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Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS

OBJECTIVE: To investigate the association of serum neurofilament light chain (sNfL) levels with CSF parameters in clinically isolated syndrome (CIS) and early relapsing-remitting MS (RRMS), taking into account radiologic and clinical parameters of disease activity. METHODS: Simultaneously collected...

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Autores principales: Engel, Sinah, Steffen, Falk, Uphaus, Timo, Scholz-Kreisel, Peter, Zipp, Frauke, Bittner, Stefan, Luessi, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051198/
https://www.ncbi.nlm.nih.gov/pubmed/32019769
http://dx.doi.org/10.1212/NXI.0000000000000679
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author Engel, Sinah
Steffen, Falk
Uphaus, Timo
Scholz-Kreisel, Peter
Zipp, Frauke
Bittner, Stefan
Luessi, Felix
author_facet Engel, Sinah
Steffen, Falk
Uphaus, Timo
Scholz-Kreisel, Peter
Zipp, Frauke
Bittner, Stefan
Luessi, Felix
author_sort Engel, Sinah
collection PubMed
description OBJECTIVE: To investigate the association of serum neurofilament light chain (sNfL) levels with CSF parameters in clinically isolated syndrome (CIS) and early relapsing-remitting MS (RRMS), taking into account radiologic and clinical parameters of disease activity. METHODS: Simultaneously collected serum and CSF samples of 112 untreated patients newly diagnosed with CIS or RRMS were included in this cross-sectional study. CSF parameters were obtained as part of routine diagnostic tests. sNfL levels of patients and of 62 healthy donors were measured by highly sensitive single molecule array (SiMoA) immunoassay. RESULTS: Patients with RRMS (n = 91, median 10.13 pg/mL, interquartile range [IQR] 6.67–17.77 pg/mL) had higher sNfL levels than healthy donors (n = 62, median 5.25 pg/mL, IQR 4.05–6.81 pg/mL, p < 0.001) and patients with CIS (n = 21, median 5.69 pg/mL, IQR 4.73–9.07 pg/mL, p < 0.001). Patients positive for oligoclonal bands (OCBs) (n = 101, median 9.19 pg/mL, IQR 6.34–16.38 pg/mL) had higher sNfL levels than OCB-negative patients (n = 11, median 5.93 pg/mL, IQR 2.93–8.56 pg/mL, p = 0.001). sNfL levels correlated with CSF immunoglobulin G (IgG) levels (r = 0.317, p = 0.002), IgG ratio (QIgG) (r = 0.344, p < 0.001), and CSF leukocyte count (r = 0.288, p = 0.002). In linear regression modeling, the CSF leukocyte count combined with the number of contrast-enhancing lesions in MRI predicted sNfL levels best. CONCLUSIONS: In active MS, sNfL levels correlate with intrathecal pleocytosis and IgG synthesis, indicating that axonal damage is associated with both acute and chronic CNS-intrinsic inflammation.
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spelling pubmed-70511982020-03-13 Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS Engel, Sinah Steffen, Falk Uphaus, Timo Scholz-Kreisel, Peter Zipp, Frauke Bittner, Stefan Luessi, Felix Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To investigate the association of serum neurofilament light chain (sNfL) levels with CSF parameters in clinically isolated syndrome (CIS) and early relapsing-remitting MS (RRMS), taking into account radiologic and clinical parameters of disease activity. METHODS: Simultaneously collected serum and CSF samples of 112 untreated patients newly diagnosed with CIS or RRMS were included in this cross-sectional study. CSF parameters were obtained as part of routine diagnostic tests. sNfL levels of patients and of 62 healthy donors were measured by highly sensitive single molecule array (SiMoA) immunoassay. RESULTS: Patients with RRMS (n = 91, median 10.13 pg/mL, interquartile range [IQR] 6.67–17.77 pg/mL) had higher sNfL levels than healthy donors (n = 62, median 5.25 pg/mL, IQR 4.05–6.81 pg/mL, p < 0.001) and patients with CIS (n = 21, median 5.69 pg/mL, IQR 4.73–9.07 pg/mL, p < 0.001). Patients positive for oligoclonal bands (OCBs) (n = 101, median 9.19 pg/mL, IQR 6.34–16.38 pg/mL) had higher sNfL levels than OCB-negative patients (n = 11, median 5.93 pg/mL, IQR 2.93–8.56 pg/mL, p = 0.001). sNfL levels correlated with CSF immunoglobulin G (IgG) levels (r = 0.317, p = 0.002), IgG ratio (QIgG) (r = 0.344, p < 0.001), and CSF leukocyte count (r = 0.288, p = 0.002). In linear regression modeling, the CSF leukocyte count combined with the number of contrast-enhancing lesions in MRI predicted sNfL levels best. CONCLUSIONS: In active MS, sNfL levels correlate with intrathecal pleocytosis and IgG synthesis, indicating that axonal damage is associated with both acute and chronic CNS-intrinsic inflammation. Lippincott Williams & Wilkins 2020-02-04 /pmc/articles/PMC7051198/ /pubmed/32019769 http://dx.doi.org/10.1212/NXI.0000000000000679 Text en Copyright © 2020 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
Engel, Sinah
Steffen, Falk
Uphaus, Timo
Scholz-Kreisel, Peter
Zipp, Frauke
Bittner, Stefan
Luessi, Felix
Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS
title Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS
title_full Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS
title_fullStr Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS
title_full_unstemmed Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS
title_short Association of intrathecal pleocytosis and IgG synthesis with axonal damage in early MS
title_sort association of intrathecal pleocytosis and igg synthesis with axonal damage in early ms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051198/
https://www.ncbi.nlm.nih.gov/pubmed/32019769
http://dx.doi.org/10.1212/NXI.0000000000000679
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