Pharmacotherapy of type 2 diabetes: An update and future directions
- PMID: 36240884
- DOI: 10.1016/j.metabol.2022.155332
Pharmacotherapy of type 2 diabetes: An update and future directions
Abstract
Type 2 diabetes (T2D) is a widely prevalent disease with substantial economic and social impact for which multiple conventional and novel pharmacotherapies are currently available; however, the landscape of T2D treatment is constantly changing as new therapies emerge and the understanding of currently available agents deepens. This review aims to provide an updated summary of the pharmacotherapeutic approach to T2D. Each class of agents is presented by mechanism of action, details of administration, side effect profile, cost, and use in certain populations including heart failure, non-alcoholic fatty liver disease, obesity, chronic kidney disease, and older individuals. We also review targets of novel therapeutic T2D agent development. Finally, we outline an up-to-date treatment approach that starts with identification of an individualized goal for glycemic control then selection, initiation, and further intensification of a personalized therapeutic plan for T2D.
Keywords: Amylin analogs; Biguanides; Diabetes mellitus; Glucagon-like peptide-1 receptor agonists; Meglitinides; Pharmacotherapy; Sodium-glucose cotransporter 2 inhibitors; Sulfonylureas; Thiazolidinediones; α-Glucosidase inhibitors.
Copyright © 2022 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest NK has given talks, attended conferences and participated in trials sponsored by Amgen, Astra Zeneca, Boehringer Ingelheim, Elpen, Menarini, Novartis, Novo Nordisk, Sanofi, Servier, Vianex and Viatris. None is related to the work presented herein. CSM reports (for last year) grants through his institution from Merck, has been a shareholder of and has received grants through his Institution and personal consulting fees from Coherus Inc. and AltrixBio, reports personal consulting fees and support with research reagents from Ansh Inc., collaborative research support from LabCorp Inc., reports personal consulting fees from Amgen, Corcept, Regeneron, Madrigal, 89Bio, reports travel support and fees from TMIOA, Elsevier, College Internationale Researche Servier and the Cardio Metabolic Health Conference. None is related to the work presented herein. AD, NR, CB, AF and ES have nothing to declare.
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