

Author: Sonnett Travis E Robinson Jennifer D Bowen Kurt A
Publisher: Future Medicine
ISSN: 1475-0708
Source: Therapy, Vol.8, Iss.2, 2011-03, pp. : 143-152
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Abstract
Several incretin therapies have been approved by the US FDA and/or the European Union for treatment of Type 2 diabetes mellitus (T2DM), either as monotherapy or in conjunction with diet, exercise and other T2DM therapies. Incretin-based therapies, specifically glucagon-like peptide-1 agonists, have been reported to offer a unique mechanism to lower hemoglobin A1c levels by 0.4––1.1%, as demonstrated in clinical trials, and as a secondary effect reduce weight by 1––4 kg. Dipeptidyl peptidase-4 inhibitors also offer a new mechanism to reduce hemoglobin A1c levels by 0.3––1.9%, as seen in clinical trials; weight loss, however, has been reported as variable. Given the projected increase in obesity and diabetes, as well as the growing evidence linking obesity and development of T2DM, incretin-based therapies may offer a future first-line agent to fight both rising sugars and rising weight.
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