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Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease

BACKGROUND: A growing body of evidence suggests that the plasma concentration of the neurofilament light chain (NfL) might be considered a plasma biomarker for the screening of neurodegeneration in Alzheimer’s disease (AD). METHODS: With a single molecule array method (Simoa, Quanterix), plasma NfL...

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Autores principales: Lewczuk, Piotr, Ermann, Natalia, Andreasson, Ulf, Schultheis, Christian, Podhorna, Jana, Spitzer, Philipp, Maler, Juan Manuel, Kornhuber, Johannes, Blennow, Kaj, Zetterberg, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6064615/
https://www.ncbi.nlm.nih.gov/pubmed/30055655
http://dx.doi.org/10.1186/s13195-018-0404-9
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author Lewczuk, Piotr
Ermann, Natalia
Andreasson, Ulf
Schultheis, Christian
Podhorna, Jana
Spitzer, Philipp
Maler, Juan Manuel
Kornhuber, Johannes
Blennow, Kaj
Zetterberg, Henrik
author_facet Lewczuk, Piotr
Ermann, Natalia
Andreasson, Ulf
Schultheis, Christian
Podhorna, Jana
Spitzer, Philipp
Maler, Juan Manuel
Kornhuber, Johannes
Blennow, Kaj
Zetterberg, Henrik
author_sort Lewczuk, Piotr
collection PubMed
description BACKGROUND: A growing body of evidence suggests that the plasma concentration of the neurofilament light chain (NfL) might be considered a plasma biomarker for the screening of neurodegeneration in Alzheimer’s disease (AD). METHODS: With a single molecule array method (Simoa, Quanterix), plasma NfL concentrations were measured in 99 subjects with AD at the stage of mild cognitive impairment (MCI-AD; n = 25) or at the stage of early dementia (ADD; n = 33), and in nondemented controls (n = 41); in all patients, the clinical diagnoses were in accordance with the results of the four core cerebrospinal fluid (CSF) biomarkers (amyloid β (Aβ)1–42, Aβ42/40, Tau, and pTau181), interpreted according to the Erlangen Score algorithm. The influence of preanalytical storage procedures on the NfL in plasma was tested on samples exposed to six different conditions. RESULTS: NfL concentrations significantly increased in the samples exposed to more than one freezing/thawing cycle, and in those stored for 5 days at room temperature or at 4 °C. Compared with the control group of nondemented subjects (22.0 ± 12.4 pg/mL), the unadjusted plasma NfL concentration was highly significantly higher in the MCI-AD group (38.1 ± 15.9 pg/mL, p < 0.005) and even further elevated in the ADD group (49.1 ± 28.4 pg/mL; p < 0.001). A significant association between NfL and age (ρ = 0.65, p < 0.001) was observed; after correcting for age, the difference in NfL concentrations between AD and controls remained significant (p = 0.044). At the cutoff value of 25.7 pg/mL, unconditional sensitivity, specificity, and accuracy were 0.84, 0.78, and 0.82, respectively. Unadjusted correlation between plasma NfL and Mini Mental State Examination (MMSE) across all patients was moderate but significant (r = −0.49, p < 0.001). We observed an overall significant correlation between plasma NfL and the CSF biomarkers, but this correlation was not observed within the diagnostic groups. CONCLUSIONS: This study confirms increased concentrations of plasma NfL in patients with Alzheimer’s disease compared with nondemented controls.
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spelling pubmed-60646152018-08-01 Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease Lewczuk, Piotr Ermann, Natalia Andreasson, Ulf Schultheis, Christian Podhorna, Jana Spitzer, Philipp Maler, Juan Manuel Kornhuber, Johannes Blennow, Kaj Zetterberg, Henrik Alzheimers Res Ther Research BACKGROUND: A growing body of evidence suggests that the plasma concentration of the neurofilament light chain (NfL) might be considered a plasma biomarker for the screening of neurodegeneration in Alzheimer’s disease (AD). METHODS: With a single molecule array method (Simoa, Quanterix), plasma NfL concentrations were measured in 99 subjects with AD at the stage of mild cognitive impairment (MCI-AD; n = 25) or at the stage of early dementia (ADD; n = 33), and in nondemented controls (n = 41); in all patients, the clinical diagnoses were in accordance with the results of the four core cerebrospinal fluid (CSF) biomarkers (amyloid β (Aβ)1–42, Aβ42/40, Tau, and pTau181), interpreted according to the Erlangen Score algorithm. The influence of preanalytical storage procedures on the NfL in plasma was tested on samples exposed to six different conditions. RESULTS: NfL concentrations significantly increased in the samples exposed to more than one freezing/thawing cycle, and in those stored for 5 days at room temperature or at 4 °C. Compared with the control group of nondemented subjects (22.0 ± 12.4 pg/mL), the unadjusted plasma NfL concentration was highly significantly higher in the MCI-AD group (38.1 ± 15.9 pg/mL, p < 0.005) and even further elevated in the ADD group (49.1 ± 28.4 pg/mL; p < 0.001). A significant association between NfL and age (ρ = 0.65, p < 0.001) was observed; after correcting for age, the difference in NfL concentrations between AD and controls remained significant (p = 0.044). At the cutoff value of 25.7 pg/mL, unconditional sensitivity, specificity, and accuracy were 0.84, 0.78, and 0.82, respectively. Unadjusted correlation between plasma NfL and Mini Mental State Examination (MMSE) across all patients was moderate but significant (r = −0.49, p < 0.001). We observed an overall significant correlation between plasma NfL and the CSF biomarkers, but this correlation was not observed within the diagnostic groups. CONCLUSIONS: This study confirms increased concentrations of plasma NfL in patients with Alzheimer’s disease compared with nondemented controls. BioMed Central 2018-07-28 /pmc/articles/PMC6064615/ /pubmed/30055655 http://dx.doi.org/10.1186/s13195-018-0404-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lewczuk, Piotr
Ermann, Natalia
Andreasson, Ulf
Schultheis, Christian
Podhorna, Jana
Spitzer, Philipp
Maler, Juan Manuel
Kornhuber, Johannes
Blennow, Kaj
Zetterberg, Henrik
Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease
title Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease
title_full Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease
title_fullStr Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease
title_full_unstemmed Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease
title_short Plasma neurofilament light as a potential biomarker of neurodegeneration in Alzheimer’s disease
title_sort plasma neurofilament light as a potential biomarker of neurodegeneration in alzheimer’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6064615/
https://www.ncbi.nlm.nih.gov/pubmed/30055655
http://dx.doi.org/10.1186/s13195-018-0404-9
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