Vocal cord electromyographic correlates of stridor in multiple system atrophy phenotypes.


Journal

Parkinsonism & related disorders
ISSN: 1873-5126
Titre abrégé: Parkinsonism Relat Disord
Pays: England
ID NLM: 9513583

Informations de publication

Date de publication:
01 2020
Historique:
received: 19 08 2019
revised: 20 11 2019
accepted: 26 11 2019
pubmed: 7 12 2019
medline: 18 12 2020
entrez: 7 12 2019
Statut: ppublish

Résumé

Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by dysautonomia in combination with parkinsonian and cerebellar signs. Stridor may also occur and it is associated with life-threatening events and poor prognosis. The pathophysiology of stridor in MSA is still debated. To define correlations between diurnal electromyographic (EMG) abnormalities of vocal cord muscles and stridor in MSA phenotypes. We recruited 60 patients with "probable" MSA (45 with parkinsonian [MSA-P] and 15 with cerebellar phenotype [MSA-C]). Nocturnal stridor was detected with video-polysomnography, whereas diurnal stridor was clinically noted when present. A diurnal kinesiologic EMG study of the adductor thyroarytenoid and the abductor posterior cricoarytenoid muscles was also performed. Among subjects with nocturnal stridor, MSA-P patients predominantly showed a paradoxical burst-like activation of the adductor thyroarytenoid muscle during inspiration. This dystonic pattern was associated with nocturnal stridor in MSA-P (odds ratio [OR] = 23.64, 95% confidence interval [CI] 3.42-70.77, p < 0.001). Conversely, MSA-C patients with nocturnal stridor mainly had additional neurogenic findings of vocal cord muscles. This dystonic-plus pattern correlated with nocturnal stridor in MSA-C (OR = 17.21, 95% CI 4.17-74.92, p < 0.01). The findings of diurnal stridor paralleled the observations for nocturnal stridor. The pathophysiology of stridor may differ between MSA phenotypes, possibly related to dysfunctional supranuclear mechanisms in MSA-P (dystonic pattern) and to additional nuclear damage in MSA-C (dystonic-plus pattern).

Identifiants

pubmed: 31809947
pii: S1353-8020(19)30519-X
doi: 10.1016/j.parkreldis.2019.11.025
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

31-35

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Massimiliano Todisco (M)

Parkinson's Disease and Movement Disorders Unit, IRCCS Mondino Foundation, Pavia, Italy; Department of Neurophysiopathology, IRCCS Mondino Foundation, Pavia, Italy.

Enrico Alfonsi (E)

Department of Neurophysiopathology, IRCCS Mondino Foundation, Pavia, Italy. Electronic address: enrico.alfonsi@mondino.it.

Ioannis Ugo Isaias (IU)

Department of Neurology, University Hospital Würzburg and Julius Maximilian University of Würzburg, Würzburg, Germany.

Roberta Zangaglia (R)

Parkinson's Disease and Movement Disorders Unit, IRCCS Mondino Foundation, Pavia, Italy.

Brigida Minafra (B)

Parkinson's Disease and Movement Disorders Unit, IRCCS Mondino Foundation, Pavia, Italy.

Giuseppe Cosentino (G)

Department of Neurophysiopathology, IRCCS Mondino Foundation, Pavia, Italy.

Michele Terzaghi (M)

Sleep Medicine and Epilepsy Unit, IRCCS Mondino Foundation, Pavia, Italy.

Nicoló Gabriele Pozzi (NG)

Parkinson's Disease and Movement Disorders Unit, IRCCS Mondino Foundation, Pavia, Italy; Department of Neurology, University Hospital Würzburg and Julius Maximilian University of Würzburg, Würzburg, Germany.

Raffaele Manni (R)

Sleep Medicine and Epilepsy Unit, IRCCS Mondino Foundation, Pavia, Italy.

Claudio Pacchetti (C)

Parkinson's Disease and Movement Disorders Unit, IRCCS Mondino Foundation, Pavia, Italy.

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Classifications MeSH