Author:
Camilli Massimiliano,Viscovo Marcello,Maggio Luca,Bonanni Alice,Torre Ilaria,Pellegrino Claudio,Lamendola Priscilla,Tinti Lorenzo,Teofili Luciana,Hohaus Stefan,Lanza Gaetano Antonio,Ferdinandy Peter,Varga Zoltan,Crea Filippo,Lombardo Antonella,Minotti Giorgio
Abstract
AbstractSodium–glucose cotransporter 2 inhibitors (SGLT2i), a new drug class initially designed and approved for treatment of diabetes mellitus, have been shown to exert pleiotropic metabolic and direct cardioprotective and nephroprotective effects that extend beyond their glucose-lowering action. These properties prompted their use in two frequently intertwined conditions, heart failure and chronic kidney disease. Their unique mechanism of action makes SGLT2i an attractive option also to lower the rate of cardiac events and improve overall survival of oncological patients with preexisting cardiovascular risk and/or candidate to receive cardiotoxic therapies. This review will cover biological foundations and clinical evidence for SGLT2i modulating myocardial function and metabolism, with a focus on their possible use as cardioprotective agents in the cardio-oncology settings. Furthermore, we will explore recently emerged SGLT2i effects on hematopoiesis and immune system, carrying the potential of attenuating tumor growth and chemotherapy-induced cytopenias.
Funder
Università Cattolica del Sacro Cuore
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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