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A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study

BACKGROUND: Neurofilament light in serum (sNfL) is a biomarker for axonal damage with elevated levels in many neurological disorders, including neurodegenerative dementias. Since within-group variation of sNfL is large and concentrations increase with aging, sNfL’s clinical use in memory clinic prac...

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Autores principales: Willemse, E. A. J., Scheltens, P., Teunissen, C. E., Vijverberg, E. G. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132439/
https://www.ncbi.nlm.nih.gov/pubmed/34006321
http://dx.doi.org/10.1186/s13195-021-00841-4
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author Willemse, E. A. J.
Scheltens, P.
Teunissen, C. E.
Vijverberg, E. G. B.
author_facet Willemse, E. A. J.
Scheltens, P.
Teunissen, C. E.
Vijverberg, E. G. B.
author_sort Willemse, E. A. J.
collection PubMed
description BACKGROUND: Neurofilament light in serum (sNfL) is a biomarker for axonal damage with elevated levels in many neurological disorders, including neurodegenerative dementias. Since within-group variation of sNfL is large and concentrations increase with aging, sNfL’s clinical use in memory clinic practice remains to be established. The objective of the current study was to evaluate the clinical use of serum neurofilament light (sNfL), a cross-disease biomarker for axonal damage, in a tertiary memory clinic cohort. METHODS: Six neurologists completed questionnaires regarding the usefulness of sNfL (n = 5–42 questionnaires/neurologist). Patients that visited the Alzheimer Center Amsterdam for the first time between May and October 2019 (n = 109) were prospectively included in this single-center implementation study. SNfL levels were analyzed on Simoa and reported together with normal values in relation to age, as part of routine diagnostic work-up and in addition to cerebrospinal fluid (CSF) biomarker analysis. RESULTS: SNfL was perceived as useful in 53% (n = 58) of the cases. SNfL was more often perceived as useful in patients < 62 years (29/48, 60%, p = 0.05) and males (41/65, 63%, p < 0.01). Availability of CSF biomarker results at time of result discussion had no influence. We observed non-significant trends for increased perceived usefulness of sNfL for patients with the diagnosis subjective cognitive decline (64%), psychiatric disorder (71%), or uncertain diagnosis (67%). SNfL was mostly helpful to neurologists in confirming or excluding neurodegeneration. Whether sNfL was regarded as useful strongly depended on which neurologist filled out the questionnaire (ranging from 0 to 73% of useful cases/neurologist). DISCUSSION: Regardless of the availability of CSF biomarker results, sNfL was perceived as a useful tool in more than half of the evaluated cases in a tertiary memory clinic practice. Based on our results, we recommend the analysis of the biomarker sNfL to confirm or exclude neurodegeneration in patients below 62 years old and in males. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-021-00841-4.
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spelling pubmed-81324392021-05-19 A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study Willemse, E. A. J. Scheltens, P. Teunissen, C. E. Vijverberg, E. G. B. Alzheimers Res Ther Research BACKGROUND: Neurofilament light in serum (sNfL) is a biomarker for axonal damage with elevated levels in many neurological disorders, including neurodegenerative dementias. Since within-group variation of sNfL is large and concentrations increase with aging, sNfL’s clinical use in memory clinic practice remains to be established. The objective of the current study was to evaluate the clinical use of serum neurofilament light (sNfL), a cross-disease biomarker for axonal damage, in a tertiary memory clinic cohort. METHODS: Six neurologists completed questionnaires regarding the usefulness of sNfL (n = 5–42 questionnaires/neurologist). Patients that visited the Alzheimer Center Amsterdam for the first time between May and October 2019 (n = 109) were prospectively included in this single-center implementation study. SNfL levels were analyzed on Simoa and reported together with normal values in relation to age, as part of routine diagnostic work-up and in addition to cerebrospinal fluid (CSF) biomarker analysis. RESULTS: SNfL was perceived as useful in 53% (n = 58) of the cases. SNfL was more often perceived as useful in patients < 62 years (29/48, 60%, p = 0.05) and males (41/65, 63%, p < 0.01). Availability of CSF biomarker results at time of result discussion had no influence. We observed non-significant trends for increased perceived usefulness of sNfL for patients with the diagnosis subjective cognitive decline (64%), psychiatric disorder (71%), or uncertain diagnosis (67%). SNfL was mostly helpful to neurologists in confirming or excluding neurodegeneration. Whether sNfL was regarded as useful strongly depended on which neurologist filled out the questionnaire (ranging from 0 to 73% of useful cases/neurologist). DISCUSSION: Regardless of the availability of CSF biomarker results, sNfL was perceived as a useful tool in more than half of the evaluated cases in a tertiary memory clinic practice. Based on our results, we recommend the analysis of the biomarker sNfL to confirm or exclude neurodegeneration in patients below 62 years old and in males. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-021-00841-4. BioMed Central 2021-05-18 /pmc/articles/PMC8132439/ /pubmed/34006321 http://dx.doi.org/10.1186/s13195-021-00841-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Willemse, E. A. J.
Scheltens, P.
Teunissen, C. E.
Vijverberg, E. G. B.
A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
title A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
title_full A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
title_fullStr A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
title_full_unstemmed A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
title_short A neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
title_sort neurologist’s perspective on serum neurofilament light in the memory clinic: a prospective implementation study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132439/
https://www.ncbi.nlm.nih.gov/pubmed/34006321
http://dx.doi.org/10.1186/s13195-021-00841-4
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