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Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond

The therapeutic benefits of the incretin hormone, glucagon-like peptide 1 (GLP1), for people with type 2 diabetes and/or obesity, are now firmly established. The evidence-base arising from head-to-head comparative effectiveness studies in people with type 2 diabetes, as well as the recommendations b...

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Autores principales: Viljoen, Adie, Bain, Stephen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008669/
https://www.ncbi.nlm.nih.gov/pubmed/36740965
http://dx.doi.org/10.3803/EnM.2022.1642
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author Viljoen, Adie
Bain, Stephen C.
author_facet Viljoen, Adie
Bain, Stephen C.
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description The therapeutic benefits of the incretin hormone, glucagon-like peptide 1 (GLP1), for people with type 2 diabetes and/or obesity, are now firmly established. The evidence-base arising from head-to-head comparative effectiveness studies in people with type 2 diabetes, as well as the recommendations by professional guidelines suggest that GLP1 receptor agonists should replace more traditional treatment options such as sulfonylureas and dipeptidyl-peptidase 4 (DPP4) inhibitors. Furthermore, their benefits in reducing cardiovascular events in people with type 2 diabetes beyond improvements in glycaemic control has led to numerous clinical trials seeking to translate this benefit beyond type 2 diabetes. Following early trial results their therapeutic benefit is currently being tested in other conditions including fatty liver disease, kidney disease, and Alzheimer’s disease.
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spelling pubmed-100086692023-03-13 Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond Viljoen, Adie Bain, Stephen C. Endocrinol Metab (Seoul) Review Article The therapeutic benefits of the incretin hormone, glucagon-like peptide 1 (GLP1), for people with type 2 diabetes and/or obesity, are now firmly established. The evidence-base arising from head-to-head comparative effectiveness studies in people with type 2 diabetes, as well as the recommendations by professional guidelines suggest that GLP1 receptor agonists should replace more traditional treatment options such as sulfonylureas and dipeptidyl-peptidase 4 (DPP4) inhibitors. Furthermore, their benefits in reducing cardiovascular events in people with type 2 diabetes beyond improvements in glycaemic control has led to numerous clinical trials seeking to translate this benefit beyond type 2 diabetes. Following early trial results their therapeutic benefit is currently being tested in other conditions including fatty liver disease, kidney disease, and Alzheimer’s disease. Korean Endocrine Society 2023-02 2023-02-06 /pmc/articles/PMC10008669/ /pubmed/36740965 http://dx.doi.org/10.3803/EnM.2022.1642 Text en Copyright © 2023 Korean Endocrine Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Viljoen, Adie
Bain, Stephen C.
Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond
title Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond
title_full Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond
title_fullStr Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond
title_full_unstemmed Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond
title_short Glucagon-Like Peptide 1 Therapy: From Discovery to Type 2 Diabetes and Beyond
title_sort glucagon-like peptide 1 therapy: from discovery to type 2 diabetes and beyond
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008669/
https://www.ncbi.nlm.nih.gov/pubmed/36740965
http://dx.doi.org/10.3803/EnM.2022.1642
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