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High serum neurofilament associates with diffuse white matter damage in MS

OBJECTIVE: To evaluate to which extent serum neurofilament light chain (NfL) increase is related to diffusion tensor imaging–MRI measurable diffuse normal-appearing white matter (NAWM) damage in MS. METHODS: Seventy-nine patients with MS and 10 healthy controls underwent MRI including diffusion tens...

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Autores principales: Saraste, Maija, Bezukladova, Svetlana, Matilainen, Markus, Tuisku, Jouni, Rissanen, Eero, Sucksdorff, Marcus, Laaksonen, Sini, Vuorimaa, Anna, Kuhle, Jens, Leppert, David, Airas, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803327/
https://www.ncbi.nlm.nih.gov/pubmed/33293460
http://dx.doi.org/10.1212/NXI.0000000000000926
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author Saraste, Maija
Bezukladova, Svetlana
Matilainen, Markus
Tuisku, Jouni
Rissanen, Eero
Sucksdorff, Marcus
Laaksonen, Sini
Vuorimaa, Anna
Kuhle, Jens
Leppert, David
Airas, Laura
author_facet Saraste, Maija
Bezukladova, Svetlana
Matilainen, Markus
Tuisku, Jouni
Rissanen, Eero
Sucksdorff, Marcus
Laaksonen, Sini
Vuorimaa, Anna
Kuhle, Jens
Leppert, David
Airas, Laura
author_sort Saraste, Maija
collection PubMed
description OBJECTIVE: To evaluate to which extent serum neurofilament light chain (NfL) increase is related to diffusion tensor imaging–MRI measurable diffuse normal-appearing white matter (NAWM) damage in MS. METHODS: Seventy-nine patients with MS and 10 healthy controls underwent MRI including diffusion tensor sequences and serum NfL determination by single molecule array (Simoa). Fractional anisotropy and mean, axial, and radial diffusivities were calculated within the whole and segmented (frontal, parietal, temporal, occipital, cingulate, and deep) NAWM. Spearman correlations and multiple regression models were used to assess the associations between diffusion tensor imaging, volumetric MRI data, and NfL. RESULTS: Elevated NfL correlated with decreased fractional anisotropy and increased mean, axial, and radial diffusivities in the entire and segmented NAWM (for entire NAWM ρ = −0.49, p = 0.005; ρ = 0.49, p = 0.005; ρ = 0.43, p = 0.018; and ρ = 0.48, p = 0.006, respectively). A multiple regression model examining the effect of diffusion tensor indices on NfL showed significant associations when adjusted for sex, age, disease type, the expanded disability status scale, treatment, and presence of relapses. In the same model, T2 lesion volume was similarly associated with NfL. CONCLUSIONS: Our findings suggest that elevated serum NfL in MS results from neuroaxonal damage both within the NAWM and focal T2 lesions. This pathologic heterogeneity ought to be taken into account when interpreting NfL findings at the individual patient level.
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spelling pubmed-78033272021-03-15 High serum neurofilament associates with diffuse white matter damage in MS Saraste, Maija Bezukladova, Svetlana Matilainen, Markus Tuisku, Jouni Rissanen, Eero Sucksdorff, Marcus Laaksonen, Sini Vuorimaa, Anna Kuhle, Jens Leppert, David Airas, Laura Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To evaluate to which extent serum neurofilament light chain (NfL) increase is related to diffusion tensor imaging–MRI measurable diffuse normal-appearing white matter (NAWM) damage in MS. METHODS: Seventy-nine patients with MS and 10 healthy controls underwent MRI including diffusion tensor sequences and serum NfL determination by single molecule array (Simoa). Fractional anisotropy and mean, axial, and radial diffusivities were calculated within the whole and segmented (frontal, parietal, temporal, occipital, cingulate, and deep) NAWM. Spearman correlations and multiple regression models were used to assess the associations between diffusion tensor imaging, volumetric MRI data, and NfL. RESULTS: Elevated NfL correlated with decreased fractional anisotropy and increased mean, axial, and radial diffusivities in the entire and segmented NAWM (for entire NAWM ρ = −0.49, p = 0.005; ρ = 0.49, p = 0.005; ρ = 0.43, p = 0.018; and ρ = 0.48, p = 0.006, respectively). A multiple regression model examining the effect of diffusion tensor indices on NfL showed significant associations when adjusted for sex, age, disease type, the expanded disability status scale, treatment, and presence of relapses. In the same model, T2 lesion volume was similarly associated with NfL. CONCLUSIONS: Our findings suggest that elevated serum NfL in MS results from neuroaxonal damage both within the NAWM and focal T2 lesions. This pathologic heterogeneity ought to be taken into account when interpreting NfL findings at the individual patient level. Lippincott Williams & Wilkins 2020-12-08 /pmc/articles/PMC7803327/ /pubmed/33293460 http://dx.doi.org/10.1212/NXI.0000000000000926 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
Saraste, Maija
Bezukladova, Svetlana
Matilainen, Markus
Tuisku, Jouni
Rissanen, Eero
Sucksdorff, Marcus
Laaksonen, Sini
Vuorimaa, Anna
Kuhle, Jens
Leppert, David
Airas, Laura
High serum neurofilament associates with diffuse white matter damage in MS
title High serum neurofilament associates with diffuse white matter damage in MS
title_full High serum neurofilament associates with diffuse white matter damage in MS
title_fullStr High serum neurofilament associates with diffuse white matter damage in MS
title_full_unstemmed High serum neurofilament associates with diffuse white matter damage in MS
title_short High serum neurofilament associates with diffuse white matter damage in MS
title_sort high serum neurofilament associates with diffuse white matter damage in ms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803327/
https://www.ncbi.nlm.nih.gov/pubmed/33293460
http://dx.doi.org/10.1212/NXI.0000000000000926
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