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Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis

BACKGROUND: Paramagnetic rim lesions (PRLs) and slowly expanding lesions (SELs) have been posited as markers of chronic active lesions (CALs). OBJECTIVE: To assess the lesion-level concordance of PRLs and SELs in MS and to characterize changes in brain tissue integrity in CALs over time. METHODS: MR...

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Autores principales: Elliott, Colm, Rudko, David A, Arnold, Douglas L, Fetco, Dumitru, Elkady, Ahmed M, Araujo, David, Zhu, Bing, Gafson, Arie, Tian, Zhe, Belachew, Shibeshih, Bradley, Daniel P, Fisher, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176750/
https://www.ncbi.nlm.nih.gov/pubmed/37036134
http://dx.doi.org/10.1177/13524585231162262
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author Elliott, Colm
Rudko, David A
Arnold, Douglas L
Fetco, Dumitru
Elkady, Ahmed M
Araujo, David
Zhu, Bing
Gafson, Arie
Tian, Zhe
Belachew, Shibeshih
Bradley, Daniel P
Fisher, Elizabeth
author_facet Elliott, Colm
Rudko, David A
Arnold, Douglas L
Fetco, Dumitru
Elkady, Ahmed M
Araujo, David
Zhu, Bing
Gafson, Arie
Tian, Zhe
Belachew, Shibeshih
Bradley, Daniel P
Fisher, Elizabeth
author_sort Elliott, Colm
collection PubMed
description BACKGROUND: Paramagnetic rim lesions (PRLs) and slowly expanding lesions (SELs) have been posited as markers of chronic active lesions (CALs). OBJECTIVE: To assess the lesion-level concordance of PRLs and SELs in MS and to characterize changes in brain tissue integrity in CALs over time. METHODS: MRIs were analyzed from a substudy of AFFINITY [NCT03222973], a phase 2 trial of opicinumab in relapsing MS. Assessments included (1) identification of SELs based on longitudinal MRIs over 72 weeks, and identification of PRLs on susceptibility-weighted imaging (SWI) filtered phase images at week 72; (2) evaluation of subject-level correlation of SEL and PRL counts, volumes, and degree of lesion-level overlap between SELs and PRLs; and (3) characterization of tissue integrity over time in overlapping and non-overlapping SELs and PRLs. RESULTS: In 41 subjects, 119 chronic PRLs and 267 SELs were detected. Of 119 (39.5%) chronic PRLs, 47 co-localized with a SEL; 46/267 (17.2%) SELs co-localized with a PRL. PRLs co-localized with SELs showed expansion and worsening microstructural damage over time. SELs with and without co-localization with PRLs showed ongoing tissue damage. CONCLUSIONS: Chronic MS lesions identified as both PRL and SEL were associated with the most severe accumulation of tissue damage. TRIAL REGISTRATION: AFFINITY [NCT03222973].
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spelling pubmed-101767502023-05-13 Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis Elliott, Colm Rudko, David A Arnold, Douglas L Fetco, Dumitru Elkady, Ahmed M Araujo, David Zhu, Bing Gafson, Arie Tian, Zhe Belachew, Shibeshih Bradley, Daniel P Fisher, Elizabeth Mult Scler Original Research Papers BACKGROUND: Paramagnetic rim lesions (PRLs) and slowly expanding lesions (SELs) have been posited as markers of chronic active lesions (CALs). OBJECTIVE: To assess the lesion-level concordance of PRLs and SELs in MS and to characterize changes in brain tissue integrity in CALs over time. METHODS: MRIs were analyzed from a substudy of AFFINITY [NCT03222973], a phase 2 trial of opicinumab in relapsing MS. Assessments included (1) identification of SELs based on longitudinal MRIs over 72 weeks, and identification of PRLs on susceptibility-weighted imaging (SWI) filtered phase images at week 72; (2) evaluation of subject-level correlation of SEL and PRL counts, volumes, and degree of lesion-level overlap between SELs and PRLs; and (3) characterization of tissue integrity over time in overlapping and non-overlapping SELs and PRLs. RESULTS: In 41 subjects, 119 chronic PRLs and 267 SELs were detected. Of 119 (39.5%) chronic PRLs, 47 co-localized with a SEL; 46/267 (17.2%) SELs co-localized with a PRL. PRLs co-localized with SELs showed expansion and worsening microstructural damage over time. SELs with and without co-localization with PRLs showed ongoing tissue damage. CONCLUSIONS: Chronic MS lesions identified as both PRL and SEL were associated with the most severe accumulation of tissue damage. TRIAL REGISTRATION: AFFINITY [NCT03222973]. SAGE Publications 2023-04-10 2023-05 /pmc/articles/PMC10176750/ /pubmed/37036134 http://dx.doi.org/10.1177/13524585231162262 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://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 page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Papers
Elliott, Colm
Rudko, David A
Arnold, Douglas L
Fetco, Dumitru
Elkady, Ahmed M
Araujo, David
Zhu, Bing
Gafson, Arie
Tian, Zhe
Belachew, Shibeshih
Bradley, Daniel P
Fisher, Elizabeth
Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
title Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
title_full Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
title_fullStr Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
title_full_unstemmed Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
title_short Lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
title_sort lesion-level correspondence and longitudinal properties of paramagnetic rim and slowly expanding lesions in multiple sclerosis
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176750/
https://www.ncbi.nlm.nih.gov/pubmed/37036134
http://dx.doi.org/10.1177/13524585231162262
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