Impact of angiotensin receptor-neprilysin inhibition on vascular function in heart failure with reduced ejection fraction: A pilot study.


Journal

Physiological reports
ISSN: 2051-817X
Titre abrégé: Physiol Rep
Pays: United States
ID NLM: 101607800

Informations de publication

Date de publication:
03 2022
Historique:
received: 24 01 2022
accepted: 30 01 2022
entrez: 5 3 2022
pubmed: 6 3 2022
medline: 14 4 2022
Statut: ppublish

Résumé

The mechanisms for the benefits of Angiotensin Receptor Neprilysin Inhibition (ARNi) in heart failure patients with reduced ejection fraction (HFrEF) are likely beyond blood pressure reduction. Measures of vascular function such as arterial stiffness and endothelial function are strong prognostic markers of cardiovascular outcomes in HFrEF, yet the impact of ARNi on vascular health remains to be explored. We hypothesized that arterial stiffness and endothelial function would improve after 12 weeks of ARNi in HFrEF. We tested 10 stable HFrEF patients at baseline and following 12 weeks of ARNi [64 ± 9 years, Men/Women: 9/1, left ventricular ejection fraction (EF): 28 ± 6%] as well as 10 stable HFrEF patients that remained on conventional treatment (CON: 60 ± 7 years, Men/Women: 6/4, EF: 31 ± 5%; all p = NS). Arterial stiffness was assessed via carotid-femoral pulse wave velocity (PWV) and endothelial function was assessed via brachial artery flow-mediated dilation (FMD). PWV decreased after 12 weeks of ARNi (9.0 ± 2.1 vs. 7.1 ± 1.2 m/s; p < 0.01) but not in CON (7.0 ± 2.4 vs. 7.5 ± 2.3 m/s; p = 0.35), an effect that remained when controlling for reductions in mean arterial pressure (p < 0.01). FMD increased after 12 weeks of ARNi (2.2 ± 1.9 vs. 5.5 ± 2.1%; p < 0.001) but not in CON (4.8 ± 3.8 vs. 5.4 ± 3.4%; p = 0.34). Baseline PWV (p = 0.06) and FMD (p = 0.07) were not different between groups. These preliminary data suggest that 12 weeks of ARNi therapy may reduce arterial stiffness and improve endothelial function in HFrEF. Thus, the findings from this pilot study suggest that the benefits of ARNi are beyond blood pressure reduction and include improvements in vascular function.

Identifiants

pubmed: 35246960
doi: 10.14814/phy2.15209
pmc: PMC8897740
doi:

Substances chimiques

Aminobutyrates 0
Angiotensins 0
Receptors, Angiotensin 0
Neprilysin EC 3.4.24.11

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e15209

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM113125
Pays : United States

Informations de copyright

© 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.

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Auteurs

Sangeetha Nathaniel (S)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

Shane McGinty (S)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

Melissa A H Witman (MAH)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

David G Edwards (DG)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

William B Farquhar (WB)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

Vinay Hosmane (V)

Hosmane Cardiology and Section of Cardiology, Christiana Care Healthcare System, Newark, Delaware, USA.

Megan M Wenner (MM)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

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Classifications MeSH