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Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis

Optic neuritis (ON) is an inflammatory condition involving the optic nerve. Several important typical and atypical ON variants are now recognized. Typical ON has a more favorable prognosis; it can be idiopathic or represent an early manifestation of demyelinating diseases, mostly multiple sclerosis...

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Autores principales: Saitakis, George, Chwalisz, Bart K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9456305/
https://www.ncbi.nlm.nih.gov/pubmed/36077167
http://dx.doi.org/10.3390/ijms23179769
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author Saitakis, George
Chwalisz, Bart K.
author_facet Saitakis, George
Chwalisz, Bart K.
author_sort Saitakis, George
collection PubMed
description Optic neuritis (ON) is an inflammatory condition involving the optic nerve. Several important typical and atypical ON variants are now recognized. Typical ON has a more favorable prognosis; it can be idiopathic or represent an early manifestation of demyelinating diseases, mostly multiple sclerosis (MS). The atypical spectrum includes entities such as antibody-driven ON associated with neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein antibody disease (MOGAD), chronic/relapsing inflammatory optic neuropathy (CRION), and sarcoidosis-associated ON. Appropriate and timely diagnosis is essential to rapidly decide on the appropriate treatment, maximize visual recovery, and minimize recurrences. This review paper aims at presenting the currently available state-of-the-art treatment strategies for typical and atypical ON, both in the acute phase and in the long-term. Moreover, emerging therapeutic approaches and novel steps in the direction of achieving remyelination are discussed.
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spelling pubmed-94563052022-09-09 Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis Saitakis, George Chwalisz, Bart K. Int J Mol Sci Review Optic neuritis (ON) is an inflammatory condition involving the optic nerve. Several important typical and atypical ON variants are now recognized. Typical ON has a more favorable prognosis; it can be idiopathic or represent an early manifestation of demyelinating diseases, mostly multiple sclerosis (MS). The atypical spectrum includes entities such as antibody-driven ON associated with neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein antibody disease (MOGAD), chronic/relapsing inflammatory optic neuropathy (CRION), and sarcoidosis-associated ON. Appropriate and timely diagnosis is essential to rapidly decide on the appropriate treatment, maximize visual recovery, and minimize recurrences. This review paper aims at presenting the currently available state-of-the-art treatment strategies for typical and atypical ON, both in the acute phase and in the long-term. Moreover, emerging therapeutic approaches and novel steps in the direction of achieving remyelination are discussed. MDPI 2022-08-29 /pmc/articles/PMC9456305/ /pubmed/36077167 http://dx.doi.org/10.3390/ijms23179769 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Saitakis, George
Chwalisz, Bart K.
Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis
title Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis
title_full Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis
title_fullStr Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis
title_full_unstemmed Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis
title_short Treatment and Relapse Prevention of Typical and Atypical Optic Neuritis
title_sort treatment and relapse prevention of typical and atypical optic neuritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9456305/
https://www.ncbi.nlm.nih.gov/pubmed/36077167
http://dx.doi.org/10.3390/ijms23179769
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