Literature DB >> 33338309

Dysphagia in neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein antibody disease as a surrogate of brain involvement?

Marc Pawlitzki1, Sigrid Ahring1, Leoni Rolfes1, Rainer Dziewas1, Tobias Warnecke1, Sonja Suntrup-Krueger1,2, Heinz Wiendl1, Luisa Klotz1, Sven G Meuth1, Bendix Labeit1,2.   

Abstract

BACKGROUND AND
PURPOSE: Neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein antibody disease (MOGAD) are demyelinating disorders that typically affect the optic nerves and the spinal cord. However, recent studies have demonstrated various forms of brain involvement indicating encephalitic syndromes, which consequently are included in the diagnostic criteria for both. Swallowing is processed in a distributed brain network and is therefore disturbed in many neurological diseases. The aim of this study was to investigate the occurrence of oropharyngeal dysphagia in NMOSD and MOGAD using flexible endoscopic evaluation of swallowing (FEES) as a surrogate parameter of brain involvement.
METHODS: Thirteen patients with NMOSD and MOGAD (mean age 54.2 ± 18.6 years, six men) who received FEES during clinical routine were retrospectively reviewed. Their extent of oropharyngeal dysphagia was rated using an ordinal dysphagia severity scale. FEES results were compared to a control group of healthy individuals. Dysphagia severity was correlated with the presence of clinical and radiological signs of brain involvement, the Expanded Disability Status Scale (EDSS) and the occurrence of pneumonia.
RESULTS: Oropharyngeal dysphagia was present in 8/13 patients, including six patients without other clinical indication of brain involvement. Clinical or subclinical swallowing impairment was significantly more severe in patients with NMOSD and MOGAD compared to the healthy individuals (p = 0.009) and correlated with clinical signs of brain involvement (p = 0.038), higher EDSS (p = 0.006) and pneumonia (p = 0.038).
CONCLUSION: Oropharyngeal dysphagia can occur in NMOSD and MOGAD and might be associated with pneumonia and disability. FEES may help to detect subclinical brain involvement.
© 2020 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of NeurologyEuropean Academy of Neurology.

Entities:  

Keywords:  aquaporin-4 antibody; dysphagia; flexible endoscopic evaluation of swallowing; myelin oligodendrocyte glycoprotein antibody disease; neuromyelitis optica spectrum disorder

Year:  2021        PMID: 33338309     DOI: 10.1111/ene.14691

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  3 in total

1.  Successful treatment of intubation-induced severe neurogenic post-extubation dysphagia using pharyngeal electrical stimulation in a COVID-19 survivor: a case report.

Authors:  Marianna Traugott; Wolfgang Hoepler; Reinhard Kitzberger; Sophie Pavlata; Tamara Seitz; Sebastian Baumgartner; Gudrun Placher-Sorko; Daniela Pirker-Krassnig; Urs Ehehalt; Andreas Grasnek; Michaela Beham-Kacerovsky; Emanuela Friese; Christoph Wenisch; Stephanie Neuhold
Journal:  J Med Case Rep       Date:  2021-03-22

2.  Botulinum toxin injection combined with traditional swallowing rehabilitation improved cricopharyngeal dysfunction in neuromyelitis optica spectrum disorder: A case report.

Authors:  Zitong He; Fei Zhao; Yilong Shan; Zulin Dou; Hongmei Wen
Journal:  Front Neurol       Date:  2022-07-28       Impact factor: 4.086

Review 3.  Autoimmune Neurogenic Dysphagia.

Authors:  Panos Stathopoulos; Marinos C Dalakas
Journal:  Dysphagia       Date:  2021-07-05       Impact factor: 2.733

  3 in total

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