| Literature DB >> 28292575 |
Luca Di Lullo1, Michela Mangano2, Claudio Ronco3, Vincenzo Barbera4, Antonio De Pascalis5, Antonio Bellasi6, Domenico Russo7, Biagio Di Iorio8, Mario Cozzolino2.
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.Entities:
Keywords: Chronic kidney disease; DPP-IV inhibitors; Diabetic nephropathy; GLP-1 agonists; SGLT-2 inhibitors
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Year: 2017 PMID: 28292575 DOI: 10.1016/j.dsx.2017.03.005
Source DB: PubMed Journal: Diabetes Metab Syndr ISSN: 1871-4021