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GLP-1 Receptor Agonists in Diabetic Kidney Disease: From Clinical Outcomes to Mechanisms
- Source :
- Frontiers in Pharmacology, Vol 11 (2020), Frontiers in Pharmacology
- Publication Year :
- 2020
- Publisher :
- Frontiers Media SA, 2020.
-
Abstract
- Diabetic Kidney Disease (DKD) is the leading cause of end stage renal disease (ESRD) worldwide. Glucagon-like peptide 1 receptor agonists (GLP-1RAs) are now widely used in the treatment of patients with type 2 diabetes (T2D). A series of clinical and experimental studies demonstrated that GLP-1RAs have beneficial effects on DKD, independent of their glucose-lowering abilities, which are mediated by natriuresis, anti-inflammatory and anti-oxidative stress properties. Furthermore, GLP-1RAs have been shown to suppress renal fibrosis. Recent clinical trials have demonstrated that GLP-1RAs have beneficial effects on renal outcomes, especially in patients with T2D who are at high risk for CVD. These findings suggest that GLP-1RAs hold great promise in preventing the onset and progression of DKD. However, GLP-1RAs have only been shown to reduce albuminuria, and their ability to reduce progression to ESRD remains to be elucidated. In this review article, we highlight the current understanding of the clinical efficacy and the mechanisms underlying the effects of GLP-1RAs in DKD.
- Subjects :
- 0301 basic medicine
endocrine system
Review
Type 2 diabetes
Bioinformatics
End stage renal disease
Diabetic nephropathy
03 medical and health sciences
0302 clinical medicine
dulaglutide
medicine
Renal fibrosis
Pharmacology (medical)
Glucagon-like peptide 1 receptor
Pharmacology
GLP-1 receptor agonists
liraglutide
semaglutide
business.industry
diabetic nephropathy
Semaglutide
lcsh:RM1-950
digestive, oral, and skin physiology
medicine.disease
diabetic kidney disease
Review article
lcsh:Therapeutics. Pharmacology
030104 developmental biology
030220 oncology & carcinogenesis
Albuminuria
medicine.symptom
business
hormones, hormone substitutes, and hormone antagonists
Subjects
Details
- ISSN :
- 16639812
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Frontiers in Pharmacology
- Accession number :
- edsair.doi.dedup.....16df5bf51cc8abb092ced15e96f5c896
- Full Text :
- https://doi.org/10.3389/fphar.2020.00967