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Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands

Oligoclonal IgG bands (OCB) in cerebrospinal fluid (CSF) are important in diagnosis of multiple sclerosis (MS). We evaluated the MRI features of clinically definite MS subjects with and without CSF-OCB. Relapsing MS subjects were recruited from a prospective registry in a university center. CSF-OCB...

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Autores principales: Zhao, Lin, Abrigo, Jill, Chen, Qianyun, Au, Cheryl, Ng, Angel, Fan, Ping, Mok, Vincent, Qiu, Wei, Kermode, Allan G., Lau, Alexander Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426866/
https://www.ncbi.nlm.nih.gov/pubmed/32792656
http://dx.doi.org/10.1038/s41598-020-70693-9
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author Zhao, Lin
Abrigo, Jill
Chen, Qianyun
Au, Cheryl
Ng, Angel
Fan, Ping
Mok, Vincent
Qiu, Wei
Kermode, Allan G.
Lau, Alexander Y.
author_facet Zhao, Lin
Abrigo, Jill
Chen, Qianyun
Au, Cheryl
Ng, Angel
Fan, Ping
Mok, Vincent
Qiu, Wei
Kermode, Allan G.
Lau, Alexander Y.
author_sort Zhao, Lin
collection PubMed
description Oligoclonal IgG bands (OCB) in cerebrospinal fluid (CSF) are important in diagnosis of multiple sclerosis (MS). We evaluated the MRI features of clinically definite MS subjects with and without CSF-OCB. Relapsing MS subjects were recruited from a prospective registry in a university center. CSF-OCB were detected using isoelectric focusing and lgG-specific immunofixation. MRI metrics including brain volumes, lesion volumes and microstructural measures, were analyzed by FMRIB Software Library (FSL) and Statistical Parametric Mapping (SPM). Seventy-five subjects with relapsing MS were analyzed. Forty-four (59%) subjects had an interval MRI at around 1 year. CSF-OCB were detected in 46 (61%) subjects. The OCB-positive group had a higher proportion of cerebellar lesions than the OCB-negative group (23.9% vs. 3.4%, p = 0.057). Except for amygdala volumes which were lower in the OCB-positive group (p = 0.034), other regional brain volumes including the subcortical deep gray matter and corpus callosum were similar. The two groups also showed comparable brain atrophy rate. For DTI, the OCB-positive group showed significantly higher mean diffusivity (MD) value in perilesional normal-appearing white matter (p = 0.043). Relapsing MS patients with and without CSF-OCB shared similar MRI features regarding volumetric analyses and DTI microstructural integrity.
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spelling pubmed-74268662020-08-14 Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands Zhao, Lin Abrigo, Jill Chen, Qianyun Au, Cheryl Ng, Angel Fan, Ping Mok, Vincent Qiu, Wei Kermode, Allan G. Lau, Alexander Y. Sci Rep Article Oligoclonal IgG bands (OCB) in cerebrospinal fluid (CSF) are important in diagnosis of multiple sclerosis (MS). We evaluated the MRI features of clinically definite MS subjects with and without CSF-OCB. Relapsing MS subjects were recruited from a prospective registry in a university center. CSF-OCB were detected using isoelectric focusing and lgG-specific immunofixation. MRI metrics including brain volumes, lesion volumes and microstructural measures, were analyzed by FMRIB Software Library (FSL) and Statistical Parametric Mapping (SPM). Seventy-five subjects with relapsing MS were analyzed. Forty-four (59%) subjects had an interval MRI at around 1 year. CSF-OCB were detected in 46 (61%) subjects. The OCB-positive group had a higher proportion of cerebellar lesions than the OCB-negative group (23.9% vs. 3.4%, p = 0.057). Except for amygdala volumes which were lower in the OCB-positive group (p = 0.034), other regional brain volumes including the subcortical deep gray matter and corpus callosum were similar. The two groups also showed comparable brain atrophy rate. For DTI, the OCB-positive group showed significantly higher mean diffusivity (MD) value in perilesional normal-appearing white matter (p = 0.043). Relapsing MS patients with and without CSF-OCB shared similar MRI features regarding volumetric analyses and DTI microstructural integrity. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426866/ /pubmed/32792656 http://dx.doi.org/10.1038/s41598-020-70693-9 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhao, Lin
Abrigo, Jill
Chen, Qianyun
Au, Cheryl
Ng, Angel
Fan, Ping
Mok, Vincent
Qiu, Wei
Kermode, Allan G.
Lau, Alexander Y.
Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands
title Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands
title_full Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands
title_fullStr Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands
title_full_unstemmed Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands
title_short Advanced MRI features in relapsing multiple sclerosis patients with and without CSF oligoclonal IgG bands
title_sort advanced mri features in relapsing multiple sclerosis patients with and without csf oligoclonal igg bands
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426866/
https://www.ncbi.nlm.nih.gov/pubmed/32792656
http://dx.doi.org/10.1038/s41598-020-70693-9
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