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Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis

BACKGROUND: The presence of asymptomatic spinal cord (SC) lesions in patients with clinically isolated syndrome (CIS) or relapsing-remitting multiple sclerosis (RRMS) predicts conversion to clinically definite multiple sclerosis (CDMS). The relation between asymptomatic SC abnormalities and disabili...

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Autores principales: Dekker, Iris, Sombekke, Madeleine H, Witte, Birgit I, Geurts, Jeroen JG, Barkhof, Frederik, Uitdehaag, Bernard MJ, Killestein, Joep, Wattjes, Mike P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881784/
https://www.ncbi.nlm.nih.gov/pubmed/29106327
http://dx.doi.org/10.1177/1352458517736147
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author Dekker, Iris
Sombekke, Madeleine H
Witte, Birgit I
Geurts, Jeroen JG
Barkhof, Frederik
Uitdehaag, Bernard MJ
Killestein, Joep
Wattjes, Mike P
author_facet Dekker, Iris
Sombekke, Madeleine H
Witte, Birgit I
Geurts, Jeroen JG
Barkhof, Frederik
Uitdehaag, Bernard MJ
Killestein, Joep
Wattjes, Mike P
author_sort Dekker, Iris
collection PubMed
description BACKGROUND: The presence of asymptomatic spinal cord (SC) lesions in patients with clinically isolated syndrome (CIS) or relapsing-remitting multiple sclerosis (RRMS) predicts conversion to clinically definite multiple sclerosis (CDMS). The relation between asymptomatic SC abnormalities and disability progression warrants further investigation. OBJECTIVE: To determine the prognostic value of asymptomatic SC lesions in CIS and early RRMS with respect to the time to disability development. METHODS: Clinical and demographic data, brain and SC magnetic resonance imaging (MRI) were collected of CIS or early RRMS patients. Two main analyses were performed. For the first analysis, patients were divided into two groups: (1) patients with asymptomatic SC lesions and (2) patients without SC lesions and patients with symptomatic SC lesions. The second analysis excluded patients with symptomatic SC lesions. Incidence curves were used to analyse differences between these groups in time to the development of disability and time to a second relapse. RESULTS: A total of 178 patients were included, and 42 patients (23.6%) had asymptomatic SC lesions. No significant differences were found on the time to disability development or the time to a second event. CONCLUSION: Asymptomatic SC lesions early in the disease course do not predict the time to disability development in patients diagnosed with CIS or early RRMS.
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spelling pubmed-58817842018-04-13 Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis Dekker, Iris Sombekke, Madeleine H Witte, Birgit I Geurts, Jeroen JG Barkhof, Frederik Uitdehaag, Bernard MJ Killestein, Joep Wattjes, Mike P Mult Scler Original Research Papers BACKGROUND: The presence of asymptomatic spinal cord (SC) lesions in patients with clinically isolated syndrome (CIS) or relapsing-remitting multiple sclerosis (RRMS) predicts conversion to clinically definite multiple sclerosis (CDMS). The relation between asymptomatic SC abnormalities and disability progression warrants further investigation. OBJECTIVE: To determine the prognostic value of asymptomatic SC lesions in CIS and early RRMS with respect to the time to disability development. METHODS: Clinical and demographic data, brain and SC magnetic resonance imaging (MRI) were collected of CIS or early RRMS patients. Two main analyses were performed. For the first analysis, patients were divided into two groups: (1) patients with asymptomatic SC lesions and (2) patients without SC lesions and patients with symptomatic SC lesions. The second analysis excluded patients with symptomatic SC lesions. Incidence curves were used to analyse differences between these groups in time to the development of disability and time to a second relapse. RESULTS: A total of 178 patients were included, and 42 patients (23.6%) had asymptomatic SC lesions. No significant differences were found on the time to disability development or the time to a second event. CONCLUSION: Asymptomatic SC lesions early in the disease course do not predict the time to disability development in patients diagnosed with CIS or early RRMS. SAGE Publications 2017-11-06 2018-04 /pmc/articles/PMC5881784/ /pubmed/29106327 http://dx.doi.org/10.1177/1352458517736147 Text en © The Author(s), 2017 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.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 Papers
Dekker, Iris
Sombekke, Madeleine H
Witte, Birgit I
Geurts, Jeroen JG
Barkhof, Frederik
Uitdehaag, Bernard MJ
Killestein, Joep
Wattjes, Mike P
Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
title Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
title_full Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
title_fullStr Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
title_full_unstemmed Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
title_short Asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
title_sort asymptomatic spinal cord lesions do not predict the time to disability in patients with early multiple sclerosis
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881784/
https://www.ncbi.nlm.nih.gov/pubmed/29106327
http://dx.doi.org/10.1177/1352458517736147
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