Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review

Katrine B Hansen1, Tina Vilsbøll2, Filip K Knop21Department of Clinical Physiology, Glostrup Hospital, University of Copenhagen, Denmark; 2Diabetes Research Division, Department of Internal Medicine F, Gentofte Hospital, University of Copenhagen, DenmarkAbstract: Type 2 diabetes mellitus...

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Main Authors: Knop FK, Hansen K
Format: Article
Language:English
Published: Dove Medical Press 2010-05-01
Series:Diabetes, Metabolic Syndrome and Obesity
Subjects:
Online Access:https://www.dovepress.com/incretin-mimetics-a-novel-therapeutic-option-for-patients-with-type-2--peer-reviewed-article-DMSO
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Hansen K
Knop FK
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description Katrine B Hansen1, Tina Vilsbøll2, Filip K Knop21Department of Clinical Physiology, Glostrup Hospital, University of Copenhagen, Denmark; 2Diabetes Research Division, Department of Internal Medicine F, Gentofte Hospital, University of Copenhagen, DenmarkAbstract: Type 2 diabetes mellitus is a metabolic disease associated with low quality of life and early death. The goal in diabetes treatment is to prevent these outcomes by tight glycemic control and minimizing vascular risk factors. So far, even intensified combination regimen with the traditional antidiabetes agents have failed to obtain these goals. Incretin mimetics are a new class of antidiabetes drugs which involve modulation of the incretin system. They bind to and activate glucagon-like peptide-1 (GLP-1) receptors on pancreatic beta-cells following which insulin secretion and synthesis are initiated. Since the compounds have no insulinotropic activity at lower glucose concentrations the risk of hypoglycemia – a well-known shortcoming of existing antidiabetes treatments – is low. Additionally, incretin mimetics have been shown to be associated with beneficial effects on cardiovascular risk factors such as weight loss, decrease in blood pressure and changes in lipid profile. Current clinical data on the two available incretin mimetics, exenatide and liraglutide, are evaluated in this review, focusing on pharmacology, efficacy, safety and tolerability. The review is built on a systematic PubMed and Medline search for publications with the key words GLP-1 receptor agonist, exenatide, liraglutide and type 2 diabetes mellitus up to January 2009.Keywords: glucagon-like peptide-1 (GLP-1), exenatide, liraglutide, type 2 diabetes
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spelling doaj.art-d61d2987502242fb852f12ca9e997c172023-02-02T10:27:36ZengDove Medical PressDiabetes, Metabolic Syndrome and Obesity1178-70072010-05-01Volume 31551634450Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a reviewKnop FKHansen KKnop FKKatrine B Hansen1, Tina Vilsbøll2, Filip K Knop21Department of Clinical Physiology, Glostrup Hospital, University of Copenhagen, Denmark; 2Diabetes Research Division, Department of Internal Medicine F, Gentofte Hospital, University of Copenhagen, DenmarkAbstract: Type 2 diabetes mellitus is a metabolic disease associated with low quality of life and early death. The goal in diabetes treatment is to prevent these outcomes by tight glycemic control and minimizing vascular risk factors. So far, even intensified combination regimen with the traditional antidiabetes agents have failed to obtain these goals. Incretin mimetics are a new class of antidiabetes drugs which involve modulation of the incretin system. They bind to and activate glucagon-like peptide-1 (GLP-1) receptors on pancreatic beta-cells following which insulin secretion and synthesis are initiated. Since the compounds have no insulinotropic activity at lower glucose concentrations the risk of hypoglycemia – a well-known shortcoming of existing antidiabetes treatments – is low. Additionally, incretin mimetics have been shown to be associated with beneficial effects on cardiovascular risk factors such as weight loss, decrease in blood pressure and changes in lipid profile. Current clinical data on the two available incretin mimetics, exenatide and liraglutide, are evaluated in this review, focusing on pharmacology, efficacy, safety and tolerability. The review is built on a systematic PubMed and Medline search for publications with the key words GLP-1 receptor agonist, exenatide, liraglutide and type 2 diabetes mellitus up to January 2009.Keywords: glucagon-like peptide-1 (GLP-1), exenatide, liraglutide, type 2 diabeteshttps://www.dovepress.com/incretin-mimetics-a-novel-therapeutic-option-for-patients-with-type-2--peer-reviewed-article-DMSOGlucagon-like peptide-1 (GLP-1)exenatideliraglutidetype 2 diabetes.
spellingShingle Knop FK
Hansen K
Knop FK
Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review
Diabetes, Metabolic Syndrome and Obesity
Glucagon-like peptide-1 (GLP-1)
exenatide
liraglutide
type 2 diabetes.
title Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review
title_full Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review
title_fullStr Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review
title_full_unstemmed Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review
title_short Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes – a review
title_sort incretin mimetics a novel therapeutic option for patients with type 2 diabetes ndash a review
topic Glucagon-like peptide-1 (GLP-1)
exenatide
liraglutide
type 2 diabetes.
url https://www.dovepress.com/incretin-mimetics-a-novel-therapeutic-option-for-patients-with-type-2--peer-reviewed-article-DMSO
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