Immediate Effect of Continuous Positive Airway Pressure Therapy on Sleep and Respiration in Patients with Multiple System Atrophy and Sleep-Disordered Breathing.

CPAP multiple system atrophy sleep‐disordered breathing stridor

Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
17 Sep 2024
Historique:
revised: 05 08 2024
received: 02 06 2024
accepted: 07 08 2024
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 17 9 2024
Statut: aheadofprint

Résumé

Sleep-disordered breathing (SDB; including stridor and sleep apnea syndromes) is frequent in multiple system atrophy (MSA), but the immediate effect of continuous positive airway pressure (CPAP) therapy is incompletely determined. We sought to evaluate the acute effect and safety of CPAP therapy on SDB and sleep architecture, as well as the clinical characteristics of nonresponders to CPAP therapy. The measures of 63 consecutive patients with MSA who underwent a video-polysomnography during two consecutive nights (a first night in ambient air, a second night with or without CPAP, depending on the presence of SDB and availability of CPAP) in routine care were retrospectively collected. Linear mixed models assessed the two-night change in sleep and respiratory measures, comparing those with and without the CPAP therapy on the second night. SDB was frequent and mainly associated with the cerebellar phenotype. The introduction of CPAP had immediate benefits, including the normalization of the apnea-hypopnea index and a resolution of stridor in more than two-thirds of the cases, decreased arousal index, and increased rapid eye movement sleep. CPAP therapy was well tolerated, and only two patients had emergent central apneas. Nonresponse to CPAP was generally associated with more severe motor disease. CPAP seems a well-tolerated and effective therapy in patients with MSA and SDB in the short term. This treatment shows remarkable immediate benefits by objectively improving both respiratory disturbances and sleep architecture. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND BACKGROUND
Sleep-disordered breathing (SDB; including stridor and sleep apnea syndromes) is frequent in multiple system atrophy (MSA), but the immediate effect of continuous positive airway pressure (CPAP) therapy is incompletely determined.
OBJECTIVE OBJECTIVE
We sought to evaluate the acute effect and safety of CPAP therapy on SDB and sleep architecture, as well as the clinical characteristics of nonresponders to CPAP therapy.
METHODS METHODS
The measures of 63 consecutive patients with MSA who underwent a video-polysomnography during two consecutive nights (a first night in ambient air, a second night with or without CPAP, depending on the presence of SDB and availability of CPAP) in routine care were retrospectively collected. Linear mixed models assessed the two-night change in sleep and respiratory measures, comparing those with and without the CPAP therapy on the second night.
RESULTS RESULTS
SDB was frequent and mainly associated with the cerebellar phenotype. The introduction of CPAP had immediate benefits, including the normalization of the apnea-hypopnea index and a resolution of stridor in more than two-thirds of the cases, decreased arousal index, and increased rapid eye movement sleep. CPAP therapy was well tolerated, and only two patients had emergent central apneas. Nonresponse to CPAP was generally associated with more severe motor disease.
CONCLUSIONS CONCLUSIONS
CPAP seems a well-tolerated and effective therapy in patients with MSA and SDB in the short term. This treatment shows remarkable immediate benefits by objectively improving both respiratory disturbances and sleep architecture. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 39285740
doi: 10.1002/mds.29993
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Auteurs

Giulia Lazzeri (G)

Centro Parkinson e Parkinsonismi, ASST G. Pini-CTO, Milan, Italy.
Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.

Marion Houot (M)

Center of Excellence of Neurodegenerative Disease, Pitié-Salpêtrière Hospital, AP-HP, Paris, France.
Department of Neurology, Institute of Memory and Alzheimer's Disease, Pitié-Salpêtrière Hospital, AP-HP, Paris, France.
Clinical Investigation Centre Neuroscience, Brain Institute, Pitié-Salpêtrière Hospital, Paris, France.

Maxime Patout (M)

Inserm UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Sorbonne Université, Paris, France.
Service des Pathologies du Sommeil, Pitié-Salpêtrière hospital, AP-HP, Paris, France.

Cécile Londner (C)

Service des Pathologies du Sommeil, Pitié-Salpêtrière hospital, AP-HP, Paris, France.

Carole Philippe (C)

Neurology Department, University Hospital of Limoges, Limoges, France.

Stephane Attard (S)

Service des Pathologies du Sommeil, Pitié-Salpêtrière hospital, AP-HP, Paris, France.

Teddy Delpy (T)

Service des Pathologies du Sommeil, Pitié-Salpêtrière hospital, AP-HP, Paris, France.

Joanna Ruggeri (J)

Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.
Department of Neurology, Pitié-Salpêtrière Hospital, APHP, Paris, France.

Bertrand Degos (B)

Service de Neurologie, Hôpital Avicenne, Hôpitaux Universitaires de Paris Seine-Saint-Denis, Sorbonne Paris Nord, AP-HP, Bobigny, France.
Dynamics and Pathophysiology of Neuronal Networks Team, Center for Interdisciplinary Research in Biology, Collège de France, CNRS UMR7241/INSERM U1050, Université PSL, Paris, France.

Florence Cormier (F)

Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.
Department of Neurology, Pitié-Salpêtrière Hospital, APHP, Paris, France.

Marie Vidailhet (M)

Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.
Department of Neurology, Pitié-Salpêtrière Hospital, APHP, Paris, France.

Jean Cristophe Corvol (JC)

Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.
Department of Neurology, Pitié-Salpêtrière Hospital, APHP, Paris, France.

Isabelle Arnulf (I)

Service des Pathologies du Sommeil, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.

David Grabli (D)

Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.
Department of Neurology, Pitié-Salpêtrière Hospital, APHP, Paris, France.

Pauline Dodet (P)

Service des Pathologies du Sommeil, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
Sorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.

Classifications MeSH