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Updated: Jul 29, 2025

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
Published on: May 2, 2025
Nephroprotective Properties of Antidiabetic Drugs
Christian Gerdes1, Nicolle Müller1, Gunter Wolf1
1Department of Internal Medicine III, University Hospital Jena, D-07747 Jena, Germany.
Insights
Novel antidiabetic drugs, sodium-glucose cotransporter 2 inhibitors (SGLT2-I) and glucagon-like peptide 1 receptor agonists (GLP1-RA), offer significant kidney protection in diabetes. These drugs slow chronic kidney disease progression and reduce cardiovascular risks.
Area of Science:
- Nephrology
- Endocrinology
- Cardiology
Background:
- Chronic kidney disease (CKD) significantly increases morbidity and mortality, particularly cardiovascular (CV) causes, especially in patients with diabetes mellitus (DM).
- Diabetes itself elevates CV risk and exacerbates CKD development and progression.
- Effective management of CKD, including slowing its progression, is crucial alongside glycemic control in diabetic patients.
Purpose of the Study:
- To review the nephroprotective effects of novel antidiabetic medications.
- To discuss the role of sodium-glucose cotransporter 2 inhibitors (SGLT2-I) and glucagon-like peptide 1 receptor agonists (GLP1-RA) in managing CKD in patients with and without DM.
- To highlight current guideline recommendations for using these agents.
Main Methods:
- Review of cardiovascular outcome trials and clinical guidelines.
- Analysis of data on the impact of SGLT2-I and GLP1-RA on renal outcomes.
- Discussion of nephroprotective properties of other antidiabetic agents.
Main Results:
- GLP1-RA demonstrated a reduction in macroalbuminuria risk.
- SGLT2-I showed a reduced risk of declining glomerular filtration rate (GFR) and have shown benefits even in non-diabetic individuals.
- Both SGLT2-I and GLP1-RA are recommended for patients with DM, CKD, and/or increased CV risk.
Conclusions:
- Novel antidiabetic drugs, SGLT2-I and GLP1-RA, provide significant kidney protection beyond glucose lowering.
- These agents are vital in managing CKD progression and cardiovascular risk in diabetic patients.
- The review also considers nephroprotective aspects of other antidiabetic medications.
Abstract:
Chronic kidney disease (CKD) is associated with increased morbidity and mortality, especially from cardiovascular (CV) causes, and especially in people with diabetes mellitus (DM). Already the presence of DM increases CV risk and potentiates the risk of CKD. Therefore, besides glycemic control, prevention and treatment of CKD to slow its progression are of clinical importance. A significant nephroprotective effect of novel antidiabetic drugs, namely sodium-glucose cotransporter 2 inhibitors (SGLT2-I) and glucagon-like peptide 1 receptor agonists (GLP1-RA), has been shown on top of their glucose-lowering effects and was confirmed in cardiovascular outcome trials. GLP1-RA mainly reduced the risk of macroalbuminuria, whereas SGLT2-I were also associated with a lower risk of declining glomerular filtration rate (GFR) over time. The nephroprotective effects of SGLT2-I are also evident in people without DM. According to current guidelines, SGLT2-I and/or GLP1-RA are recommended for people with DM who have chronic kidney disease and/or increased cardiovascular risk. However, other antidiabetic drugs offer nephroprotective properties, which will also be discussed in this review.
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