| Literature DB >> 35726047 |
Michele Correale1, Pietro Mazzeo2, Lucia Tricarico2, Francesca Croella2, Martino Fortunato2, Michele Magnesa2, Marco Amatruda2, Simona Alfieri2, Salvatore Ferrara2, Vincenzo Ceci2, Giuseppe Dattilo3, Marco Mele4, Massimo Iacoviello2, Natale Daniele Brunetti2.
Abstract
Cardiac remodelling is an adverse phenomenon linked to heart failure progression and an important contributor to heart failure severity. Cardiac remodelling could represent the real therapeutic goal in the treatment of patients with heart failure with reduced ejection fraction, being potentially reversed through different pharmacotherapies. Currently, there are well-established drugs such as angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers and β-blockers with anti-remodelling effects; recently, angiotensin receptor neprilysin inhibitor effects on inhibiting cardiac remodelling (improving N-terminal pro-B-type natriuretic peptide levels, echocardiographic parameters of reverse cardiac remodelling and right ventricular function in patients with heart failure with reduced ejection fraction) were demonstrated. More recently, hemodynamic consequences of gliflozins, reduced cardiac hydrostatic pressure as a possible cause of ventricular remodelling and hypertrophy were proposed to explain potential anti-remodelling effects of gliflozins. Gliflozins exert their cardioprotective effects by attenuating myofibroblast activity and collagen-mediated remodelling. Another postulated mechanism is represented by the reduction in sympathetic activity, through the reduction in renal afferent nervous activity and the suppression of central reflex mechanisms. Benefits of gliflozins on left ventricular hypertrophy, dilation, and systolic and diastolic function were also described. In this review, we aimed to provide a wide overview on cardiac remodelling with a particular focus on possible anti-remodelling effects of angiotensin receptor neprilysin inhibitors and gliflozins.Entities:
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Year: 2022 PMID: 35726047 DOI: 10.1007/s40261-022-01166-2
Source DB: PubMed Journal: Clin Drug Investig ISSN: 1173-2563 Impact factor: 2.859