Practical approach to initiating SGLT2 inhibitors in type 2 diabetes

Author

Gomez-Peralta, Fernando

Abreu, Cristina

Lecube Torelló, Albert

Bellido, Diego

Soto, Alfonso

Morales, Cristóbal

Brito-Sanfiel, Miguel

Umpierrez, Guillermo

Publication date

2017-11-20T11:01:19Z

2017-11-20T11:01:19Z

2017



Abstract

Sodium-glucose co-transporter 2 (SGLT2) inhibitors are an attractive novel therapeutic option for the treatment of type 2 diabetes. They block the reabsorption of filtered glucose in kidneys, mainly in proximal renal tubules, resulting in increased urinary glucose excretion and correction of the diabetes-related hyperglycemia. Beyond improving glucose control, SGLT2 inhibitors offer potential benefits by reducing body weight and blood pressure. On the basis of the efficacy demonstrated in clinical trials, SGLT2 inhibitors are recommended as second- or third-line agents for the management of patients with type 2 diabetes. Beneficial effects on kidney disease progression, cardiovascular and all-cause mortality, and hospitalization for heart failure have also been demonstrated with one SGLT2 inhibitor (empagliflozin). Potential adverse events resulting from their mechanism of action or related to concomitant therapies are reviewed. A treatment algorithm for the adjustment of concomitant therapies after initiating SGLT2 inhibitors is also proposed.


Astra-Zeneca España contributed to support medical writing activities provided by Meysis S.L. No other external funding was received for this manuscript, which was written thanks to the unconditional effort of all authors.

Document Type

article
publishedVersion

Language

English

Subjects and keywords

Concomitant; Initiation; Management; SGLT2 inhibitors

Publisher

Springer Verlag

Related items

Reproducció del document publicat a https://doi.org/10.1007/s13300-017-0277-0

Diabetes Therapy, 2017, vol. 8, núm. 5, p. 953-962

Rights

cc-by-nc (c) Gomez-Peralta et al., 2017

http://creativecommons.org/licenses/by-nc/4.0/

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