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Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?

OBJECTIVE: The objective of the study was to determine whether early infratentorial and/or spinal cord lesions are long-term cumulative predictors of disability progression in multiple sclerosis (MS). METHODS: We selected 153 MS patients from the longitudinal Amsterdam MS cohort. Lesion analysis was...

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Autores principales: Dekker, Iris, Sombekke, Madeleine H, Balk, Lisanne J, Moraal, Bastiaan, Geurts, Jeroen JG, Barkhof, Frederik, Uitdehaag, Bernard MJ, Killestein, Joep, Wattjes, Mike P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7543019/
https://www.ncbi.nlm.nih.gov/pubmed/31373535
http://dx.doi.org/10.1177/1352458519864933
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author Dekker, Iris
Sombekke, Madeleine H
Balk, Lisanne J
Moraal, Bastiaan
Geurts, Jeroen JG
Barkhof, Frederik
Uitdehaag, Bernard MJ
Killestein, Joep
Wattjes, Mike P
author_facet Dekker, Iris
Sombekke, Madeleine H
Balk, Lisanne J
Moraal, Bastiaan
Geurts, Jeroen JG
Barkhof, Frederik
Uitdehaag, Bernard MJ
Killestein, Joep
Wattjes, Mike P
author_sort Dekker, Iris
collection PubMed
description OBJECTIVE: The objective of the study was to determine whether early infratentorial and/or spinal cord lesions are long-term cumulative predictors of disability progression in multiple sclerosis (MS). METHODS: We selected 153 MS patients from the longitudinal Amsterdam MS cohort. Lesion analysis was performed at baseline and year 2. Disability progression after 6 and 11 years was measured using the Expanded Disability Status Scale (EDSS) and EDSS-plus (including 25-foot walk and 9-hole peg test). Patients with spinal cord or infratentorial lesions were compared for the risk of 6- and 11-year disability progression to patients without spinal cord or infratentorial lesions, respectively. Subsequently, patients with lesions on both locations were compared to patients with only spinal cord or only infratentorial lesions. RESULTS: Baseline spinal cord lesions show a higher risk of 6-year EDSS progression (odds ratio (OR): 3.6, p = 0.007) and EDSS-plus progression (OR: 2.5, p = 0.028) and 11-year EDSS progression (OR: 2.8, p = 0.047). Patients with both infratentorial and spinal cord lesions did not have a higher risk of 6-year disability progression than patients with only infratentorial or only spinal cord lesions. CONCLUSION: The presence of early spinal cord lesions seems to be a dominant risk factor of disability progression. Simultaneous presence of early infratentorial and spinal cord lesions did not undisputedly predict disability progression.
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spelling pubmed-75430192020-10-14 Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability? Dekker, Iris Sombekke, Madeleine H Balk, Lisanne J Moraal, Bastiaan Geurts, Jeroen JG Barkhof, Frederik Uitdehaag, Bernard MJ Killestein, Joep Wattjes, Mike P Mult Scler Original Research Papers OBJECTIVE: The objective of the study was to determine whether early infratentorial and/or spinal cord lesions are long-term cumulative predictors of disability progression in multiple sclerosis (MS). METHODS: We selected 153 MS patients from the longitudinal Amsterdam MS cohort. Lesion analysis was performed at baseline and year 2. Disability progression after 6 and 11 years was measured using the Expanded Disability Status Scale (EDSS) and EDSS-plus (including 25-foot walk and 9-hole peg test). Patients with spinal cord or infratentorial lesions were compared for the risk of 6- and 11-year disability progression to patients without spinal cord or infratentorial lesions, respectively. Subsequently, patients with lesions on both locations were compared to patients with only spinal cord or only infratentorial lesions. RESULTS: Baseline spinal cord lesions show a higher risk of 6-year EDSS progression (odds ratio (OR): 3.6, p = 0.007) and EDSS-plus progression (OR: 2.5, p = 0.028) and 11-year EDSS progression (OR: 2.8, p = 0.047). Patients with both infratentorial and spinal cord lesions did not have a higher risk of 6-year disability progression than patients with only infratentorial or only spinal cord lesions. CONCLUSION: The presence of early spinal cord lesions seems to be a dominant risk factor of disability progression. Simultaneous presence of early infratentorial and spinal cord lesions did not undisputedly predict disability progression. SAGE Publications 2019-08-02 2020-10 /pmc/articles/PMC7543019/ /pubmed/31373535 http://dx.doi.org/10.1177/1352458519864933 Text en © The Author(s), 2019 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
Balk, Lisanne J
Moraal, Bastiaan
Geurts, Jeroen JG
Barkhof, Frederik
Uitdehaag, Bernard MJ
Killestein, Joep
Wattjes, Mike P
Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?
title Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?
title_full Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?
title_fullStr Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?
title_full_unstemmed Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?
title_short Infratentorial and spinal cord lesions: Cumulative predictors of long-term disability?
title_sort infratentorial and spinal cord lesions: cumulative predictors of long-term disability?
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7543019/
https://www.ncbi.nlm.nih.gov/pubmed/31373535
http://dx.doi.org/10.1177/1352458519864933
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