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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
被引:0
|作者:
Lieverse, Tom T. G. F.
[1
]
Puchades, Maria J.
[2
]
Mulder, Udo D. J.
[3
]
Provenzano, Michele
[4
,5
]
Krenning, Guido
[1
]
Jongs, Niels
[1
]
Wink, Simon E.
[1
]
Slart, Riemer H. J. A.
[6
]
Andreucci, Michele
[7
]
D'Marco, Luis
[8
]
De Nicola, Luca
[9
]
Gorriz, Jose L.
Heerspink, Hiddo J. L.
[1
,10
]
机构:
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
[2] Univ Valencia, Univ Clin Hosp Valencia, Dept Nephrol, INCLIVA, Valencia, Spain
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Vasc Med, Groningen, Netherlands
[4] IRCCS Azienda Osped Univ Bologna, Nephrol Dialysis & Renal Transplant Unit, Bologna, Italy
[5] Univ Bologna, Dept Med & Surg Sci DIMEC, Alma Mater Studiorum, Bologna, Italy
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Nucl Med & Mol Imaging, Groningen, Netherlands
[7] Magna Graecia Univ Catanzaro, Dept Hlth Sci, Catanzaro, Italy
[8] CEU Univ, Univ Cardenal Herrera CEU, Valencia, Spain
[9] Univ Campania L Vanvitelli, Dept Adv Med & Surg Sci, Naples, Italy
[10] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Hanzepl 1, NL-9700 RB Groningen, Netherlands
来源:
关键词:
albuminuria;
chronic kidney disease;
dapagliflozin;
eplerenone;
mineralocorticoid receptor antagonist;
sodium-glucose co-transporter 2 inhibitors;
ENDOTHELIAL GLYCOCALYX;
ALBUMINURIA;
OUTCOMES;
D O I:
10.1111/dom.15346
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Aim: Sodium-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.Methods: This 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.Results: The 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)].Conclusions: Dapagliflozin 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.
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页码:576 / 582
页数:7
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