Angiotensin receptor/Neprilysin inhibitor effects in CRTd non-responders: From epigenetic to clinical beside

We evaluated whether Angiotensin receptor/Neprilysin inhibitors (ARNI) reduce heart failure (HF) hospitalizations and deaths in cardiac resynchronization therapy with defibrillator (CRTd) non-responders patients at 12 months of follow-up, modulating microRNAs (miRs) implied in adverse cardiac remode...

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Veröffentlicht in:Pharmacological research 2022-08, Vol.182, p.106303-106303, Article 106303
Hauptverfasser: Sardu, Celestino, Massetti, Massimo, Scisciola, Lucia, Trotta, Maria Consiglia, Santamaria, Matteo, Volpicelli, Mario, Ducceschi, Valentino, Signoriello, Giuseppe, D’Onofrio, Nunzia, Marfella, Ludovica, Casolaro, Flavia, Amico, Michele D.’, Ruocco, Antonio, Balestrieri, Maria Luisa, Mauro, Ciro, Rafaniello, Concetta, Capuano, Annalisa, Paolisso, Giuseppe, Marfella, Raffaele
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Sprache:eng
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Zusammenfassung:We evaluated whether Angiotensin receptor/Neprilysin inhibitors (ARNI) reduce heart failure (HF) hospitalizations and deaths in cardiac resynchronization therapy with defibrillator (CRTd) non-responders patients at 12 months of follow-up, modulating microRNAs (miRs) implied in adverse cardiac remodeling. adverse cardiac remodeling characterized by left ventricle ejection fraction (LVEF) reduction, left ventricular end-systolic volume (LVESv) increase, and the 6-minute walking test (6MWT) reduction are relevant pathological mechanisms in CRTd non-responders and could be linked to changes in miRNAs (miRs), regulating cardiac fibrosis, apoptosis, and hypertrophy. miRs levels and clinical outcomes (LVEF, cardiac deaths, and 6MWT) were evaluated at baseline and one year of follow-up in CRTd non-responders divided into ARNI-users and Non-ARNI users. At baseline, there were no differences in levels of inflammatory markers, miR-18, miR-145, and miR-181 (p > 0.05) between Non-ARNI users (n 106) and ARNI-users (n 312). At one year of follow-up, ARNI-users vs. Non-ARNI users showed lowest inflammatory markers (p 
ISSN:1043-6618
1096-1186
DOI:10.1016/j.phrs.2022.106303