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Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis

OBJECTIVE: The objective of this article is to investigate potential clinical and MRI predictors of long-term outcomes in multiple sclerosis (MS). METHODS: This was a post hoc analysis using data from all 382 patients in the PRISMS long-term follow-up (LTFU) study collected up to eight years after r...

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Autores principales: Traboulsee, Anthony L, Cornelisseª, Peter, Sandberg-Wollheim, Magnhild, Uitdehaag, Bernard MJ, Kappos, Ludwig, Jongen, Peter J, Constantinescu, Cris S, di Cantogno, Elisabetta Verdun, Li, David KB
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433509/
https://www.ncbi.nlm.nih.gov/pubmed/28607737
http://dx.doi.org/10.1177/2055217316666406
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author Traboulsee, Anthony L
Cornelisseª, Peter
Sandberg-Wollheim, Magnhild
Uitdehaag, Bernard MJ
Kappos, Ludwig
Jongen, Peter J
Constantinescu, Cris S
di Cantogno, Elisabetta Verdun
Li, David KB
author_facet Traboulsee, Anthony L
Cornelisseª, Peter
Sandberg-Wollheim, Magnhild
Uitdehaag, Bernard MJ
Kappos, Ludwig
Jongen, Peter J
Constantinescu, Cris S
di Cantogno, Elisabetta Verdun
Li, David KB
author_sort Traboulsee, Anthony L
collection PubMed
description OBJECTIVE: The objective of this article is to investigate potential clinical and MRI predictors of long-term outcomes in multiple sclerosis (MS). METHODS: This was a post hoc analysis using data from all 382 patients in the PRISMS long-term follow-up (LTFU) study collected up to eight years after randomisation. An additional analysis was performed including only those patients originally randomised to receive early subcutaneous interferon (IFN) β-1a (n = 259). Baseline/prestudy variables, indicators of early clinical and MRI activity (baseline to month 24), and indicators of IFN β-1a treatment exposure (including medication possession ratio (MPR)) were investigated as candidate prognostic factors for outcomes measured from baseline and from month 24 to LTFU. Explanatory variables identified from univariate regression models (p ≤ 0.15) were selected for inclusion in stepwise multiple regression models. RESULTS: Candidate prognostic factors selected by the univariate analysis (p ≤ 0.15) included age, MS duration, baseline brain volume, EDSS score, and log(T2 burden of disease (BOD)). In most of the multivariate regression models applied, higher baseline brain volume and MPR predicted better long-term clinical outcomes, while higher baseline and greater early increase in EDSS score predicted worse outcomes. CONCLUSION: Identification of markers that may be prognostic for long-term disability could help identify MS patients at higher risk of disability progression.
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spelling pubmed-54335092017-06-12 Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis Traboulsee, Anthony L Cornelisseª, Peter Sandberg-Wollheim, Magnhild Uitdehaag, Bernard MJ Kappos, Ludwig Jongen, Peter J Constantinescu, Cris S di Cantogno, Elisabetta Verdun Li, David KB Mult Scler J Exp Transl Clin Original Article OBJECTIVE: The objective of this article is to investigate potential clinical and MRI predictors of long-term outcomes in multiple sclerosis (MS). METHODS: This was a post hoc analysis using data from all 382 patients in the PRISMS long-term follow-up (LTFU) study collected up to eight years after randomisation. An additional analysis was performed including only those patients originally randomised to receive early subcutaneous interferon (IFN) β-1a (n = 259). Baseline/prestudy variables, indicators of early clinical and MRI activity (baseline to month 24), and indicators of IFN β-1a treatment exposure (including medication possession ratio (MPR)) were investigated as candidate prognostic factors for outcomes measured from baseline and from month 24 to LTFU. Explanatory variables identified from univariate regression models (p ≤ 0.15) were selected for inclusion in stepwise multiple regression models. RESULTS: Candidate prognostic factors selected by the univariate analysis (p ≤ 0.15) included age, MS duration, baseline brain volume, EDSS score, and log(T2 burden of disease (BOD)). In most of the multivariate regression models applied, higher baseline brain volume and MPR predicted better long-term clinical outcomes, while higher baseline and greater early increase in EDSS score predicted worse outcomes. CONCLUSION: Identification of markers that may be prognostic for long-term disability could help identify MS patients at higher risk of disability progression. SAGE Publications 2016-09-06 /pmc/articles/PMC5433509/ /pubmed/28607737 http://dx.doi.org/10.1177/2055217316666406 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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 page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Traboulsee, Anthony L
Cornelisseª, Peter
Sandberg-Wollheim, Magnhild
Uitdehaag, Bernard MJ
Kappos, Ludwig
Jongen, Peter J
Constantinescu, Cris S
di Cantogno, Elisabetta Verdun
Li, David KB
Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
title Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
title_full Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
title_fullStr Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
title_full_unstemmed Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
title_short Prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
title_sort prognostic factors for long-term outcomes in relapsing–remitting multiple sclerosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433509/
https://www.ncbi.nlm.nih.gov/pubmed/28607737
http://dx.doi.org/10.1177/2055217316666406
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