Abstract |
Worldwide, an estimated 200 million people have chronic kidney disease (CKD), whose most common causes include hypertension, arteriosclerosis, and diabetes. About 40% of patients with diabetes develop CKD and intensive blood glucose control through pharmacological intervention can delay CKD progression. Standard therapies for the treatment of type 2 diabetes mellitus include metformin, sulfonylureas, meglitinides, thiazolidinediones, and insulin. While these drugs have an important role in the management of type 2 diabetes, only the thiazolidinedione pioglitazone can be used across the spectrum of CKD (stages 2-5) and without dose adjustment. Newer therapies, particularly dipeptidyl peptidase-IV inhibitors, glucagon-like peptide-1 receptor agonists, and sodium- glucose cotransporter-2 inhibitors, are increasingly being used in the treatment of type 2 diabetes; however, a major consideration is whether these newer therapies can also be used safely and effectively across the spectrum of renal impairment.
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Authors | Luca Di Lullo, Michela Mangano, Claudio Ronco, Vincenzo Barbera, Antonio De Pascalis, Antonio Bellasi, Domenico Russo, Biagio Di Iorio, Mario Cozzolino |
Journal | Diabetes & metabolic syndrome
(Diabetes Metab Syndr)
Vol. 11 Suppl 1
Pg. S295-S305
(Nov 2017)
ISSN: 1878-0334 [Electronic] Netherlands |
PMID | 28292575
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2017 Diabetes India. Published by Elsevier Ltd. All rights reserved. |
Chemical References |
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Topics |
- Administration, Oral
- Animals
- Diabetes Mellitus, Type 2
(drug therapy, etiology)
- Humans
- Hypoglycemic Agents
(administration & dosage)
- Prognosis
- Renal Insufficiency, Chronic
(complications)
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