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Multidisciplinary Interventions in Motor Neuron Disease

Motor neuron disease is a neurodegenerative disease characterized by loss of upper motor neuron in the motor cortex and lower motor neurons in the brain stem and spinal cord. Death occurs 2–4 years after the onset of the disease. A complex interplay of cellular processes such as mitochondrial dysfun...

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Detalles Bibliográficos
Autores principales: Williams, U. E., Philip-Ephraim, E. E., Oparah, S. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437278/
https://www.ncbi.nlm.nih.gov/pubmed/26317009
http://dx.doi.org/10.1155/2014/435164
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author Williams, U. E.
Philip-Ephraim, E. E.
Oparah, S. K.
author_facet Williams, U. E.
Philip-Ephraim, E. E.
Oparah, S. K.
author_sort Williams, U. E.
collection PubMed
description Motor neuron disease is a neurodegenerative disease characterized by loss of upper motor neuron in the motor cortex and lower motor neurons in the brain stem and spinal cord. Death occurs 2–4 years after the onset of the disease. A complex interplay of cellular processes such as mitochondrial dysfunction, oxidative stress, excitotoxicity, and impaired axonal transport are proposed pathogenetic processes underlying neuronal cell loss. Currently evidence exists for the use of riluzole as a disease modifying drug; multidisciplinary team care approach to patient management; noninvasive ventilation for respiratory management; botulinum toxin B for sialorrhoea treatment; palliative care throughout the course of the disease; and Modafinil use for fatigue treatment. Further research is needed in management of dysphagia, bronchial secretion, pseudobulbar affect, spasticity, cramps, insomnia, cognitive impairment, and communication in motor neuron disease.
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spelling pubmed-44372782015-08-27 Multidisciplinary Interventions in Motor Neuron Disease Williams, U. E. Philip-Ephraim, E. E. Oparah, S. K. J Neurodegener Dis Review Article Motor neuron disease is a neurodegenerative disease characterized by loss of upper motor neuron in the motor cortex and lower motor neurons in the brain stem and spinal cord. Death occurs 2–4 years after the onset of the disease. A complex interplay of cellular processes such as mitochondrial dysfunction, oxidative stress, excitotoxicity, and impaired axonal transport are proposed pathogenetic processes underlying neuronal cell loss. Currently evidence exists for the use of riluzole as a disease modifying drug; multidisciplinary team care approach to patient management; noninvasive ventilation for respiratory management; botulinum toxin B for sialorrhoea treatment; palliative care throughout the course of the disease; and Modafinil use for fatigue treatment. Further research is needed in management of dysphagia, bronchial secretion, pseudobulbar affect, spasticity, cramps, insomnia, cognitive impairment, and communication in motor neuron disease. Hindawi Publishing Corporation 2014 2014-11-18 /pmc/articles/PMC4437278/ /pubmed/26317009 http://dx.doi.org/10.1155/2014/435164 Text en Copyright © 2014 U. E. Williams et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Williams, U. E.
Philip-Ephraim, E. E.
Oparah, S. K.
Multidisciplinary Interventions in Motor Neuron Disease
title Multidisciplinary Interventions in Motor Neuron Disease
title_full Multidisciplinary Interventions in Motor Neuron Disease
title_fullStr Multidisciplinary Interventions in Motor Neuron Disease
title_full_unstemmed Multidisciplinary Interventions in Motor Neuron Disease
title_short Multidisciplinary Interventions in Motor Neuron Disease
title_sort multidisciplinary interventions in motor neuron disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437278/
https://www.ncbi.nlm.nih.gov/pubmed/26317009
http://dx.doi.org/10.1155/2014/435164
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