Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes
Glucagon-like peptide-1 (GLP-1) receptor agonists (GLP-1RAs) are a class of antidiabetic drugs developed over the past 15 years. GLP-1, a gastrointestinal peptide hormone that contributes to the postprandial “incretin effect”, stimulates glucose-dependent insulin secretion. The i...
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Endocrinology Research Centre
2017
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oai:doaj.org-article:a1353861504246f5877ed418350e4d422021-11-14T09:00:21ZEvolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes2072-03512072-037810.14341/DM8804https://doaj.org/article/a1353861504246f5877ed418350e4d422017-10-01T00:00:00Zhttps://www.dia-endojournals.ru/jour/article/view/8804https://doaj.org/toc/2072-0351https://doaj.org/toc/2072-0378Glucagon-like peptide-1 (GLP-1) receptor agonists (GLP-1RAs) are a class of antidiabetic drugs developed over the past 15 years. GLP-1, a gastrointestinal peptide hormone that contributes to the postprandial “incretin effect”, stimulates glucose-dependent insulin secretion. The incretin effect is greatly diminished in type 2 diabetes, but can be restored by GLP-1RAs. These drugs also exert other GLP-1 effects, including reducing glucagon secretion, delaying gastric emptying, reducing food intake, improving cardiac ventricular function, and lowering blood pressure. Short-acting GLP-1RAs are administered once daily (lixisenatide) or twice daily (exenatide); long-acting GLP 1RAs are administered once daily (liraglutide) or once weekly (slow-release exenatide, dulaglutide, albiglutide). All GLP-1RAs significantly reduce glycated hemoglobin (HbA1c) in patients with type 2 diabetes whose glycemic control is inadequate with oral antidiabetic drugs. Compared with other antidiabetic medications, GLP-1RAs provide better glycemic control with the additional benefit of weight loss. Within this class, long-acting GLP-1RAs are more efficacious than short-acting GLP-1RAs, with similar or lower risk of hypoglycemia and lower incidence of gastrointestinal adverse effects. Head-to-head trials and a network meta-analysis suggest that once daily liraglutide is the most effective GLP-1RA in reducing HbA1c. Dulaglutide is the only once-weekly GLP 1RA demonstrated to be noninferior to liraglutide. The once-weekly GLP-1RAs offer additional advantages to patients, including fewer injections and easy-to-use, single-dose pen devices. Despite the relatively recent development of GLP-1RAs, international diabetes guidelines recognize the benefits of this class of drugs and recommend them as a treatment option for patients with type 2 diabetes.Gagik R. GalstyanEvgeniya A. KarataevaEkaterina A. YudovichEndocrinology Research Centrearticlediabetes mellitus, type 2glucagon-like peptide-1glucagon-like peptide-1 receptorhypoglycemic agentsincretinsNutritional diseases. Deficiency diseasesRC620-627ENRUСахарный диабет, Vol 20, Iss 4, Pp 286-298 (2017) |
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diabetes mellitus, type 2 glucagon-like peptide-1 glucagon-like peptide-1 receptor hypoglycemic agents incretins Nutritional diseases. Deficiency diseases RC620-627 |
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diabetes mellitus, type 2 glucagon-like peptide-1 glucagon-like peptide-1 receptor hypoglycemic agents incretins Nutritional diseases. Deficiency diseases RC620-627 Gagik R. Galstyan Evgeniya A. Karataeva Ekaterina A. Yudovich Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
description |
Glucagon-like peptide-1 (GLP-1) receptor agonists (GLP-1RAs) are a class of antidiabetic drugs developed over the past 15 years. GLP-1, a gastrointestinal peptide hormone that contributes to the postprandial “incretin effect”, stimulates glucose-dependent insulin secretion. The incretin effect is greatly diminished in type 2 diabetes, but can be restored by GLP-1RAs. These drugs also exert other GLP-1 effects, including reducing glucagon secretion, delaying gastric emptying, reducing food intake, improving cardiac ventricular function, and lowering blood pressure. Short-acting GLP-1RAs are administered once daily (lixisenatide) or twice daily (exenatide); long-acting GLP 1RAs are administered once daily (liraglutide) or once weekly (slow-release exenatide, dulaglutide, albiglutide). All GLP-1RAs significantly reduce glycated hemoglobin (HbA1c) in patients with type 2 diabetes whose glycemic control is inadequate with oral antidiabetic drugs. Compared with other antidiabetic medications, GLP-1RAs provide better glycemic control with the additional benefit of weight loss. Within this class, long-acting GLP-1RAs are more efficacious than short-acting GLP-1RAs, with similar or lower risk of hypoglycemia and lower incidence of gastrointestinal adverse effects. Head-to-head trials and a network meta-analysis suggest that once daily liraglutide is the most effective GLP-1RA in reducing HbA1c. Dulaglutide is the only once-weekly GLP 1RA demonstrated to be noninferior to liraglutide. The once-weekly GLP-1RAs offer additional advantages to patients, including fewer injections and easy-to-use, single-dose pen devices. Despite the relatively recent development of GLP-1RAs, international diabetes guidelines recognize the benefits of this class of drugs and recommend them as a treatment option for patients with type 2 diabetes. |
format |
article |
author |
Gagik R. Galstyan Evgeniya A. Karataeva Ekaterina A. Yudovich |
author_facet |
Gagik R. Galstyan Evgeniya A. Karataeva Ekaterina A. Yudovich |
author_sort |
Gagik R. Galstyan |
title |
Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
title_short |
Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
title_full |
Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
title_fullStr |
Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
title_full_unstemmed |
Evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
title_sort |
evolution of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes |
publisher |
Endocrinology Research Centre |
publishDate |
2017 |
url |
https://doaj.org/article/a1353861504246f5877ed418350e4d42 |
work_keys_str_mv |
AT gagikrgalstyan evolutionofglucagonlikepeptide1receptoragonistsforthetreatmentoftype2diabetes AT evgeniyaakarataeva evolutionofglucagonlikepeptide1receptoragonistsforthetreatmentoftype2diabetes AT ekaterinaayudovich evolutionofglucagonlikepeptide1receptoragonistsforthetreatmentoftype2diabetes |
_version_ |
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