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Erschienen in: Reactions Weekly 1/2013

01.07.2013 | News item

Debate continues over safety of incretin mimetics

verfasst von: Lesley Scott

Erschienen in: Reactions Weekly | Ausgabe 1/2013

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Abstract

Incretin mimetics, which include glucagon-like peptide (GLP)-1 receptor agonists (such as exenatide and liraglutide), and dipeptidylpeptidase (DPP)-4 inhibitors (such as alogliptin and sitagliptin), are considered a major advancement in the management of type 2 diabetes, particularly given their dual mechanisms of action, in enhancing insulin secretion and suppressing glucagon, to reduce blood glucose; their low propensity to cause hypoglycaemia; and their beneficial effects on bodyweight. However, of recent times, there has been considerable debate and controversy regarding the potential for incretin mimetics to cause pancreatitis, pancreatic cancer and thyroid cancer.
Fußnoten
1
see Reactions 1442 p3; 801161308
 
2
see Reactions 1450 p4; 801161350
 
Literatur
4.
Zurück zum Zitat Novo Nordisk. Novo Nordisk - Victoza(Rm) safety profile further supported atscientific workshop on pancreatitis, diabetes and pancreatic cancer. Media Release : 13 Jun 2013. Available from: URL: http://www.novonordisk.com. Novo Nordisk. Novo Nordisk - Victoza(Rm) safety profile further supported atscientific workshop on pancreatitis, diabetes and pancreatic cancer. Media Release : 13 Jun 2013. Available from: URL: http://​www.​novonordisk.​com.
5.
Zurück zum Zitat American Diabetes Association. American Diabetes Association Calls for Independent Review of Incretin Therapy. Media Release : 10 Jun 2013. Available from: URL: http://www.diabetes.org. American Diabetes Association. American Diabetes Association Calls for Independent Review of Incretin Therapy. Media Release : 10 Jun 2013. Available from: URL: http://​www.​diabetes.​org.
Metadaten
Titel
Debate continues over safety of incretin mimetics
verfasst von
Lesley Scott
Publikationsdatum
01.07.2013
Verlag
Springer International Publishing
Erschienen in
Reactions Weekly / Ausgabe 1/2013
Print ISSN: 0114-9954
Elektronische ISSN: 1179-2051
DOI
https://doi.org/10.1007/s40278-013-4523-6

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