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Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals

INTRODUCTION: Neurofilament light chain (NfL) is a promising blood biomarker to detect neurodegeneration in Alzheimer's disease (AD) and other brain disorders. However, there are limited reports of how longitudinal NfL relates to imaging biomarkers. We herein investigated the relationship betwe...

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Autores principales: Benedet, Andréa L., Ashton, Nicholas J., Pascoal, Tharick A., Leuzy, Antoine, Mathotaarachchi, Sulantha, Kang, Min S., Therriault, Joseph, Savard, Melissa, Chamoun, Mira, Schöll, Michael, Zimmer, Eduardo R., Gauthier, Serge, Labbe, Aurélie, Zetterberg, Henrik, Blennow, Kaj, Neto, Pedro R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816316/
https://www.ncbi.nlm.nih.gov/pubmed/31673598
http://dx.doi.org/10.1016/j.dadm.2019.08.002
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author Benedet, Andréa L.
Ashton, Nicholas J.
Pascoal, Tharick A.
Leuzy, Antoine
Mathotaarachchi, Sulantha
Kang, Min S.
Therriault, Joseph
Savard, Melissa
Chamoun, Mira
Schöll, Michael
Zimmer, Eduardo R.
Gauthier, Serge
Labbe, Aurélie
Zetterberg, Henrik
Blennow, Kaj
Neto, Pedro R.
author_facet Benedet, Andréa L.
Ashton, Nicholas J.
Pascoal, Tharick A.
Leuzy, Antoine
Mathotaarachchi, Sulantha
Kang, Min S.
Therriault, Joseph
Savard, Melissa
Chamoun, Mira
Schöll, Michael
Zimmer, Eduardo R.
Gauthier, Serge
Labbe, Aurélie
Zetterberg, Henrik
Blennow, Kaj
Neto, Pedro R.
author_sort Benedet, Andréa L.
collection PubMed
description INTRODUCTION: Neurofilament light chain (NfL) is a promising blood biomarker to detect neurodegeneration in Alzheimer's disease (AD) and other brain disorders. However, there are limited reports of how longitudinal NfL relates to imaging biomarkers. We herein investigated the relationship between blood NfL and brain metabolism in AD. METHODS: Voxelwise regression models tested the cross-sectional association between [(18)F]fluorodeoxyglucose ([(18)F]FDG) and both plasma and cerebrospinal fluid NfL in cognitively impaired and unimpaired subjects. Linear mixed models were also used to test the longitudinal association between NfL and [(18)F]FDG in amyloid positive (Aβ+) and negative (Aβ−) subjects. RESULTS: Higher concentrations of plasma and cerebrospinal fluid NfL were associated with reduced [(18)F]FDG uptake in correspondent brain regions. In Aβ+ participants, NfL associates with hypometabolism in AD-vulnerable regions. Longitudinal changes in the association [(18)F]FDG-NfL were confined to cognitively impaired Aβ+ individuals. DISCUSSION: These findings indicate that plasma NfL is a proxy for neurodegeneration in AD-related regions in Aβ+ subjects.
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spelling pubmed-68163162019-10-31 Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals Benedet, Andréa L. Ashton, Nicholas J. Pascoal, Tharick A. Leuzy, Antoine Mathotaarachchi, Sulantha Kang, Min S. Therriault, Joseph Savard, Melissa Chamoun, Mira Schöll, Michael Zimmer, Eduardo R. Gauthier, Serge Labbe, Aurélie Zetterberg, Henrik Blennow, Kaj Neto, Pedro R. Alzheimers Dement (Amst) Special Section: Blood-Based Biomarkers for Alzheimer's Disease & Related Dementias. (Editor: Henrik Zetterberg) INTRODUCTION: Neurofilament light chain (NfL) is a promising blood biomarker to detect neurodegeneration in Alzheimer's disease (AD) and other brain disorders. However, there are limited reports of how longitudinal NfL relates to imaging biomarkers. We herein investigated the relationship between blood NfL and brain metabolism in AD. METHODS: Voxelwise regression models tested the cross-sectional association between [(18)F]fluorodeoxyglucose ([(18)F]FDG) and both plasma and cerebrospinal fluid NfL in cognitively impaired and unimpaired subjects. Linear mixed models were also used to test the longitudinal association between NfL and [(18)F]FDG in amyloid positive (Aβ+) and negative (Aβ−) subjects. RESULTS: Higher concentrations of plasma and cerebrospinal fluid NfL were associated with reduced [(18)F]FDG uptake in correspondent brain regions. In Aβ+ participants, NfL associates with hypometabolism in AD-vulnerable regions. Longitudinal changes in the association [(18)F]FDG-NfL were confined to cognitively impaired Aβ+ individuals. DISCUSSION: These findings indicate that plasma NfL is a proxy for neurodegeneration in AD-related regions in Aβ+ subjects. Elsevier 2019-09-27 /pmc/articles/PMC6816316/ /pubmed/31673598 http://dx.doi.org/10.1016/j.dadm.2019.08.002 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Special Section: Blood-Based Biomarkers for Alzheimer's Disease & Related Dementias. (Editor: Henrik Zetterberg)
Benedet, Andréa L.
Ashton, Nicholas J.
Pascoal, Tharick A.
Leuzy, Antoine
Mathotaarachchi, Sulantha
Kang, Min S.
Therriault, Joseph
Savard, Melissa
Chamoun, Mira
Schöll, Michael
Zimmer, Eduardo R.
Gauthier, Serge
Labbe, Aurélie
Zetterberg, Henrik
Blennow, Kaj
Neto, Pedro R.
Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals
title Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals
title_full Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals
title_fullStr Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals
title_full_unstemmed Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals
title_short Plasma neurofilament light associates with Alzheimer's disease metabolic decline in amyloid-positive individuals
title_sort plasma neurofilament light associates with alzheimer's disease metabolic decline in amyloid-positive individuals
topic Special Section: Blood-Based Biomarkers for Alzheimer's Disease & Related Dementias. (Editor: Henrik Zetterberg)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816316/
https://www.ncbi.nlm.nih.gov/pubmed/31673598
http://dx.doi.org/10.1016/j.dadm.2019.08.002
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