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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6816316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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