Cargando…

CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls

BACKGROUND: Neurofilament light chain is a marker of axonal damage and is of interest as a biofluid biomarker for PD. The objective of this study was to investigate whether CSF or serum neurofilament contributes to a combination of CSF biomarkers in defining the optimal biomarker panel for discrimin...

Descripción completa

Detalles Bibliográficos
Autores principales: Oosterveld, Linda P., Verberk, Inge M.W., Majbour, Nour K., El‐Agnaf, Omar M., Weinstein, Henry C., Berendse, Henk W., Teunissen, Charlotte E., van de Berg, Wilma D.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027879/
https://www.ncbi.nlm.nih.gov/pubmed/31737952
http://dx.doi.org/10.1002/mds.27897
_version_ 1783498925272989696
author Oosterveld, Linda P.
Verberk, Inge M.W.
Majbour, Nour K.
El‐Agnaf, Omar M.
Weinstein, Henry C.
Berendse, Henk W.
Teunissen, Charlotte E.
van de Berg, Wilma D.J.
author_facet Oosterveld, Linda P.
Verberk, Inge M.W.
Majbour, Nour K.
El‐Agnaf, Omar M.
Weinstein, Henry C.
Berendse, Henk W.
Teunissen, Charlotte E.
van de Berg, Wilma D.J.
author_sort Oosterveld, Linda P.
collection PubMed
description BACKGROUND: Neurofilament light chain is a marker of axonal damage and is of interest as a biofluid biomarker for PD. The objective of this study was to investigate whether CSF or serum neurofilament contributes to a combination of CSF biomarkers in defining the optimal biomarker panel for discriminating PD patients from healthy controls. In addition, we aimed to assess whether CSF and/or serum neurofilament levels are associated with clinical measures of disease severity. METHODS: We measured neurofilament light chain levels in CSF and/or serum of 139 PD patients and 52 age‐matched healthy controls. We used stepwise logistic regression analyses to test whether neurofilament contributes to a biomarker CSF panel including total, oligomeric, and phosphorylated α‐synuclein and Alzheimer's disease biomarkers. Measures of disease severity included disease duration, UPDRS‐III, Hoehn & Yahr stage, and MMSE. RESULTS: After correcting for age, CSF neurofilament levels were 42% higher in PD patients compared with controls (P < 0.01), whereas serum neurofilament levels were 37% higher (P = 0.08). Combining CSF neurofilament, phosphorylated‐/total α‐synuclein, and oligomeric‐/total α‐synuclein yielded the best‐fitting model for discriminating PD patients from controls (area under the curve 0.92). The discriminatory potential of serum neurofilament in the CSF biomarker panel was similar (area under the curve 0.90). Higher serum neurofilament was associated with a lower MMSE score. There were no other associations between CSF and/or serum neurofilament levels and clinical disease severity. CONCLUSIONS: CSF neurofilament contributes to a panel of CSF α‐synuclein species in differentiating PD patients from healthy controls. Serum neurofilament may have added value to a biofluid biomarker panel for differentiating PD patients from controls. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
format Online
Article
Text
id pubmed-7027879
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-70278792020-02-24 CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls Oosterveld, Linda P. Verberk, Inge M.W. Majbour, Nour K. El‐Agnaf, Omar M. Weinstein, Henry C. Berendse, Henk W. Teunissen, Charlotte E. van de Berg, Wilma D.J. Mov Disord Research Articles BACKGROUND: Neurofilament light chain is a marker of axonal damage and is of interest as a biofluid biomarker for PD. The objective of this study was to investigate whether CSF or serum neurofilament contributes to a combination of CSF biomarkers in defining the optimal biomarker panel for discriminating PD patients from healthy controls. In addition, we aimed to assess whether CSF and/or serum neurofilament levels are associated with clinical measures of disease severity. METHODS: We measured neurofilament light chain levels in CSF and/or serum of 139 PD patients and 52 age‐matched healthy controls. We used stepwise logistic regression analyses to test whether neurofilament contributes to a biomarker CSF panel including total, oligomeric, and phosphorylated α‐synuclein and Alzheimer's disease biomarkers. Measures of disease severity included disease duration, UPDRS‐III, Hoehn & Yahr stage, and MMSE. RESULTS: After correcting for age, CSF neurofilament levels were 42% higher in PD patients compared with controls (P < 0.01), whereas serum neurofilament levels were 37% higher (P = 0.08). Combining CSF neurofilament, phosphorylated‐/total α‐synuclein, and oligomeric‐/total α‐synuclein yielded the best‐fitting model for discriminating PD patients from controls (area under the curve 0.92). The discriminatory potential of serum neurofilament in the CSF biomarker panel was similar (area under the curve 0.90). Higher serum neurofilament was associated with a lower MMSE score. There were no other associations between CSF and/or serum neurofilament levels and clinical disease severity. CONCLUSIONS: CSF neurofilament contributes to a panel of CSF α‐synuclein species in differentiating PD patients from healthy controls. Serum neurofilament may have added value to a biofluid biomarker panel for differentiating PD patients from controls. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. John Wiley & Sons, Inc. 2019-11-18 2020-02 /pmc/articles/PMC7027879/ /pubmed/31737952 http://dx.doi.org/10.1002/mds.27897 Text en © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Oosterveld, Linda P.
Verberk, Inge M.W.
Majbour, Nour K.
El‐Agnaf, Omar M.
Weinstein, Henry C.
Berendse, Henk W.
Teunissen, Charlotte E.
van de Berg, Wilma D.J.
CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls
title CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls
title_full CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls
title_fullStr CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls
title_full_unstemmed CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls
title_short CSF or serum neurofilament light added to α‐Synuclein panel discriminates Parkinson's from controls
title_sort csf or serum neurofilament light added to α‐synuclein panel discriminates parkinson's from controls
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027879/
https://www.ncbi.nlm.nih.gov/pubmed/31737952
http://dx.doi.org/10.1002/mds.27897
work_keys_str_mv AT oosterveldlindap csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT verberkingemw csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT majbournourk csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT elagnafomarm csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT weinsteinhenryc csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT berendsehenkw csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT teunissencharlottee csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols
AT vandebergwilmadj csforserumneurofilamentlightaddedtoasynucleinpaneldiscriminatesparkinsonsfromcontrols