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Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting

PURPOSE: Rim lesions, characterised by a paramagnetic rim on susceptibility-based MRI, have been suggested to reflect chronic inflammatory demyelination in multiple sclerosis (MS) patients. Here, we assess, through susceptibility-weighted imaging (SWI), the prevalence, longitudinal volume evolution...

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Autores principales: Ng Kee Kwong, Koy Chong, Mollison, Daisy, Meijboom, Rozanna, York, Elizabeth N., Kampaite, Agniete, Martin, Sarah-Jane, Hunt, David P. J., Thrippleton, Michael J., Chandran, Siddharthan, Waldman, Adam D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724059/
https://www.ncbi.nlm.nih.gov/pubmed/34664112
http://dx.doi.org/10.1007/s00234-021-02768-x
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author Ng Kee Kwong, Koy Chong
Mollison, Daisy
Meijboom, Rozanna
York, Elizabeth N.
Kampaite, Agniete
Martin, Sarah-Jane
Hunt, David P. J.
Thrippleton, Michael J.
Chandran, Siddharthan
Waldman, Adam D.
author_facet Ng Kee Kwong, Koy Chong
Mollison, Daisy
Meijboom, Rozanna
York, Elizabeth N.
Kampaite, Agniete
Martin, Sarah-Jane
Hunt, David P. J.
Thrippleton, Michael J.
Chandran, Siddharthan
Waldman, Adam D.
author_sort Ng Kee Kwong, Koy Chong
collection PubMed
description PURPOSE: Rim lesions, characterised by a paramagnetic rim on susceptibility-based MRI, have been suggested to reflect chronic inflammatory demyelination in multiple sclerosis (MS) patients. Here, we assess, through susceptibility-weighted imaging (SWI), the prevalence, longitudinal volume evolution and clinical associations of rim lesions in subjects with early relapsing–remitting MS (RRMS). METHODS: Subjects (n = 44) with recently diagnosed RRMS underwent 3 T MRI at baseline (M0) and 1 year (M12) as part of a multi-centre study. SWI was acquired at M12 using a 3D segmented gradient-echo echo-planar imaging sequence. Rim lesions identified on SWI were manually segmented on FLAIR images at both time points for volumetric analysis. RESULTS: Twelve subjects (27%) had at least one rim lesion at M12. A linear mixed-effects model, with ‘subject’ as a random factor, revealed mixed evidence for the difference in longitudinal volume change between rim lesions and non-rim lesions (p = 0.0350 and p = 0.0556 for subjects with and without rim lesions, respectively). All 25 rim lesions identified showed T1-weighted hypointense signal. Subjects with and without rim lesions did not differ significantly with respect to age, disease duration or clinical measures of disability (p > 0.05). CONCLUSION: We demonstrate that rim lesions are detectable in early-stage RRMS on 3 T MRI across multiple centres, although their relationship to lesion enlargement is equivocal in this small cohort. Identification of SWI rims was subjective. Agreed criteria for defining rim lesions and their further validation as a biomarker of chronic inflammation are required for translation of SWI into routine MS clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00234-021-02768-x.
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spelling pubmed-87240592022-01-13 Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting Ng Kee Kwong, Koy Chong Mollison, Daisy Meijboom, Rozanna York, Elizabeth N. Kampaite, Agniete Martin, Sarah-Jane Hunt, David P. J. Thrippleton, Michael J. Chandran, Siddharthan Waldman, Adam D. Neuroradiology Diagnostic Neuroradiology PURPOSE: Rim lesions, characterised by a paramagnetic rim on susceptibility-based MRI, have been suggested to reflect chronic inflammatory demyelination in multiple sclerosis (MS) patients. Here, we assess, through susceptibility-weighted imaging (SWI), the prevalence, longitudinal volume evolution and clinical associations of rim lesions in subjects with early relapsing–remitting MS (RRMS). METHODS: Subjects (n = 44) with recently diagnosed RRMS underwent 3 T MRI at baseline (M0) and 1 year (M12) as part of a multi-centre study. SWI was acquired at M12 using a 3D segmented gradient-echo echo-planar imaging sequence. Rim lesions identified on SWI were manually segmented on FLAIR images at both time points for volumetric analysis. RESULTS: Twelve subjects (27%) had at least one rim lesion at M12. A linear mixed-effects model, with ‘subject’ as a random factor, revealed mixed evidence for the difference in longitudinal volume change between rim lesions and non-rim lesions (p = 0.0350 and p = 0.0556 for subjects with and without rim lesions, respectively). All 25 rim lesions identified showed T1-weighted hypointense signal. Subjects with and without rim lesions did not differ significantly with respect to age, disease duration or clinical measures of disability (p > 0.05). CONCLUSION: We demonstrate that rim lesions are detectable in early-stage RRMS on 3 T MRI across multiple centres, although their relationship to lesion enlargement is equivocal in this small cohort. Identification of SWI rims was subjective. Agreed criteria for defining rim lesions and their further validation as a biomarker of chronic inflammation are required for translation of SWI into routine MS clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00234-021-02768-x. Springer Berlin Heidelberg 2021-10-19 2022 /pmc/articles/PMC8724059/ /pubmed/34664112 http://dx.doi.org/10.1007/s00234-021-02768-x Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Diagnostic Neuroradiology
Ng Kee Kwong, Koy Chong
Mollison, Daisy
Meijboom, Rozanna
York, Elizabeth N.
Kampaite, Agniete
Martin, Sarah-Jane
Hunt, David P. J.
Thrippleton, Michael J.
Chandran, Siddharthan
Waldman, Adam D.
Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting
title Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting
title_full Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting
title_fullStr Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting
title_full_unstemmed Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting
title_short Rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 T-based susceptibility-weighted imaging in a multi-institutional setting
title_sort rim lesions are demonstrated in early relapsing–remitting multiple sclerosis using 3 t-based susceptibility-weighted imaging in a multi-institutional setting
topic Diagnostic Neuroradiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724059/
https://www.ncbi.nlm.nih.gov/pubmed/34664112
http://dx.doi.org/10.1007/s00234-021-02768-x
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