Literature DB >> 26587691

An overview of new GLP-1 receptor agonists for type 2 diabetes.

Brian Tomlinson1,2, Miao Hu2, Yuzhen Zhang1, Paul Chan3, Zhong-Min Liu4.   

Abstract

INTRODUCTION: The increasing prevalence of type 2 diabetes mellitus (T2DM) and the eventual need for multiple medications in most patients stimulated the development of new drug classes to reduce plasma glucose levels. The GLP-1 receptor agonists (GLP-1RAs) are established as an option for treatment of T2DM after metformin. They are also effective in reducing body weight but current GLP-1RAs have to be given by subcutaneous injection daily or once weekly. AREAS COVERED: This review focuses on the new GLP-1RAs currently undergoing development, some of which require less frequent subcutaneous administration and others that are being developed in oral formulations that may favor patient adherence. EXPERT OPINION: The new GLP-1RAs may have the benefit of requiring less frequent subcutaneous dosing or being active by oral administration. However, cardiovascular outcome trials have shown that DPP4 inhibitors are neutral for cardiovascular events and the first cardiovascular outcome trial with lixisenatide reported similar results, whereas the trial with the SGLT2 inhibitor empagliflozin showed a reduction in cardiovascular events. These findings in patients with high cardiovascular risk may favor the use of SGLT2 inhibitors as a second line treatment after metformin but there should still be an important role for novel GLP-1RAs, especially when weight reduction is required.

Entities:  

Keywords:  Efpeglenatide; GLP-1; GLP-1 receptor agonist; glymera; semaglutide; type 2 diabetes mellitus

Mesh:

Substances:

Year:  2015        PMID: 26587691     DOI: 10.1517/13543784.2016.1123249

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  6 in total

1.  Xenopus-derived glucagon-like peptide-1 and polyethylene-glycosylated glucagon-like peptide-1 receptor agonists: long-acting hypoglycaemic and insulinotropic activities with potential therapeutic utilities.

Authors:  Jing Han; Yingying Fei; Feng Zhou; Xinyu Chen; Ying Zhang; Lin Liu; Junjie Fu
Journal:  Br J Pharmacol       Date:  2018-01-08       Impact factor: 8.739

Review 2.  Recent Advances in GLP-1 Receptor Agonists for Use in Diabetes Mellitus.

Authors:  Dominic N McBrayer; Yftah Tal-Gan
Journal:  Drug Dev Res       Date:  2017-08-08       Impact factor: 4.360

3.  Complement 1q-like-3 protein inhibits insulin secretion from pancreatic β-cells via the cell adhesion G protein-coupled receptor BAI3.

Authors:  Rajesh Gupta; Dan C Nguyen; Michael D Schaid; Xia Lei; Appakalai N Balamurugan; G William Wong; Jeong-A Kim; James E Koltes; Michelle E Kimple; Sushant Bhatnagar
Journal:  J Biol Chem       Date:  2018-09-18       Impact factor: 5.157

4.  ZB-16, a Novel GPR119 Agonist, Relieves the Severity of Streptozotocin-Nicotinamide-Induced Diabetes in Rats.

Authors:  Ivan N Tyurenkov; Denis V Kurkin; Dmitry A Bakulin; Elena V Volotova; Mikhail A Chafeev; Alexey V Smirnov; Evgeny I Morkovin
Journal:  Front Endocrinol (Lausanne)       Date:  2017-07-07       Impact factor: 5.555

5.  Liraglutide Treatment Reduces Endothelial Endoplasmic Reticulum Stress and Insulin Resistance in Patients With Diabetes Mellitus.

Authors:  Rosa Bretón-Romero; Robert M Weisbrod; Bihua Feng; Monika Holbrook; Darae Ko; Mary M Stathos; Ji-Yao Zhang; Jessica L Fetterman; Naomi M Hamburg
Journal:  J Am Heart Assoc       Date:  2018-09-18       Impact factor: 5.501

6.  Relationship Between Oral Semaglutide Tablet Erosion and Pharmacokinetics: A Pharmacoscintigraphic Study.

Authors:  Tine A Baekdal; Morten Donsmark; Marie-Louise Hartoft-Nielsen; Flemming L Søndergaard; Alyson Connor
Journal:  Clin Pharmacol Drug Dev       Date:  2021-03-22
  6 in total

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