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Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis

The information provided by a person with multiple sclerosis (MS) may anticipate changes in the course of the disease. To explore the role of a set of standardized patient-reported outcomes (PRO) in predicting disability progression in MS an observational study was conducted in two cohorts of 30 and...

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Autores principales: Gil-Perotin, S., Bernad, L., Reddam, S., Ferrer-Pardo, C., Navarro-Quevedo, S., Solís-Tarazona, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617913/
https://www.ncbi.nlm.nih.gov/pubmed/36309532
http://dx.doi.org/10.1038/s41598-022-23088-x
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author Gil-Perotin, S.
Bernad, L.
Reddam, S.
Ferrer-Pardo, C.
Navarro-Quevedo, S.
Solís-Tarazona, L.
author_facet Gil-Perotin, S.
Bernad, L.
Reddam, S.
Ferrer-Pardo, C.
Navarro-Quevedo, S.
Solís-Tarazona, L.
author_sort Gil-Perotin, S.
collection PubMed
description The information provided by a person with multiple sclerosis (MS) may anticipate changes in the course of the disease. To explore the role of a set of standardized patient-reported outcomes (PRO) in predicting disability progression in MS an observational study was conducted in two cohorts of 30 and 86 persons with progressive MS (pwPMS) and relapsing MS (pwRMS), respectively. The associations between baseline clinical, biochemical variables and results on MS quality of life scale (MusiQol), Modified Fatigue Impact Scale (MFIS) and Beck Depression Inventory II (BDI-II) were analyzed. The progression of disability after 2 years of follow-up in pwRMS was investigated. We show that PRO differentiated pwRMS and pwPMS cohorts with lower MusiQoL and higher MFIS and BDI-II scores in the latter. Only MFIS was correlated with disability in pwRMS and high scores in the physical MFIS domain associated with worse performance in 9HPT, and a trend in T25FW and SDMT. Instead, the cognitive MFIS domain was correlated with CHI3L1 in cerebrospinal fluid, a biomarker of progression. At the end of the study, global MFIS and BDI-II were found to be independent risk factors for disability independent of relapse. Although all PRO measures explored were altered in pwPMS, baseline MFIS discriminated current and prospective disability in pwRMS, identifying patients at risk of progression.
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spelling pubmed-96179132022-10-31 Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis Gil-Perotin, S. Bernad, L. Reddam, S. Ferrer-Pardo, C. Navarro-Quevedo, S. Solís-Tarazona, L. Sci Rep Article The information provided by a person with multiple sclerosis (MS) may anticipate changes in the course of the disease. To explore the role of a set of standardized patient-reported outcomes (PRO) in predicting disability progression in MS an observational study was conducted in two cohorts of 30 and 86 persons with progressive MS (pwPMS) and relapsing MS (pwRMS), respectively. The associations between baseline clinical, biochemical variables and results on MS quality of life scale (MusiQol), Modified Fatigue Impact Scale (MFIS) and Beck Depression Inventory II (BDI-II) were analyzed. The progression of disability after 2 years of follow-up in pwRMS was investigated. We show that PRO differentiated pwRMS and pwPMS cohorts with lower MusiQoL and higher MFIS and BDI-II scores in the latter. Only MFIS was correlated with disability in pwRMS and high scores in the physical MFIS domain associated with worse performance in 9HPT, and a trend in T25FW and SDMT. Instead, the cognitive MFIS domain was correlated with CHI3L1 in cerebrospinal fluid, a biomarker of progression. At the end of the study, global MFIS and BDI-II were found to be independent risk factors for disability independent of relapse. Although all PRO measures explored were altered in pwPMS, baseline MFIS discriminated current and prospective disability in pwRMS, identifying patients at risk of progression. Nature Publishing Group UK 2022-10-29 /pmc/articles/PMC9617913/ /pubmed/36309532 http://dx.doi.org/10.1038/s41598-022-23088-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gil-Perotin, S.
Bernad, L.
Reddam, S.
Ferrer-Pardo, C.
Navarro-Quevedo, S.
Solís-Tarazona, L.
Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
title Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
title_full Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
title_fullStr Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
title_full_unstemmed Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
title_short Patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
title_sort patient's perspective in clinical practice to assess and predict disability in multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617913/
https://www.ncbi.nlm.nih.gov/pubmed/36309532
http://dx.doi.org/10.1038/s41598-022-23088-x
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