Cargando…

Review of sitagliptin phosphate: a novel treatment for type 2 diabetes

Sitagliptin (Januvia®, Merck Pharmaceuticals) is a dipeptidyl-peptidase inhibitor (DPP-4 inhibitor) that has recently been approved for the therapy of type 2 diabetes. Like other DPP-4 inhibitors its action is mediated by increasing levels of the incretin hormones glucagon-like peptide-1 (GLP-1) and...

Descripción completa

Detalles Bibliográficos
Autor principal: Gallwitz, Baptist
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1994027/
https://www.ncbi.nlm.nih.gov/pubmed/17580730
_version_ 1782135471754706944
author Gallwitz, Baptist
author_facet Gallwitz, Baptist
author_sort Gallwitz, Baptist
collection PubMed
description Sitagliptin (Januvia®, Merck Pharmaceuticals) is a dipeptidyl-peptidase inhibitor (DPP-4 inhibitor) that has recently been approved for the therapy of type 2 diabetes. Like other DPP-4 inhibitors its action is mediated by increasing levels of the incretin hormones glucagon-like peptide-1 (GLP-1) and gastric inhibitory polypeptide (GIP). Sitagliptin is effective in lowering HbA1c, and fasting as well as postprandial glucose in monotherapy and in combination with other oral antidiabetic agents. It stimulates insulin secretion when hyperglycemia is present and inhibits glucagon secretion. In clinical studies it is weight neutral. This article gives an overview of the mechanism of action, the pharmacology, and the clinical efficacy and safety of sitagliptin in type 2 diabetes therapy.
format Text
id pubmed-1994027
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-19940272008-03-06 Review of sitagliptin phosphate: a novel treatment for type 2 diabetes Gallwitz, Baptist Vasc Health Risk Manag Review Sitagliptin (Januvia®, Merck Pharmaceuticals) is a dipeptidyl-peptidase inhibitor (DPP-4 inhibitor) that has recently been approved for the therapy of type 2 diabetes. Like other DPP-4 inhibitors its action is mediated by increasing levels of the incretin hormones glucagon-like peptide-1 (GLP-1) and gastric inhibitory polypeptide (GIP). Sitagliptin is effective in lowering HbA1c, and fasting as well as postprandial glucose in monotherapy and in combination with other oral antidiabetic agents. It stimulates insulin secretion when hyperglycemia is present and inhibits glucagon secretion. In clinical studies it is weight neutral. This article gives an overview of the mechanism of action, the pharmacology, and the clinical efficacy and safety of sitagliptin in type 2 diabetes therapy. Dove Medical Press 2007-04 /pmc/articles/PMC1994027/ /pubmed/17580730 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Review
Gallwitz, Baptist
Review of sitagliptin phosphate: a novel treatment for type 2 diabetes
title Review of sitagliptin phosphate: a novel treatment for type 2 diabetes
title_full Review of sitagliptin phosphate: a novel treatment for type 2 diabetes
title_fullStr Review of sitagliptin phosphate: a novel treatment for type 2 diabetes
title_full_unstemmed Review of sitagliptin phosphate: a novel treatment for type 2 diabetes
title_short Review of sitagliptin phosphate: a novel treatment for type 2 diabetes
title_sort review of sitagliptin phosphate: a novel treatment for type 2 diabetes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1994027/
https://www.ncbi.nlm.nih.gov/pubmed/17580730
work_keys_str_mv AT gallwitzbaptist reviewofsitagliptinphosphateanoveltreatmentfortype2diabetes