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CSF parameters associated with early MRI activity in patients with MS
OBJECTIVE: To identify CSF parameters at diagnosis of clinically isolated syndrome (CIS) and MS that are associated with early inflammatory disease activity as measured by standardized cerebral MRI (cMRI). METHODS: One hundred forty-nine patients with newly diagnosed CIS and MS were included in the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624100/ https://www.ncbi.nlm.nih.gov/pubmed/31355309 http://dx.doi.org/10.1212/NXI.0000000000000573 |
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author | Klein, Ana Selter, Rebecca C. Hapfelmeier, Alexander Berthele, Achim Müller-Myhsok, Bertram Pongratz, Viola Gasperi, Christiane Zimmer, Claus Mühlau, Mark Hemmer, Bernhard |
author_facet | Klein, Ana Selter, Rebecca C. Hapfelmeier, Alexander Berthele, Achim Müller-Myhsok, Bertram Pongratz, Viola Gasperi, Christiane Zimmer, Claus Mühlau, Mark Hemmer, Bernhard |
author_sort | Klein, Ana |
collection | PubMed |
description | OBJECTIVE: To identify CSF parameters at diagnosis of clinically isolated syndrome (CIS) and MS that are associated with early inflammatory disease activity as measured by standardized cerebral MRI (cMRI). METHODS: One hundred forty-nine patients with newly diagnosed CIS and MS were included in the retrospective study. cMRI at onset and after 12 months was analyzed for T2 and gadolinium-enhancing lesions. CSF was tested for oligoclonal bands and intrathecal synthesis of immunoglobulin G (IgG), A (IgA), and M (IgM) before initiation of disease-modifying therapy (DMT). In a subgroup of patients, CSF and serum samples were analyzed for sCD27, neurofilament light chain, and IgG subclasses 1 and 3. Association between CSF parameters and cMRI activity was investigated by univariable and multivariable regression analysis in all patients, DMT-treated patients, and untreated patients. RESULTS: IgG index, sCD27 levels in CSF, and to a lesser extent IgM index were associated with the occurrence of new cMRI lesions. IgG index and sCD27 levels in CSF were highly correlated. In a multivariable analysis, IgG index and to a lesser extent IgM index together with DMT treatment status and gender were strongest predictors of future cMRI activity. CONCLUSIONS: CSF parameters such as IgG and IgM index are independently associated with future MRI activity and thus might be helpful to support early treatment decisions in patients newly diagnosed with CIS and MS. |
format | Online Article Text |
id | pubmed-6624100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-66241002019-07-26 CSF parameters associated with early MRI activity in patients with MS Klein, Ana Selter, Rebecca C. Hapfelmeier, Alexander Berthele, Achim Müller-Myhsok, Bertram Pongratz, Viola Gasperi, Christiane Zimmer, Claus Mühlau, Mark Hemmer, Bernhard Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To identify CSF parameters at diagnosis of clinically isolated syndrome (CIS) and MS that are associated with early inflammatory disease activity as measured by standardized cerebral MRI (cMRI). METHODS: One hundred forty-nine patients with newly diagnosed CIS and MS were included in the retrospective study. cMRI at onset and after 12 months was analyzed for T2 and gadolinium-enhancing lesions. CSF was tested for oligoclonal bands and intrathecal synthesis of immunoglobulin G (IgG), A (IgA), and M (IgM) before initiation of disease-modifying therapy (DMT). In a subgroup of patients, CSF and serum samples were analyzed for sCD27, neurofilament light chain, and IgG subclasses 1 and 3. Association between CSF parameters and cMRI activity was investigated by univariable and multivariable regression analysis in all patients, DMT-treated patients, and untreated patients. RESULTS: IgG index, sCD27 levels in CSF, and to a lesser extent IgM index were associated with the occurrence of new cMRI lesions. IgG index and sCD27 levels in CSF were highly correlated. In a multivariable analysis, IgG index and to a lesser extent IgM index together with DMT treatment status and gender were strongest predictors of future cMRI activity. CONCLUSIONS: CSF parameters such as IgG and IgM index are independently associated with future MRI activity and thus might be helpful to support early treatment decisions in patients newly diagnosed with CIS and MS. Lippincott Williams & Wilkins 2019-05-30 /pmc/articles/PMC6624100/ /pubmed/31355309 http://dx.doi.org/10.1212/NXI.0000000000000573 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Klein, Ana Selter, Rebecca C. Hapfelmeier, Alexander Berthele, Achim Müller-Myhsok, Bertram Pongratz, Viola Gasperi, Christiane Zimmer, Claus Mühlau, Mark Hemmer, Bernhard CSF parameters associated with early MRI activity in patients with MS |
title | CSF parameters associated with early MRI activity in patients with MS |
title_full | CSF parameters associated with early MRI activity in patients with MS |
title_fullStr | CSF parameters associated with early MRI activity in patients with MS |
title_full_unstemmed | CSF parameters associated with early MRI activity in patients with MS |
title_short | CSF parameters associated with early MRI activity in patients with MS |
title_sort | csf parameters associated with early mri activity in patients with ms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624100/ https://www.ncbi.nlm.nih.gov/pubmed/31355309 http://dx.doi.org/10.1212/NXI.0000000000000573 |
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