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Canagliflozin: a novel treatment option for type 2 diabetes
Type 2 diabetes continues to be a challenging disease to manage. The addition of new agents with a positive risk–benefit ratio could potentially assist clinicians and patients in achieving adequate diabetes control. Canagliflozin, the first sodium-glucose cotransporter 2 inhibitor presently availabl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840773/ https://www.ncbi.nlm.nih.gov/pubmed/24285921 http://dx.doi.org/10.2147/DDDT.S48937 |
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author | Dietrich, Eric Powell, Jason Taylor, James R |
author_facet | Dietrich, Eric Powell, Jason Taylor, James R |
author_sort | Dietrich, Eric |
collection | PubMed |
description | Type 2 diabetes continues to be a challenging disease to manage. The addition of new agents with a positive risk–benefit ratio could potentially assist clinicians and patients in achieving adequate diabetes control. Canagliflozin, the first sodium-glucose cotransporter 2 inhibitor presently available on the market, offers a unique mechanism of action: it inhibits renal reabsorption of glucose, thereby increasing urinary glucose excretion. It reduces hemoglobin A(1c) by approximately 0.37%–1.16%; it also reduces the patient’s weight and systolic blood pressure and has a low risk for hypoglycemia. Adverse effects include an increased risk of urinary tract infections and genital mycotic infections. In this manuscript we review canagliflozin and its potential role in management of type 2 diabetes mellitus. |
format | Online Article Text |
id | pubmed-3840773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38407732013-11-27 Canagliflozin: a novel treatment option for type 2 diabetes Dietrich, Eric Powell, Jason Taylor, James R Drug Des Devel Ther Review Type 2 diabetes continues to be a challenging disease to manage. The addition of new agents with a positive risk–benefit ratio could potentially assist clinicians and patients in achieving adequate diabetes control. Canagliflozin, the first sodium-glucose cotransporter 2 inhibitor presently available on the market, offers a unique mechanism of action: it inhibits renal reabsorption of glucose, thereby increasing urinary glucose excretion. It reduces hemoglobin A(1c) by approximately 0.37%–1.16%; it also reduces the patient’s weight and systolic blood pressure and has a low risk for hypoglycemia. Adverse effects include an increased risk of urinary tract infections and genital mycotic infections. In this manuscript we review canagliflozin and its potential role in management of type 2 diabetes mellitus. Dove Medical Press 2013-11-22 /pmc/articles/PMC3840773/ /pubmed/24285921 http://dx.doi.org/10.2147/DDDT.S48937 Text en © 2013 Dietrich et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Dietrich, Eric Powell, Jason Taylor, James R Canagliflozin: a novel treatment option for type 2 diabetes |
title | Canagliflozin: a novel treatment option for type 2 diabetes |
title_full | Canagliflozin: a novel treatment option for type 2 diabetes |
title_fullStr | Canagliflozin: a novel treatment option for type 2 diabetes |
title_full_unstemmed | Canagliflozin: a novel treatment option for type 2 diabetes |
title_short | Canagliflozin: a novel treatment option for type 2 diabetes |
title_sort | canagliflozin: a novel treatment option for type 2 diabetes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840773/ https://www.ncbi.nlm.nih.gov/pubmed/24285921 http://dx.doi.org/10.2147/DDDT.S48937 |
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