English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Zendy Plus

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Zendy Tools

Zendy Open

Obective  Glucagon‐like peptide‐1 (GLP‐1) receptor agonists are indicated for treatment of type 2 diabetes since they mimic the actions of native GLP‐1 on pancreatic islet cells, stimulating insulin release, while inhibiting glucagon release, in a glucose‐dependent manner. The observation of weight loss has led to exploration of their potential as antiobesity agents, with liraglutide 3.0 mg day −1  approved for weight management in the US on December 23, 2014, and in the EU on March 23, 2015. This review examines the potential nonglycemic effects of GLP‐1 receptor agonists.    Methods  A literature search was conducted to identify preclinical and clinical evidence on nonglycemic effects of GLP‐1 receptor agonists.    Results  GLP‐1 receptors are distributed widely in a number of tissues in humans, and their effects are not limited to the well‐recognized effects on glycemia. Nonglycemic effects include weight loss, which is perhaps the most widely recognized nonglycemic effect. In addition, effects on the cardiovascular, neurologic, and renal systems and on taste perception may occur independently of weight loss.    Conclusions  GLP‐1 receptor agonists may provide other nonglycemic clinical effects besides weight loss. Understanding these effects is important for prescribers in using GLP‐1 receptor agonists for diabetic patients, but also if approved for chronic weight management.

GLP ‐1 receptor agonists: Nonglycemic clinical effects in weight loss and beyond