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An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes
Caring for patients with type 2 diabetes mellitus (T2DM) has entered an era with many recent additions to the regimens used to clinically control their hyperglycemia. The most recent class of agents approved by the Food and Drug Administration (FDA) for T2DM is the sodium–glucose-linked transporter...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322811/ https://www.ncbi.nlm.nih.gov/pubmed/28255241 http://dx.doi.org/10.2147/VHRM.S105721 |
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author | Messana, Joseph A Schwartz, Stanley S Townsend, Raymond R |
author_facet | Messana, Joseph A Schwartz, Stanley S Townsend, Raymond R |
author_sort | Messana, Joseph A |
collection | PubMed |
description | Caring for patients with type 2 diabetes mellitus (T2DM) has entered an era with many recent additions to the regimens used to clinically control their hyperglycemia. The most recent class of agents approved by the Food and Drug Administration (FDA) for T2DM is the sodium–glucose-linked transporter type 2 (SGLT2) inhibitors, which work principally in the proximal tubule of the kidney to block filtered glucose reabsorption. In the few years attending this new class arrival in the market, there has been a great deal of interest generated by the novel mechanism of action of SGLT2 inhibitors and by recent large outcome trials suggesting benefit on important clinical outcomes such as death, cardiovascular disease and kidney disease progression. In this review, we focus on canagliflozin, the first-in-class marketed SGLT2 inhibitor in the USA. In some cases, we included data from other SGLT2 inhibitors, such as outcomes in clinical trials, important insights on clinical features and benefits, and adverse effects. These agents represent a fundamentally different way of controlling blood glucose and for the first time in T2DM care to offer the opportunity to reduce glucose, blood pressure, and weight with effects sustained for at least 2 years. Important side effects include genital mycotic infections and the potential for orthostatic hypotension and rare instances of normoglycemic ketoacidosis. Active ongoing clinical trials promise to deepen our experience with the potential benefits, as well as the clinical risks attending the use of this new group of antidiabetic agents. |
format | Online Article Text |
id | pubmed-5322811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53228112017-03-02 An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes Messana, Joseph A Schwartz, Stanley S Townsend, Raymond R Vasc Health Risk Manag Review Caring for patients with type 2 diabetes mellitus (T2DM) has entered an era with many recent additions to the regimens used to clinically control their hyperglycemia. The most recent class of agents approved by the Food and Drug Administration (FDA) for T2DM is the sodium–glucose-linked transporter type 2 (SGLT2) inhibitors, which work principally in the proximal tubule of the kidney to block filtered glucose reabsorption. In the few years attending this new class arrival in the market, there has been a great deal of interest generated by the novel mechanism of action of SGLT2 inhibitors and by recent large outcome trials suggesting benefit on important clinical outcomes such as death, cardiovascular disease and kidney disease progression. In this review, we focus on canagliflozin, the first-in-class marketed SGLT2 inhibitor in the USA. In some cases, we included data from other SGLT2 inhibitors, such as outcomes in clinical trials, important insights on clinical features and benefits, and adverse effects. These agents represent a fundamentally different way of controlling blood glucose and for the first time in T2DM care to offer the opportunity to reduce glucose, blood pressure, and weight with effects sustained for at least 2 years. Important side effects include genital mycotic infections and the potential for orthostatic hypotension and rare instances of normoglycemic ketoacidosis. Active ongoing clinical trials promise to deepen our experience with the potential benefits, as well as the clinical risks attending the use of this new group of antidiabetic agents. Dove Medical Press 2017-02-17 /pmc/articles/PMC5322811/ /pubmed/28255241 http://dx.doi.org/10.2147/VHRM.S105721 Text en © 2017 Messana et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. 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 Messana, Joseph A Schwartz, Stanley S Townsend, Raymond R An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
title | An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
title_full | An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
title_fullStr | An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
title_full_unstemmed | An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
title_short | An evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
title_sort | evidence-based practice-oriented review focusing on canagliflozin in the management of type 2 diabetes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322811/ https://www.ncbi.nlm.nih.gov/pubmed/28255241 http://dx.doi.org/10.2147/VHRM.S105721 |
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