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dc.contributorHospital General de Granollers
dc.contributor.authorDe Lorenzi, Andrea Beatriz
dc.contributor.authorKaplinsky, Edgardo
dc.contributor.authorRivera Zambrano, Marx
dc.contributor.authorTomás Chaume, Laia
dc.contributor.authorMonell Rosas, Joan
dc.date.accessioned2023-06-02T10:26:59Z
dc.date.available2023-06-02T10:26:59Z
dc.date.issued2023-01-04
dc.identifier.citationDe Lorenzi AB, Kaplinsky E, Zambrano MR, Chaume LT, Rosas JM. Emerging concepts in heart failure management and treatment: focus on SGLT2 inhibitors in heart failure with preserved ejection fraction. Drugs Context. 2023 Jan 4;12:2022-7-1.
dc.identifier.urihttps://hdl.handle.net/11351/9650
dc.descriptionDapagliflozin; Empagliflozin; Heart failure
dc.description.abstractThe role of sodium-glucose cotransporter 2 inhibitors (SLTG2i), developed initially as glucose-lowering agents, has represented a novelty in patients with heart failure (HF) and reduced ejection fraction (HFrEF) since dapagliflozin (DAPA-HF study) and empagliflozin (EMPEROR-Reduced study) were able to reduce morbidity and mortality in this setting regardless of the presence or absence of diabetes. In previous large clinical trials (EMPA-REG OUTCOME study, CANVAS, DECLARE-TIMI 58), SGLT2i have been shown to attenuate HF progression expressed by reducing the risk of HF hospitalizations in patients with type 2 diabetes mellitus mostly without HF at baseline. This benefit was then corroborated with positive results in HF outcomes (cardiovascular mortality and HF hospitalizations) in patients with HF with preserved ejection fraction (HFpEF) in the EMPEROR-Preserved (empagliflozin) and DELIVER (dapagliflozin) trials. Several biological mechanisms apart from the glycosuria are attributed to these agents in this last context, including anti-inflammatory effects, reduction of fibrosis and apoptosis, improvement of myocardial metabolism, mitochondrial function optimization, and oxidative stress protection. Moreover, SGLT2i can also improve ventricular loading conditions by forcing diuresis and natriuresis, and by enhancing vascular and renal function. In addition, SGLT2i can reduce myocardial passive stiffness (diastolic function) by enforcing the phosphorylation of myofilament modulatory proteins. This article provided an overview of the main pathophysiological characteristics of HFpEF and of the diverse mechanisms of action of SGLT2i in this setting. The supporting clinical evidence of SGLT2i in HFpEF (EMPEROR-Preserved and DELIVER trials) is also reviewed. This article is part of the Emerging concepts in heart failure management and treatment Special Issue: https://www.drugsincontext.com/special_issues/emerging-concepts-in-heart-failure-management-and-treatment.
dc.language.isoeng
dc.publisherBioExcel Publishing
dc.relation.ispartofseriesDrugs in Context;12
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectInsuficiència cardíaca
dc.subjectInhibidors de les glucosidases
dc.subjectCor - Malalties
dc.subject.meshHeart Failure
dc.subject.meshSodium-Glucose Transporter 2 Inhibitors
dc.subject.meshHeart Failure, Systolic
dc.titleEmerging concepts in heart failure management and treatment: focus on SGLT2 inhibitors in heart failure with preserved ejection fraction
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.7573/dic.2022-7-1
dc.subject.decsinsuficiencia cardíaca
dc.subject.decsinhibidores del cotransportador de sodio-glucosa 2
dc.subject.decsinsuficiencia cardíaca sistólica
dc.relation.publishversionhttps://doi.org/10.7573/dic.2022-7-1
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[De Lorenzi AB, Zambrano MR, Chaume LT, Rosas JM] Unitat de Cardiología, Hospital General de Granollers, Granollers, Spain. [Kaplinsky E] Cardiology Unit, Medicine Department, Hospital Municipal de Badalona, Spain
dc.identifier.pmid36660013
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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