Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies

John Gerich Department of Medicine, Endocrine/Metabolism Division, University of Rochester School of Medicine, Rochester, NY, USA Abstract: Postprandial plasma glucose concentrations are an important contributor to glycemic control. There is evidence suggesting that postprandial hyperglycemia may be...

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Main Author: Gerich J
Format: Article
Language:English
Published: Dove Medical Press 2013-12-01
Series:International Journal of General Medicine
Online Access:http://www.dovepress.com/pathogenesis-and-management-of-postprandial-hyperglycemia-role-of-incr-a15174
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author Gerich J
author_facet Gerich J
author_sort Gerich J
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description John Gerich Department of Medicine, Endocrine/Metabolism Division, University of Rochester School of Medicine, Rochester, NY, USA Abstract: Postprandial plasma glucose concentrations are an important contributor to glycemic control. There is evidence suggesting that postprandial hyperglycemia may be an independent risk factor for cardiovascular disease. Glucagon-like peptide-1 (GLP-1) receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors are antidiabetic agents that predominantly reduce postprandial plasma glucose levels. DPP-4 inhibitors are associated with fewer gastrointestinal side effects than GLP-1 receptor agonists and are administered orally, unlike GLP-1 analogs, which are administered as subcutaneous injections. GLP-1 receptor agonists are somewhat more effective than DPP-4 inhibitors in reducing postprandial plasma glucose and are usually associated with significant weight loss. For these reasons, GLP-1 receptor agonists are generally preferred over DPP-4 inhibitors as part of combination treatment regimens in patients with glycated hemoglobin levels above 8.0%. This article reviews the pathogenesis of postprandial hyperglycemia, the mechanisms by which GLP-1 receptor agonists and DPP-4 inhibitors reduce postprandial plasma glucose concentrations, and the results of recent clinical trials (ie, published 2008 to October 2012) that evaluated the effects of these agents on postprandial plasma glucose levels when evaluated as monotherapy compared with placebo or as add-on therapy to metformin, a sulfonylurea, or insulin. Findings from recent clinical studies suggest that both GLP-1 receptor agonists and DPP-4 inhibitors could become valuable treatment options for optimizing glycemic control in patients unable to achieve glycated hemoglobin goals on basal insulin, with the added benefits of weight loss and a low risk of hypoglycemia. Keywords: postprandial hyperglycemia, glucagon-like peptide-1, dipeptidyl peptidase-4, type 2 diabetes mellitus
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spelling doaj.art-5ab944dacee94f1f87c071578992617c2022-12-22T03:15:29ZengDove Medical PressInternational Journal of General Medicine1178-70742013-12-012013default877895Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapiesGerich JJohn Gerich Department of Medicine, Endocrine/Metabolism Division, University of Rochester School of Medicine, Rochester, NY, USA Abstract: Postprandial plasma glucose concentrations are an important contributor to glycemic control. There is evidence suggesting that postprandial hyperglycemia may be an independent risk factor for cardiovascular disease. Glucagon-like peptide-1 (GLP-1) receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors are antidiabetic agents that predominantly reduce postprandial plasma glucose levels. DPP-4 inhibitors are associated with fewer gastrointestinal side effects than GLP-1 receptor agonists and are administered orally, unlike GLP-1 analogs, which are administered as subcutaneous injections. GLP-1 receptor agonists are somewhat more effective than DPP-4 inhibitors in reducing postprandial plasma glucose and are usually associated with significant weight loss. For these reasons, GLP-1 receptor agonists are generally preferred over DPP-4 inhibitors as part of combination treatment regimens in patients with glycated hemoglobin levels above 8.0%. This article reviews the pathogenesis of postprandial hyperglycemia, the mechanisms by which GLP-1 receptor agonists and DPP-4 inhibitors reduce postprandial plasma glucose concentrations, and the results of recent clinical trials (ie, published 2008 to October 2012) that evaluated the effects of these agents on postprandial plasma glucose levels when evaluated as monotherapy compared with placebo or as add-on therapy to metformin, a sulfonylurea, or insulin. Findings from recent clinical studies suggest that both GLP-1 receptor agonists and DPP-4 inhibitors could become valuable treatment options for optimizing glycemic control in patients unable to achieve glycated hemoglobin goals on basal insulin, with the added benefits of weight loss and a low risk of hypoglycemia. Keywords: postprandial hyperglycemia, glucagon-like peptide-1, dipeptidyl peptidase-4, type 2 diabetes mellitushttp://www.dovepress.com/pathogenesis-and-management-of-postprandial-hyperglycemia-role-of-incr-a15174
spellingShingle Gerich J
Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies
International Journal of General Medicine
title Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies
title_full Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies
title_fullStr Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies
title_full_unstemmed Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies
title_short Pathogenesis and management of postprandial hyperglycemia: role of incretin-based therapies
title_sort pathogenesis and management of postprandial hyperglycemia role of incretin based therapies
url http://www.dovepress.com/pathogenesis-and-management-of-postprandial-hyperglycemia-role-of-incr-a15174
work_keys_str_mv AT gerichj pathogenesisandmanagementofpostprandialhyperglycemiaroleofincretinbasedtherapies