Effects of the SGLT-2 inhibitor dapagliflozin on glomerular and tubular injury markers
- PMID: 29573529
- PMCID: PMC6055757
- DOI: 10.1111/dom.13301
Effects of the SGLT-2 inhibitor dapagliflozin on glomerular and tubular injury markers
Abstract
The mechanisms by which SGLT-2 inhibitors lower albuminuria are incompletely understood. We assessed in a post-hoc analysis of a cross-over trial the effects of the SGLT2 inhibitor dapagliflozin on glomerular markers (IgG to IgG4 and IgG to albumin), tubular markers (urinary KIM-1, NGAL and LFABP) and inflammatory markers (urinary MCP-1 and IL-6) to provide more insight into kidney protective effects. Dapagliflozin decreased albuminuria by 43.9% (95% CI, 30.3%-54.8%) and eGFR by 5.1 (2.0-8.1) mL/min/1.73m2 compared to placebo. Dapagliflozin did not change glomerular charge or size selectivity index compared to placebo. Dapagliflozin decreased urinary KIM-1 excretion by 22.6% (0.3%-39.8%; P = .05) and IL-6 excretion by 23.5% (1.4%-40.6%; P = .04) compared to placebo, whereas no changes in NGAL, LFABP and MCP-1 were observed. During dapagliflozin treatment, changes in albuminuria correlated with changes in eGFR (r = 0.36; P = .05) and KIM-1 (r = 0.39; P = .05). In conclusion, the albuminuria-lowering effect of 6 weeks of dapagliflozin therapy may be the result of decreased intraglomerular pressure or reduced tubular cell injury.
Keywords: KIM-1; MCP-1; SGLT-2; acute kidney injury; dapagliflozin; type 2 diabetes.
© 2018 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.
Conflict of interest statement
C. C. J. D., S. P. and R. T. G. report no conflicts of interest. H. J. L. H. is a consultant for and has received honoraria from AbbVie, Astellas, Astra Zeneca, Boehringer Ingelheim, Fresenius, Janssen and Merck; he has a policy that all honoraria are paid to his employer. D. Z. I. C. has received speaker/consultant honoraria from Boehringer‐Ingelheim, Eli Lilly, AstraZeneca, Sanofi, Merck, Mitsubishi‐Tanabe and Janssen and has received operational funding for clinical trials from Boehringer Ingelheim, Merck and AstraZeneca. G. L. has received lecture fees from Sanofi, Astra Zeneca and Jansen, and has served as a consultant for Abbvie, Sanofi, Novo Nordisk, Astra Zeneca, Boehringer Ingelheim and MSD.
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References
-
- Wanner C, Inzucchi SE, Lachin JM, et al. Empagliflozin and progression of kidney disease in type 2 diabetes. N Engl J Med. 2016;375:323‐334. - PubMed
-
- Neal B, Perkovic V, Mahaffey KW, et al. Canagliflozin and cardiovascular and renal events in type 2 diabetes. N Engl J Med. 2017;377:644‐657. - PubMed
-
- Cherney DZ, Perkins BA, Soleymanlou N, et al. Renal hemodynamic effect of sodium‐glucose cotransporter 2 inhibition in patients with type 1 diabetes mellitus. Circulation. 2014;129:587‐597. - PubMed
-
- Heerspink HJ, Perkins BA, Fitchett DH, Husain M, Cherney DZ. Sodium glucose cotransporter 2 inhibitors in the treatment of diabetes mellitus: cardiovascular and kidney effects, potential mechanisms, and clinical applications. Circulation. 2016;34:752‐772. - PubMed
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