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Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study

BACKGROUND: Neurofilament light (NFL) has been increasingly recognized for prognostic and therapeutic decisions. OBJECTIVE: To validate the utility of cerebrospinal fluid NFL (cNFL) as a biomarker in clinical practice of relapsing-remitting multiple sclerosis (RRMS). METHODS: RRMS patients (n = 757)...

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Autores principales: Rosenstein, Igal, Axelsson, Markus, Novakova, Lenka, Blennow, Kaj, Zetterberg, Henrik, Lycke, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024026/
https://www.ncbi.nlm.nih.gov/pubmed/34392718
http://dx.doi.org/10.1177/13524585211039104
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author Rosenstein, Igal
Axelsson, Markus
Novakova, Lenka
Blennow, Kaj
Zetterberg, Henrik
Lycke, Jan
author_facet Rosenstein, Igal
Axelsson, Markus
Novakova, Lenka
Blennow, Kaj
Zetterberg, Henrik
Lycke, Jan
author_sort Rosenstein, Igal
collection PubMed
description BACKGROUND: Neurofilament light (NFL) has been increasingly recognized for prognostic and therapeutic decisions. OBJECTIVE: To validate the utility of cerebrospinal fluid NFL (cNFL) as a biomarker in clinical practice of relapsing-remitting multiple sclerosis (RRMS). METHODS: RRMS patients (n = 757) who had cNFL analyzed as part of the diagnostic work-up in a single academic multiple sclerosis (MS) center, 2001–2018, were retrospectively identified. cNFL concentrations were determined with two different immunoassays and the ratio of means between them was used for normalization. RESULTS: RRMS with relapse had 4.4 times higher median cNFL concentration (1134 [interquartile range (IQR) 499–2744] ng/L) than those without relapse (264 [125–537] ng/L, p < 0.001) and patients with gadolinium-enhancing lesions had 3.3 times higher median NFL (1414 [606.8–3210] ng/L) than those without (426 [IQR 221–851] ng/L, p < 0.001). The sensitivity and specificity of cNFL to detect disease activity was 75% and 98.5%, respectively. High cNFL at MS onset predicted progression to Expanded Disability Status Scale (EDSS) ⩾ 3 (p < 0.001, hazard ratios (HR) = 1.89, 95% CI = 1.44–2.65) and conversion to secondary progressive MS (SPMS, p = 0.001, HR = 2.5, 95% CI = 1.4–4.2). CONCLUSIONS: cNFL is a robust and reliable biomarker of disease activity, treatment response, and prediction of disability and conversion from RRMS to SPMS. Our data suggest that cNFL should be included in the assessment of patients at MS-onset.
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spelling pubmed-90240262022-04-23 Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study Rosenstein, Igal Axelsson, Markus Novakova, Lenka Blennow, Kaj Zetterberg, Henrik Lycke, Jan Mult Scler Original Research Papers BACKGROUND: Neurofilament light (NFL) has been increasingly recognized for prognostic and therapeutic decisions. OBJECTIVE: To validate the utility of cerebrospinal fluid NFL (cNFL) as a biomarker in clinical practice of relapsing-remitting multiple sclerosis (RRMS). METHODS: RRMS patients (n = 757) who had cNFL analyzed as part of the diagnostic work-up in a single academic multiple sclerosis (MS) center, 2001–2018, were retrospectively identified. cNFL concentrations were determined with two different immunoassays and the ratio of means between them was used for normalization. RESULTS: RRMS with relapse had 4.4 times higher median cNFL concentration (1134 [interquartile range (IQR) 499–2744] ng/L) than those without relapse (264 [125–537] ng/L, p < 0.001) and patients with gadolinium-enhancing lesions had 3.3 times higher median NFL (1414 [606.8–3210] ng/L) than those without (426 [IQR 221–851] ng/L, p < 0.001). The sensitivity and specificity of cNFL to detect disease activity was 75% and 98.5%, respectively. High cNFL at MS onset predicted progression to Expanded Disability Status Scale (EDSS) ⩾ 3 (p < 0.001, hazard ratios (HR) = 1.89, 95% CI = 1.44–2.65) and conversion to secondary progressive MS (SPMS, p = 0.001, HR = 2.5, 95% CI = 1.4–4.2). CONCLUSIONS: cNFL is a robust and reliable biomarker of disease activity, treatment response, and prediction of disability and conversion from RRMS to SPMS. Our data suggest that cNFL should be included in the assessment of patients at MS-onset. SAGE Publications 2021-08-16 2022-05 /pmc/articles/PMC9024026/ /pubmed/34392718 http://dx.doi.org/10.1177/13524585211039104 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Papers
Rosenstein, Igal
Axelsson, Markus
Novakova, Lenka
Blennow, Kaj
Zetterberg, Henrik
Lycke, Jan
Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study
title Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study
title_full Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study
title_fullStr Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study
title_full_unstemmed Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study
title_short Exploring CSF neurofilament light as a biomarker for MS in clinical practice; a retrospective registry-based study
title_sort exploring csf neurofilament light as a biomarker for ms in clinical practice; a retrospective registry-based study
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024026/
https://www.ncbi.nlm.nih.gov/pubmed/34392718
http://dx.doi.org/10.1177/13524585211039104
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