Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin

Abstract Multiple sclerosis (MS) is a common autoimmune disease of the central nervous system, causing neurological disability in young adults. A growing understanding of its immunopathogenesis has led to an expanding array of therapies. Notable new advances in disease-modifying therapies for relaps...

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Main Authors: Alexis Demas, Jean-Philippe Cochin, Clémence Hardy, Yvan Vaschalde, Bertrand Bourre, Pierre Labauge
Format: Article
Language:English
Published: Adis, Springer Healthcare 2019-12-01
Series:Neurology and Therapy
Subjects:
Online Access:https://doi.org/10.1007/s40120-019-00175-2
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author Alexis Demas
Jean-Philippe Cochin
Clémence Hardy
Yvan Vaschalde
Bertrand Bourre
Pierre Labauge
author_facet Alexis Demas
Jean-Philippe Cochin
Clémence Hardy
Yvan Vaschalde
Bertrand Bourre
Pierre Labauge
author_sort Alexis Demas
collection DOAJ
description Abstract Multiple sclerosis (MS) is a common autoimmune disease of the central nervous system, causing neurological disability in young adults. A growing understanding of its immunopathogenesis has led to an expanding array of therapies. Notable new advances in disease-modifying therapies for relapsing forms of multiple sclerosis that are based on anti-inflammatory activity have recently been developed. Management of progressive MS is still challenging. Data published in 2014 suggested that daily high doses of biotin, a vitamin involved in myelin synthesis, might have a beneficial impact on disability and progression in progressive MS. However, some patients worsened while on biotin without any clear explanation for this effect. We report the case of a 41-year-old patient suffering from primary progressive (PP) MS who presented after 16 months of treatment with high doses of biotin (QIZENDAY) with worsening of his Expanding Disability Status Scale (EDSS) score and the appearance of a symptomatic new T2 pseudo-tumoural lesion on brain magnetic resonance imaging (MRI), suggestive of tardive inflammatory reactivation possibly due to the biotin. The newer and more effective therapies for MS are, however, associated with risks that necessitate an active management strategy and continuous vigilance. Physicians should be aware of iatrogenic neurological complications and the possible paradoxical effects of biotin. Future treatment approaches to progressive MS must include identification of a biomarker of disease activity. The study of neurofilaments in the cerebrospinal fluid (CSF) and the serum could be of interest when determining the optimal treatment strategy.
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spelling doaj.art-b5a5a827026546a79947c24aa5f59cbc2024-04-14T11:33:31ZengAdis, Springer HealthcareNeurology and Therapy2193-82532193-65362019-12-019118118510.1007/s40120-019-00175-2Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with BiotinAlexis Demas0Jean-Philippe Cochin1Clémence Hardy2Yvan Vaschalde3Bertrand Bourre4Pierre Labauge5Department of Neurology, Hospital Jacques MonodDepartment of Neurology, Hospital Jacques MonodDepartment of Neurology, Hospital Jacques MonodDepartment of Neurology, Hospital Jacques MonodDepartment of Neurology, Rouen University Hospital, University of RouenDepartment of Neurology, Reference Centre for Adult Leukodystrophies, Montpellier University Hospital, Montpellier, FranceAbstract Multiple sclerosis (MS) is a common autoimmune disease of the central nervous system, causing neurological disability in young adults. A growing understanding of its immunopathogenesis has led to an expanding array of therapies. Notable new advances in disease-modifying therapies for relapsing forms of multiple sclerosis that are based on anti-inflammatory activity have recently been developed. Management of progressive MS is still challenging. Data published in 2014 suggested that daily high doses of biotin, a vitamin involved in myelin synthesis, might have a beneficial impact on disability and progression in progressive MS. However, some patients worsened while on biotin without any clear explanation for this effect. We report the case of a 41-year-old patient suffering from primary progressive (PP) MS who presented after 16 months of treatment with high doses of biotin (QIZENDAY) with worsening of his Expanding Disability Status Scale (EDSS) score and the appearance of a symptomatic new T2 pseudo-tumoural lesion on brain magnetic resonance imaging (MRI), suggestive of tardive inflammatory reactivation possibly due to the biotin. The newer and more effective therapies for MS are, however, associated with risks that necessitate an active management strategy and continuous vigilance. Physicians should be aware of iatrogenic neurological complications and the possible paradoxical effects of biotin. Future treatment approaches to progressive MS must include identification of a biomarker of disease activity. The study of neurofilaments in the cerebrospinal fluid (CSF) and the serum could be of interest when determining the optimal treatment strategy.https://doi.org/10.1007/s40120-019-00175-2Adverse drug reactionBiotinMRIMultiple sclerosisPseudo-tumoral lesion
spellingShingle Alexis Demas
Jean-Philippe Cochin
Clémence Hardy
Yvan Vaschalde
Bertrand Bourre
Pierre Labauge
Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin
Neurology and Therapy
Adverse drug reaction
Biotin
MRI
Multiple sclerosis
Pseudo-tumoral lesion
title Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin
title_full Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin
title_fullStr Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin
title_full_unstemmed Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin
title_short Tardive Reactivation of Progressive Multiple Sclerosis During Treatment with Biotin
title_sort tardive reactivation of progressive multiple sclerosis during treatment with biotin
topic Adverse drug reaction
Biotin
MRI
Multiple sclerosis
Pseudo-tumoral lesion
url https://doi.org/10.1007/s40120-019-00175-2
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