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Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis

BACKGROUND AND AIMS: Various attempts have been made to support recovery following optic neuritis (ON), but the respective trials have mostly been negative. The aim of this study was to determine whether disease-modifying treatment (DMT) following ON as first manifestation of relapsing-remitting mul...

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Autores principales: Pfeuffer, Steffen, Kerschke, Laura, Ruck, Tobias, Rolfes, Leoni, Pawlitzki, Marc, Albrecht, Philipp, Wiendl, Heinz, Meuth, Sven G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940774/
https://www.ncbi.nlm.nih.gov/pubmed/33747129
http://dx.doi.org/10.1177/1756286421997372
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author Pfeuffer, Steffen
Kerschke, Laura
Ruck, Tobias
Rolfes, Leoni
Pawlitzki, Marc
Albrecht, Philipp
Wiendl, Heinz
Meuth, Sven G.
author_facet Pfeuffer, Steffen
Kerschke, Laura
Ruck, Tobias
Rolfes, Leoni
Pawlitzki, Marc
Albrecht, Philipp
Wiendl, Heinz
Meuth, Sven G.
author_sort Pfeuffer, Steffen
collection PubMed
description BACKGROUND AND AIMS: Various attempts have been made to support recovery following optic neuritis (ON), but the respective trials have mostly been negative. The aim of this study was to determine whether disease-modifying treatment (DMT) following ON as first manifestation of relapsing-remitting multiple sclerosis influences long-term outcomes. METHODS: A total of 79 patients with ON were identified and evaluated at relapse, DMT induction, and 12 months following treatment induction with either glatiramer acetate (GLAT), interferon-beta (IFN), or teriflunomide (TRF). Low-contrast letter acuity (LCLA) and full-field visual-evoked potentials (FF-VEP) were compared between treatment groups using multivariable regression models. The impact of TRF treatment induction compared with IFN or GLAT following relapses outside the optic nerves was evaluated in an independent cohort of 122 patients. Magnetic resonance imaging (MRI) outcomes and rates of confirmed improvement of relapse-related disability were evaluated. RESULTS: TRF-treated patients exhibited higher LCLA and lower relative P100 latencies normalized to the fellow-eye. Findings were significant following covariate-adjustment by multivariable analyses. Cranial MRI lesion load as well as disability progression rates were not significantly different between groups. The cohort of patients following relapses other than ON showed no differences in confirmed improvement of disability. CONCLUSION: TRF treatment is associated with favorable outcomes regarding functional optic nerve recovery following ON in early multiple sclerosis.
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spelling pubmed-79407742021-03-18 Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis Pfeuffer, Steffen Kerschke, Laura Ruck, Tobias Rolfes, Leoni Pawlitzki, Marc Albrecht, Philipp Wiendl, Heinz Meuth, Sven G. Ther Adv Neurol Disord Original Research BACKGROUND AND AIMS: Various attempts have been made to support recovery following optic neuritis (ON), but the respective trials have mostly been negative. The aim of this study was to determine whether disease-modifying treatment (DMT) following ON as first manifestation of relapsing-remitting multiple sclerosis influences long-term outcomes. METHODS: A total of 79 patients with ON were identified and evaluated at relapse, DMT induction, and 12 months following treatment induction with either glatiramer acetate (GLAT), interferon-beta (IFN), or teriflunomide (TRF). Low-contrast letter acuity (LCLA) and full-field visual-evoked potentials (FF-VEP) were compared between treatment groups using multivariable regression models. The impact of TRF treatment induction compared with IFN or GLAT following relapses outside the optic nerves was evaluated in an independent cohort of 122 patients. Magnetic resonance imaging (MRI) outcomes and rates of confirmed improvement of relapse-related disability were evaluated. RESULTS: TRF-treated patients exhibited higher LCLA and lower relative P100 latencies normalized to the fellow-eye. Findings were significant following covariate-adjustment by multivariable analyses. Cranial MRI lesion load as well as disability progression rates were not significantly different between groups. The cohort of patients following relapses other than ON showed no differences in confirmed improvement of disability. CONCLUSION: TRF treatment is associated with favorable outcomes regarding functional optic nerve recovery following ON in early multiple sclerosis. SAGE Publications 2021-03-06 /pmc/articles/PMC7940774/ /pubmed/33747129 http://dx.doi.org/10.1177/1756286421997372 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Pfeuffer, Steffen
Kerschke, Laura
Ruck, Tobias
Rolfes, Leoni
Pawlitzki, Marc
Albrecht, Philipp
Wiendl, Heinz
Meuth, Sven G.
Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
title Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
title_full Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
title_fullStr Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
title_full_unstemmed Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
title_short Teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
title_sort teriflunomide treatment is associated with optic nerve recovery in early multiple sclerosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940774/
https://www.ncbi.nlm.nih.gov/pubmed/33747129
http://dx.doi.org/10.1177/1756286421997372
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