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Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis

BACKGROUND: Magnetic resonance imaging (MRI) markers for chronic active lesions in MS include slowly expanding lesions (SELs) and paramagnetic rim lesions (PRLs). OBJECTIVES: To identify the relationship between SELs and PRLs in MS, and their association with disability. METHODS: 61 people with MS (...

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Autores principales: Calvi, Alberto, Clarke, Margareta A, Prados, Ferran, Chard, Declan, Ciccarelli, Olga, Alberich, Manel, Pareto, Deborah, Rodríguez Barranco, Marta, Sastre-Garriga, Jaume, Tur, Carmen, Rovira, Alex, Barkhof, Frederik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972234/
https://www.ncbi.nlm.nih.gov/pubmed/36515487
http://dx.doi.org/10.1177/13524585221141964
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author Calvi, Alberto
Clarke, Margareta A
Prados, Ferran
Chard, Declan
Ciccarelli, Olga
Alberich, Manel
Pareto, Deborah
Rodríguez Barranco, Marta
Sastre-Garriga, Jaume
Tur, Carmen
Rovira, Alex
Barkhof, Frederik
author_facet Calvi, Alberto
Clarke, Margareta A
Prados, Ferran
Chard, Declan
Ciccarelli, Olga
Alberich, Manel
Pareto, Deborah
Rodríguez Barranco, Marta
Sastre-Garriga, Jaume
Tur, Carmen
Rovira, Alex
Barkhof, Frederik
author_sort Calvi, Alberto
collection PubMed
description BACKGROUND: Magnetic resonance imaging (MRI) markers for chronic active lesions in MS include slowly expanding lesions (SELs) and paramagnetic rim lesions (PRLs). OBJECTIVES: To identify the relationship between SELs and PRLs in MS, and their association with disability. METHODS: 61 people with MS (pwMS) followed retrospectively with MRI including baseline susceptibility-weighted imaging, and longitudinal T1 and T2-weighted scans. SELs were computed using deformation field maps; PRLs were visually identified. Mixed-effects models assessed differences in Expanded Disability Status Scale (EDSS) score changes between the group defined by the presence of SELs and or PRLs. RESULTS: The median follow-up time was 3.2 years. At baseline, out of 1492 lesions, 616 were classified as SELs, and 80 as PRLs. 92% of patients had ⩾ 1 SEL, 56% had ⩾ 1 PRL, while both were found in 51%. SELs compared to non-SELs were more likely to also be PRLs (7% vs. 4%, p = 0.027). PRL counts positively correlated with SEL counts (ρ= 0.28, p = 0.03). SEL + PRL + patients had greater increases in EDSS over time (beta = 0.15/year, 95% confidence interval (0.04, 0.27), p = 0.009) than SEL+PRL-patients. CONCLUSION: SELs are more numerous than PRLs in pwMS. Compared with either SELs or PRLs found in isolation, their joint occurrence was associated with greater clinical progression.
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spelling pubmed-99722342023-03-01 Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis Calvi, Alberto Clarke, Margareta A Prados, Ferran Chard, Declan Ciccarelli, Olga Alberich, Manel Pareto, Deborah Rodríguez Barranco, Marta Sastre-Garriga, Jaume Tur, Carmen Rovira, Alex Barkhof, Frederik Mult Scler Original Research Papers BACKGROUND: Magnetic resonance imaging (MRI) markers for chronic active lesions in MS include slowly expanding lesions (SELs) and paramagnetic rim lesions (PRLs). OBJECTIVES: To identify the relationship between SELs and PRLs in MS, and their association with disability. METHODS: 61 people with MS (pwMS) followed retrospectively with MRI including baseline susceptibility-weighted imaging, and longitudinal T1 and T2-weighted scans. SELs were computed using deformation field maps; PRLs were visually identified. Mixed-effects models assessed differences in Expanded Disability Status Scale (EDSS) score changes between the group defined by the presence of SELs and or PRLs. RESULTS: The median follow-up time was 3.2 years. At baseline, out of 1492 lesions, 616 were classified as SELs, and 80 as PRLs. 92% of patients had ⩾ 1 SEL, 56% had ⩾ 1 PRL, while both were found in 51%. SELs compared to non-SELs were more likely to also be PRLs (7% vs. 4%, p = 0.027). PRL counts positively correlated with SEL counts (ρ= 0.28, p = 0.03). SEL + PRL + patients had greater increases in EDSS over time (beta = 0.15/year, 95% confidence interval (0.04, 0.27), p = 0.009) than SEL+PRL-patients. CONCLUSION: SELs are more numerous than PRLs in pwMS. Compared with either SELs or PRLs found in isolation, their joint occurrence was associated with greater clinical progression. SAGE Publications 2022-12-14 2023-03 /pmc/articles/PMC9972234/ /pubmed/36515487 http://dx.doi.org/10.1177/13524585221141964 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any 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
Calvi, Alberto
Clarke, Margareta A
Prados, Ferran
Chard, Declan
Ciccarelli, Olga
Alberich, Manel
Pareto, Deborah
Rodríguez Barranco, Marta
Sastre-Garriga, Jaume
Tur, Carmen
Rovira, Alex
Barkhof, Frederik
Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
title Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
title_full Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
title_fullStr Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
title_full_unstemmed Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
title_short Relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
title_sort relationship between paramagnetic rim lesions and slowly expanding lesions in multiple sclerosis
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972234/
https://www.ncbi.nlm.nih.gov/pubmed/36515487
http://dx.doi.org/10.1177/13524585221141964
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