Sleep Outcomes From AWAKE-HF: A Randomized Clinical Trial of Sacubitril/Valsartan vs Enalapril in Patients With Heart Failure and Reduced Ejection Fraction.


Journal

Journal of cardiac failure
ISSN: 1532-8414
Titre abrégé: J Card Fail
Pays: United States
ID NLM: 9442138

Informations de publication

Date de publication:
12 2021
Historique:
received: 03 03 2021
revised: 28 07 2021
accepted: 28 07 2021
pubmed: 25 8 2021
medline: 29 12 2021
entrez: 24 8 2021
Statut: ppublish

Résumé

Heart failure and sleep-disordered breathing have been increasingly recognized as co-occurring conditions. Their bidirectional relationship warrants investigation into whether heart failure therapy improves sleep and sleep-disordered breathing. We sought to explore the effect of treatment with sacubitril/valsartan on sleep-related endpoints from the AWAKE-HF study. AWAKE-HF was a randomized, double-blind study conducted in 23 centers in the United States. Study participants with heart failure with reduced rejection fraction and New York Heart Association class II or III symptoms were randomly assigned to receive treatment with either sacubitril/valsartan or enalapril. All endpoints were assessed at baseline and after 8 weeks of treatment. Portable sleep-monitoring equipment was used to measure the apnea-hypopnea index, including obstructive and central events. Total sleep time, wake after sleep onset and sleep efficiency were exploratory measures assessed using wrist actigraphy. 140 patients received treatment in the double-blind phase (sacubitril/valsartan, n = 70; enalapril, n = 70). At baseline, 39% and 40% of patients randomly assigned to receive sacubitril/valsartan or enalapril, respectively, presented with undiagnosed, untreated, moderate-to-severe sleep-disordered breathing (≥ 15 events/h), and nearly all had obstructive sleep apnea. After 8 weeks of treatment, the mean 4% apnea-hypopnea index changed minimally from 16.3/h to 15.2/h in the sacubitril/valsartan group and from 16.8/h to 17.6/h in the enalapril group. Mean total sleep time was long at baseline and decreased only slightly in both treatment groups at week 8 (-14 and -11 minutes for sacubitril/valsartan and enalapril, respectively), with small changes in wake after sleep onset and sleep efficiency in both groups. In a cohort of patients with heart failure with reduced rejection fraction who met prescribing guidelines for sacubitril/valsartan, one-third had undiagnosed moderate-to-severe obstructive sleep apnea. The addition of sacubitril/valsartan therapy did not significantly improve sleep-disordered breathing or sleep duration or efficiency. Patients who meet indications for treatment with sacubitril/valsartan should be evaluated for sleep-disordered breathing.

Sections du résumé

BACKGROUND
Heart failure and sleep-disordered breathing have been increasingly recognized as co-occurring conditions. Their bidirectional relationship warrants investigation into whether heart failure therapy improves sleep and sleep-disordered breathing. We sought to explore the effect of treatment with sacubitril/valsartan on sleep-related endpoints from the AWAKE-HF study.
METHODS AND RESULTS
AWAKE-HF was a randomized, double-blind study conducted in 23 centers in the United States. Study participants with heart failure with reduced rejection fraction and New York Heart Association class II or III symptoms were randomly assigned to receive treatment with either sacubitril/valsartan or enalapril. All endpoints were assessed at baseline and after 8 weeks of treatment. Portable sleep-monitoring equipment was used to measure the apnea-hypopnea index, including obstructive and central events. Total sleep time, wake after sleep onset and sleep efficiency were exploratory measures assessed using wrist actigraphy.
THE RESULTS WERE AS FOLLOWS
140 patients received treatment in the double-blind phase (sacubitril/valsartan, n = 70; enalapril, n = 70). At baseline, 39% and 40% of patients randomly assigned to receive sacubitril/valsartan or enalapril, respectively, presented with undiagnosed, untreated, moderate-to-severe sleep-disordered breathing (≥ 15 events/h), and nearly all had obstructive sleep apnea. After 8 weeks of treatment, the mean 4% apnea-hypopnea index changed minimally from 16.3/h to 15.2/h in the sacubitril/valsartan group and from 16.8/h to 17.6/h in the enalapril group. Mean total sleep time was long at baseline and decreased only slightly in both treatment groups at week 8 (-14 and -11 minutes for sacubitril/valsartan and enalapril, respectively), with small changes in wake after sleep onset and sleep efficiency in both groups.
CONCLUSIONS
In a cohort of patients with heart failure with reduced rejection fraction who met prescribing guidelines for sacubitril/valsartan, one-third had undiagnosed moderate-to-severe obstructive sleep apnea. The addition of sacubitril/valsartan therapy did not significantly improve sleep-disordered breathing or sleep duration or efficiency. Patients who meet indications for treatment with sacubitril/valsartan should be evaluated for sleep-disordered breathing.

Identifiants

pubmed: 34428592
pii: S1071-9164(21)00340-7
doi: 10.1016/j.cardfail.2021.07.021
pii:
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Tetrazoles 0
sacubitril 17ERJ0MKGI
Enalapril 69PN84IO1A
Valsartan 80M03YXJ7I

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1466-1471

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Robert L Owens (RL)

From the Division of Pulmonary, Critical Care, and Sleep Medicine, San Diego School of Medicine, University of California, La Jolla, CA. Electronic address: rowens@health.ucsd.edu.

Kade Birkeland (K)

Clinical Transformation, Cedars-Sinai Health System, Beverly Hills, CA.

J Thomas Heywood (JT)

Division of Cardiovascular Medicine, Scripps Clinic, San Diego, CA.

Steven R Steinhubl (SR)

Digital Medicine, Scripps Research Translational Science Institute, San Diego, CA.

Jonas Dorn (J)

Novartis Pharma AG, Basel, Switzerland.

Daniel Grant (D)

Novartis Gene Therapy, Bannockburn, IL.

Emmanuel Fombu (E)

Locust Walk Partners Biopharma, Boston, MA (former employee of US Clinical Development and Medical Affairs, Novartis Pharmaceuticals, East Hanover, NJ).

Raj Khandwalla (R)

Department of Cardiology, Cedars-Sinai Care Foundation, Smidt Heart Institute, Beverly Hills, CA.

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Classifications MeSH