
Incretin‐based therapies
Author(s) -
STONEHOUSE Anthony H.,
DARSOW Tamara,
MAGGS David G.
Publication year - 2012
Publication title -
journal of diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.949
H-Index - 43
eISSN - 1753-0407
pISSN - 1753-0393
DOI - 10.1111/j.1753-0407.2011.00143.x
Subject(s) - incretin , medicine , glycemic , diabetes mellitus , type 2 diabetes , glucose homeostasis , hypoglycemia , glucagon like peptide 1 , postprandial , dipeptidyl peptidase 4 , endocrinology , bioinformatics , insulin resistance , biology
Incretin‐based therapies have established a foothold in the diabetes armamentarium through the introduction of oral dipeptidyl peptidase‐4 inhibitors and the injectable class, the glucagon‐like peptide‐1 receptor agonists. In 2009, the American Diabetes Association and European Association for the Study of Diabetes authored a revised consensus algorithm for the initiation and adjustment of therapy in Type 2 diabetes (T2D). The revised algorithm accounts for the entry of incretin‐based therapies into common clinical practice, especially where control of body weight and hypoglycemia are concerns. The gut‐borne incretin hormones have powerful effects on glucose homeostasis, particularly in the postprandial period, when approximately two‐thirds of the β‐cell response to a given meal is due to the incretin effect. There is also evidence that the incretin effect is attenuated in patients with T2D, whereby the β‐cell becomes less responsive to incretin signals. The foundation of incretin‐based therapies is to target this previously unrecognized feature of diabetes pathophysiology, resulting in sustained improvements in glycemic control and improved body weight control. In addition, emerging evidence suggests that incretin‐based therapies may have a positive impact on inflammation, cardiovascular and hepatic health, sleep, and the central nervous system. In the present article, we discuss the attributes of current and near‐future incretin‐based therapies.