Angiotensin Receptor-Neprilysin Inhibitor Is Associated With Improved Cardiac Autonomic Function in Heart Failure.

ARNI cardiac autonomic nervous system heart failure heart rate variability parasympathetic

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
31 Jul 2024
Historique:
medline: 31 7 2024
pubmed: 31 7 2024
entrez: 31 7 2024
Statut: aheadofprint

Résumé

Heart failure with reduced ejection fraction is associated with potentially deleterious imbalance of the cardiac autonomic nervous system. Sacubitril/valsartan (angiotensin receptor-neprilysin inhibitor [ARNI]) reduces cardiovascular mortality and hospitalization for heart failure with reduced ejection fraction. Whether ARNI affects the cardiac autonomic nervous system has not been studied. This investigator-initiated, prospective, single-center cohort study compared heart rate (HR) variability, HR, deceleration capacity, and periodic repolarization dynamics as noninvasive measures of the cardiac autonomic nervous system before and after initiation of ARNI therapy. Patients underwent standardized 12-lead Holter-ECG, echocardiography and laboratory testing before and 3 months after start of therapy. End points were changes in HR variability (SD of normal-to-normal intervals, mean square of differences between consecutive R-R intervals), HR, deceleration capacity, and periodic repolarization dynamics as well as ventricular function and NT-proBNP (N-terminal pro-B-type natriuretic peptide). Of 63 patients with heart failure with reduced ejection fraction enrolled, 48 (76.2%) patients were still on ARNI at follow-up. SD of normal-to-normal intervals increased from 25 to 36 milliseconds ( Three months of ARNI therapy resulted in a significant increase in cardiac parasympathetic tone. The improvement in autonomic properties may be mediated by "volume unloading" and likely contributes to the beneficial effects of ARNI in heart failure with reduced ejection fraction. URL: https://www.clinicaltrials.gov; Unique Identifier: NCT04587947.

Sections du résumé

BACKGROUND BACKGROUND
Heart failure with reduced ejection fraction is associated with potentially deleterious imbalance of the cardiac autonomic nervous system. Sacubitril/valsartan (angiotensin receptor-neprilysin inhibitor [ARNI]) reduces cardiovascular mortality and hospitalization for heart failure with reduced ejection fraction. Whether ARNI affects the cardiac autonomic nervous system has not been studied.
METHODS AND RESULTS RESULTS
This investigator-initiated, prospective, single-center cohort study compared heart rate (HR) variability, HR, deceleration capacity, and periodic repolarization dynamics as noninvasive measures of the cardiac autonomic nervous system before and after initiation of ARNI therapy. Patients underwent standardized 12-lead Holter-ECG, echocardiography and laboratory testing before and 3 months after start of therapy. End points were changes in HR variability (SD of normal-to-normal intervals, mean square of differences between consecutive R-R intervals), HR, deceleration capacity, and periodic repolarization dynamics as well as ventricular function and NT-proBNP (N-terminal pro-B-type natriuretic peptide). Of 63 patients with heart failure with reduced ejection fraction enrolled, 48 (76.2%) patients were still on ARNI at follow-up. SD of normal-to-normal intervals increased from 25 to 36 milliseconds (
CONCLUSIONS CONCLUSIONS
Three months of ARNI therapy resulted in a significant increase in cardiac parasympathetic tone. The improvement in autonomic properties may be mediated by "volume unloading" and likely contributes to the beneficial effects of ARNI in heart failure with reduced ejection fraction.
REGISTRATION BACKGROUND
URL: https://www.clinicaltrials.gov; Unique Identifier: NCT04587947.

Identifiants

pubmed: 39082399
doi: 10.1161/JAHA.123.033538
doi:

Banques de données

ClinicalTrials.gov
['NCT04587947']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e033538

Auteurs

Andreas A Boehmer (AA)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Tim Schubert (T)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Moritz Rothe (M)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Christoph Keim (C)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Lilli Wiedenmann (L)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Christian Ruckes (C)

University Medical Center Mainz Interdisciplinary Center for Clinical Trials Mainz Germany.

Lukas von Stuelpnagel (L)

Division of Cardiology LMU University Hospital Munich Munich Germany.

Fabian Theurl (F)

Division of Cardiology Medical University of Innsbruck Innsbruck Austria.

Michael Schreinlechner (M)

Division of Cardiology Medical University of Innsbruck Innsbruck Austria.

Bianca C Dobre (BC)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Bernhard M Kaess (BM)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Axel Bauer (A)

Division of Cardiology Medical University of Innsbruck Innsbruck Austria.

Joachim R Ehrlich (JR)

Division of Cardiology St. Josefs-Hospital Wiesbaden Wiesbaden Germany.

Classifications MeSH