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Emerging concepts in heart failure management and treatment: focus on SGLT2 inhibitors in heart failure with preserved ejection fraction.
De Lorenzi, Andrea Beatriz; Kaplinsky, Edgardo; Zambrano, Marx Rivera; Chaume, Laia Tomás; Rosas, Joan Monell.
Afiliação
  • De Lorenzi AB; Unitat de Cardiología, Hospital General de Granollers, Barcelona, Spain.
  • Kaplinsky E; Cardiology Unit, Medicine Department, Hospital Municipal de Badalona, Spain.
  • Zambrano MR; Unitat de Cardiología, Hospital General de Granollers, Barcelona, Spain.
  • Chaume LT; Unitat de Cardiología, Hospital General de Granollers, Barcelona, Spain.
  • Rosas JM; Unitat de Cardiología, Hospital General de Granollers, Barcelona, Spain.
Drugs Context ; 122023.
Article em En | MEDLINE | ID: mdl-36660013
ABSTRACT
The 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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article