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Submitted: 04 Oct 2025
Revision: 05 Jan 2026
Accepted: 20 Mar 2026
ePublished: 07 Jun 2026
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J Ren Endocrinol. 2026;12: e25204.
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  PDF Download: 1

Review

Sodium-glucose cotransporter 2 inhibitors; revolutionizing diabetic kidney disease management

Afagh Hassanzadeh Rad 1 ORCID logo, Gelayol Chatrnour 2* ORCID logo

1 Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran
2 Independent Researcher, Pennsylvania, United States of America.
*Corresponding Author: Gelayol Chatrnour, Email: Gelayol.ch@gmail.com

Abstract

Diabetic kidney disease (DKD), a leading cause of kidney failure, is driven by hyperglycemia and inflammation. Sodium-glucose cotransporter 2 (SGLT2) inhibitors, initially for type 2 diabetes, transform DKD treatment by reducing glucose reabsorption, easing glomerular pressure, and shortening inflammation. These drugs are safe, with minor risks. Combining with GLP-1 agonists or mineralocorticoid antagonists may boost benefits. In addition, SGLT2 inhibitors slow DKD progression, enhancing patient outcomes. Future studies should refine combination therapies and personalized care.

Citation: Hassanzadeh Rad A, Chatrnour G. Sodium-glucose cotransporter 2 inhibitors; revolutionizing diabetic kidney disease management. J Ren Endocrinol. 2026;12:e25204.
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