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Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders

Neuromyelitis optica spectrum disorders (NMOSD) are a group of autoimmune inflammatory conditions that primarily target the optic nerves, spinal cord, brainstem, and occasionally the cerebrum. NMOSD is characterized by recurrent attacks of visual, motor, and/or sensory dysfunction that often result...

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Autores principales: Abboud, Hesham, Salazar-Camelo, Andrea, George, Naveen, Planchon, Sarah M., Matiello, Marcelo, Mealy, Maureen A., Goodman, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940781/
https://www.ncbi.nlm.nih.gov/pubmed/34482456
http://dx.doi.org/10.1007/s00415-021-10783-4
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author Abboud, Hesham
Salazar-Camelo, Andrea
George, Naveen
Planchon, Sarah M.
Matiello, Marcelo
Mealy, Maureen A.
Goodman, Andrew
author_facet Abboud, Hesham
Salazar-Camelo, Andrea
George, Naveen
Planchon, Sarah M.
Matiello, Marcelo
Mealy, Maureen A.
Goodman, Andrew
author_sort Abboud, Hesham
collection PubMed
description Neuromyelitis optica spectrum disorders (NMOSD) are a group of autoimmune inflammatory conditions that primarily target the optic nerves, spinal cord, brainstem, and occasionally the cerebrum. NMOSD is characterized by recurrent attacks of visual, motor, and/or sensory dysfunction that often result in severe neurological deficits. In recent years, there has been a significant progress in relapse treatment and prevention but the residual disability per attack remains high. Although symptomatic and restorative research has been limited in NMOSD, some therapeutic approaches can be inferred from published case series and evidence from multiple sclerosis literature. In this review, we will discuss established and emerging therapeutic options for symptomatic treatment and restoration of function in NMOSD. We highlight NMOSD-specific considerations and identify potential areas for future research. The review covers pharmacologic, non-pharmacologic, and neuromodulatory approaches to neuropathic pain, tonic spasms, muscle tone abnormalities, sphincter dysfunction, motor and visual impairment, fatigue, sleep disorders, and neuropsychological symptoms. In addition, we briefly discuss remyelinating agents and mesenchymal stem cell transplantation in NMOSD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-021-10783-4.
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spelling pubmed-89407812022-04-07 Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders Abboud, Hesham Salazar-Camelo, Andrea George, Naveen Planchon, Sarah M. Matiello, Marcelo Mealy, Maureen A. Goodman, Andrew J Neurol Review Neuromyelitis optica spectrum disorders (NMOSD) are a group of autoimmune inflammatory conditions that primarily target the optic nerves, spinal cord, brainstem, and occasionally the cerebrum. NMOSD is characterized by recurrent attacks of visual, motor, and/or sensory dysfunction that often result in severe neurological deficits. In recent years, there has been a significant progress in relapse treatment and prevention but the residual disability per attack remains high. Although symptomatic and restorative research has been limited in NMOSD, some therapeutic approaches can be inferred from published case series and evidence from multiple sclerosis literature. In this review, we will discuss established and emerging therapeutic options for symptomatic treatment and restoration of function in NMOSD. We highlight NMOSD-specific considerations and identify potential areas for future research. The review covers pharmacologic, non-pharmacologic, and neuromodulatory approaches to neuropathic pain, tonic spasms, muscle tone abnormalities, sphincter dysfunction, motor and visual impairment, fatigue, sleep disorders, and neuropsychological symptoms. In addition, we briefly discuss remyelinating agents and mesenchymal stem cell transplantation in NMOSD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-021-10783-4. Springer Berlin Heidelberg 2021-09-05 2022 /pmc/articles/PMC8940781/ /pubmed/34482456 http://dx.doi.org/10.1007/s00415-021-10783-4 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Abboud, Hesham
Salazar-Camelo, Andrea
George, Naveen
Planchon, Sarah M.
Matiello, Marcelo
Mealy, Maureen A.
Goodman, Andrew
Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
title Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
title_full Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
title_fullStr Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
title_full_unstemmed Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
title_short Symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
title_sort symptomatic and restorative therapies in neuromyelitis optica spectrum disorders
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940781/
https://www.ncbi.nlm.nih.gov/pubmed/34482456
http://dx.doi.org/10.1007/s00415-021-10783-4
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