The Netherlands

4. Nephrology, Dialysis and Renal Transplant Unit IRCCS Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy

5. Department of Medical and Surgical Sciences (DIMEC) Alma Mater Studiorum University of Bologna Bologna Italy

6. Department of Nuclear Medicine and Molecular Imaging University of Groningen, University Medical Center Groningen Groningen The Netherlands

7. Department of Health Sciences 'Magna Graecia' University of Catanzaro Catanzaro Italy

8. Universidad Cardenal Herrera‐CEU, CEU Universities Valencia Spain

9. Department of Advanced Medical and Surgical Sciences University L. Vanvitelli Naples Italy

Abstract

AbstractAimSodium‐glucose co‐transporter 2 inhibitors and mineralocorticoid receptor antagonists reduce albuminuria and the risk of kidney failure. The aim of this study was to investigate the effects of both agents alone and in combination on markers of the glomerular endothelial glycocalyx and tubular function.MethodsThis post‐hoc analysis utilized data of the ROTATE‐3 study, a randomized cross‐over study in 46 adults with chronic kidney disease and urinary albumin excretion ≥100 mg/24 h, who were treated for 4 weeks with dapagliflozin, eplerenone or its combination. The effects of dapagliflozin, eplerenone and the combination on outcome measures such as heparan sulphate, neuro‐hormonal markers and tubular sodium handling were assessed with mixed repeated measures models.ResultsThe mean percentage change from baseline in heparan sulphate after 4 weeks treatment with dapagliflozin, eplerenone or dapagliflozin‐eplerenone was −34.8% (95% CI −52.2, −10.9), −5.9% (95% CI −32.5, 31.3) and −28.1% (95% CI −48.4, 0.1) respectively. The mean percentage change from baseline in plasma aldosterone was larger with eplerenone [38.9% (95% CI 2.8, 87.7)] and dapagliflozin‐eplerenone [32.2% (95% CI −1.5, 77.4)], compared with dapagliflozin [−12.5% (95% CI −35.0, 17.8)], respectively. Mean percentage change from baseline in copeptin with dapagliflozin, eplerenone or dapagliflozin‐eplerenone was 28.4% (95% CI 10.7, 49.0), 4.2% (95% CI −10.6, 21.4) and 23.8% (95% CI 6.6, 43.9) respectively. Dapagliflozin decreased proximal absolute sodium reabsorption rate by 455.9 mmol/min (95% CI −879.2, −32.6), while eplerenone decreased distal absolute sodium reabsorption rate by 523.1 mmol/min (95% CI −926.1, −120.0). Dapagliflozin‐eplerenone decreased proximal absolute sodium reabsorption [−971.0 mmol/min (95% CI −1411.0, −531.0)], but did not affect distal absolute sodium reabsorption [−9.2 mmol/min (95% CI −402.0, 383.6)].ConclusionsDapagliflozin and eplerenone exert different effects on markers of glomerular and tubular function supporting the hypothesis that different mechanistic pathways may account for their kidney protective effects.

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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