Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics

Diabetic kidney disease (DKD) is a prevalent renal complication of diabetes mellitus that ultimately develops into end-stage kidney disease (ESKD) when not managed appropriately. Substantial risk of ESKD remains even with intensive management of hyperglycemia and risk factors of DKD and timely use o...

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Main Authors: Nam Hoon Kim, Nan Hee Kim
Format: Article
Language:English
Published: Korean Diabetes Association 2022-07-01
Series:Diabetes & Metabolism Journal
Subjects:
Online Access:http://e-dmj.org/upload/pdf/dmj-2022-0209.pdf
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author Nam Hoon Kim
Nan Hee Kim
author_facet Nam Hoon Kim
Nan Hee Kim
author_sort Nam Hoon Kim
collection DOAJ
description Diabetic kidney disease (DKD) is a prevalent renal complication of diabetes mellitus that ultimately develops into end-stage kidney disease (ESKD) when not managed appropriately. Substantial risk of ESKD remains even with intensive management of hyperglycemia and risk factors of DKD and timely use of renin-angiotensin-aldosterone inhibitors. Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce hyperglycemia primarily by inhibiting glucose and sodium reabsorption in the renal proximal tubule. Currently, their effects expand to prevent or delay cardiovascular and renal adverse events, even in those without diabetes. In dedicated renal outcome trials, SGLT2 inhibitors significantly reduced the risk of composite renal adverse events, including the development of ESKD or renal replacement therapy, which led to the positioning of SGLT2 inhibitors as the mainstay of chronic kidney disease management. Multiple mechanisms of action of SGLT2 inhibitors, including hemodynamic, metabolic, and anti-inflammatory effects, have been proposed. Restoration of tubuloglomerular feedback is a plausible explanation for the alteration in renal hemodynamics induced by SGLT2 inhibition and for the associated renal benefit. This review discusses the clinical rationale and mechanism related to the protection SGLT2 inhibitors exert on the kidney, focusing on renal hemodynamic effects.
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spelling doaj.art-140d6c860df2499097f3f588176182662022-12-22T00:54:27ZengKorean Diabetes AssociationDiabetes & Metabolism Journal2233-60792233-60872022-07-0146454355110.4093/dmj.2022.02092686Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal HemodynamicsNam Hoon Kim0Nan Hee Kim1Division of Endocrinology and Metabolism, Department of Internal Medicine, Korea University College of Medicine, Seoul, KoreaDivision of Endocrinology and Metabolism, Department of Internal Medicine, Korea University College of Medicine, Seoul, KoreaDiabetic kidney disease (DKD) is a prevalent renal complication of diabetes mellitus that ultimately develops into end-stage kidney disease (ESKD) when not managed appropriately. Substantial risk of ESKD remains even with intensive management of hyperglycemia and risk factors of DKD and timely use of renin-angiotensin-aldosterone inhibitors. Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce hyperglycemia primarily by inhibiting glucose and sodium reabsorption in the renal proximal tubule. Currently, their effects expand to prevent or delay cardiovascular and renal adverse events, even in those without diabetes. In dedicated renal outcome trials, SGLT2 inhibitors significantly reduced the risk of composite renal adverse events, including the development of ESKD or renal replacement therapy, which led to the positioning of SGLT2 inhibitors as the mainstay of chronic kidney disease management. Multiple mechanisms of action of SGLT2 inhibitors, including hemodynamic, metabolic, and anti-inflammatory effects, have been proposed. Restoration of tubuloglomerular feedback is a plausible explanation for the alteration in renal hemodynamics induced by SGLT2 inhibition and for the associated renal benefit. This review discusses the clinical rationale and mechanism related to the protection SGLT2 inhibitors exert on the kidney, focusing on renal hemodynamic effects.http://e-dmj.org/upload/pdf/dmj-2022-0209.pdfdiabetes mellitushemodynamicsrenal insufficiencysodium-glucose transporter 2 inhibitors
spellingShingle Nam Hoon Kim
Nan Hee Kim
Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics
Diabetes & Metabolism Journal
diabetes mellitus
hemodynamics
renal insufficiency
sodium-glucose transporter 2 inhibitors
title Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics
title_full Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics
title_fullStr Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics
title_full_unstemmed Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics
title_short Renoprotective Mechanism of Sodium-Glucose Cotransporter 2 Inhibitors: Focusing on Renal Hemodynamics
title_sort renoprotective mechanism of sodium glucose cotransporter 2 inhibitors focusing on renal hemodynamics
topic diabetes mellitus
hemodynamics
renal insufficiency
sodium-glucose transporter 2 inhibitors
url http://e-dmj.org/upload/pdf/dmj-2022-0209.pdf
work_keys_str_mv AT namhoonkim renoprotectivemechanismofsodiumglucosecotransporter2inhibitorsfocusingonrenalhemodynamics
AT nanheekim renoprotectivemechanismofsodiumglucosecotransporter2inhibitorsfocusingonrenalhemodynamics