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Sodium-glucose co-transporter 2 inhibitors beyond diabetes

Sodium-glucose co-transporter 2 (SGLT2) inhibitors lower blood glucose by reducing the reabsorption of glucose in the kidney. They are a second-line therapy for type 2 diabetes. During clinical trials it was noticed that SGLT2 inhibitors had favourable effects on cardiovascular and renal disease. Th...

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Autores principales: Williams, Dimity L, Rofail, Serena, Atherton, John J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: NPS MedicineWise 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427625/
https://www.ncbi.nlm.nih.gov/pubmed/36110166
http://dx.doi.org/10.18773/austprescr.2022.036
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author Williams, Dimity L
Rofail, Serena
Atherton, John J
author_facet Williams, Dimity L
Rofail, Serena
Atherton, John J
author_sort Williams, Dimity L
collection PubMed
description Sodium-glucose co-transporter 2 (SGLT2) inhibitors lower blood glucose by reducing the reabsorption of glucose in the kidney. They are a second-line therapy for type 2 diabetes. During clinical trials it was noticed that SGLT2 inhibitors had favourable effects on cardiovascular and renal disease. This led to further trials that included patients without diabetes. In studies of heart failure, SGLT2 inhibitors were beneficial in treating patients with a reduced left ventricular ejection fraction. A recent study has also reported benefits in patients with a preserved ejection fraction. In chronic kidney disease, SGLT2 inhibitors may reduce disease progression. However, a decline in the glomerular filtration rate may be seen at the start of treatment. As most experience with SGLT2 inhibitors is in diabetes, patients without diabetes need to be aware of why they are being prescribed these drugs. Some of the potential indications for SGLT2 inhibitors beyond diabetes are not yet approved by regulatory authorities.
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spelling pubmed-94276252022-09-14 Sodium-glucose co-transporter 2 inhibitors beyond diabetes Williams, Dimity L Rofail, Serena Atherton, John J Aust Prescr Article Sodium-glucose co-transporter 2 (SGLT2) inhibitors lower blood glucose by reducing the reabsorption of glucose in the kidney. They are a second-line therapy for type 2 diabetes. During clinical trials it was noticed that SGLT2 inhibitors had favourable effects on cardiovascular and renal disease. This led to further trials that included patients without diabetes. In studies of heart failure, SGLT2 inhibitors were beneficial in treating patients with a reduced left ventricular ejection fraction. A recent study has also reported benefits in patients with a preserved ejection fraction. In chronic kidney disease, SGLT2 inhibitors may reduce disease progression. However, a decline in the glomerular filtration rate may be seen at the start of treatment. As most experience with SGLT2 inhibitors is in diabetes, patients without diabetes need to be aware of why they are being prescribed these drugs. Some of the potential indications for SGLT2 inhibitors beyond diabetes are not yet approved by regulatory authorities. NPS MedicineWise 2022-08-01 2022-08 /pmc/articles/PMC9427625/ /pubmed/36110166 http://dx.doi.org/10.18773/austprescr.2022.036 Text en (c) NPS MedicineWIse https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND) 4.0 License.
spellingShingle Article
Williams, Dimity L
Rofail, Serena
Atherton, John J
Sodium-glucose co-transporter 2 inhibitors beyond diabetes
title Sodium-glucose co-transporter 2 inhibitors beyond diabetes
title_full Sodium-glucose co-transporter 2 inhibitors beyond diabetes
title_fullStr Sodium-glucose co-transporter 2 inhibitors beyond diabetes
title_full_unstemmed Sodium-glucose co-transporter 2 inhibitors beyond diabetes
title_short Sodium-glucose co-transporter 2 inhibitors beyond diabetes
title_sort sodium-glucose co-transporter 2 inhibitors beyond diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427625/
https://www.ncbi.nlm.nih.gov/pubmed/36110166
http://dx.doi.org/10.18773/austprescr.2022.036
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