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Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers

BACKGROUND: Results from recent clinical studies suggest that cerebrospinal fluid (CSF) biomarkers that are indicative of Alzheimer’s disease (AD) can be replicated in blood, e.g. amyloid-beta peptides (Aβ(42) and Aβ(40)) and neurofilament light chain (NFL). Such data proposes that blood is a rich s...

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Autores principales: Ashton, Nicholas J., Suárez-Calvet, Marc, Heslegrave, Amanda, Hye, Abdul, Razquin, Cristina, Pastor, Pau, Sanchez-Valle, Raquel, Molinuevo, José L., Visser, Pieter Jelle, Blennow, Kaj, Hodges, Angela K., Zetterberg, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883551/
https://www.ncbi.nlm.nih.gov/pubmed/31779670
http://dx.doi.org/10.1186/s13195-019-0545-5
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author Ashton, Nicholas J.
Suárez-Calvet, Marc
Heslegrave, Amanda
Hye, Abdul
Razquin, Cristina
Pastor, Pau
Sanchez-Valle, Raquel
Molinuevo, José L.
Visser, Pieter Jelle
Blennow, Kaj
Hodges, Angela K.
Zetterberg, Henrik
author_facet Ashton, Nicholas J.
Suárez-Calvet, Marc
Heslegrave, Amanda
Hye, Abdul
Razquin, Cristina
Pastor, Pau
Sanchez-Valle, Raquel
Molinuevo, José L.
Visser, Pieter Jelle
Blennow, Kaj
Hodges, Angela K.
Zetterberg, Henrik
author_sort Ashton, Nicholas J.
collection PubMed
description BACKGROUND: Results from recent clinical studies suggest that cerebrospinal fluid (CSF) biomarkers that are indicative of Alzheimer’s disease (AD) can be replicated in blood, e.g. amyloid-beta peptides (Aβ(42) and Aβ(40)) and neurofilament light chain (NFL). Such data proposes that blood is a rich source of potential biomarkers reflecting central nervous system pathophysiology and should be fully explored for biomarkers that show promise in CSF. Recently, soluble fragments of the triggering receptor expressed on myeloid cells 2 (sTREM2) protein in CSF have been reported to be increased in prodromal AD and also in individuals with TREM2 rare genetic variants that increase the likelihood of developing dementia. METHODS: In this study, we measured the levels of plasma sTREM2 and plasma NFL using the MesoScale Discovery and single molecule array platforms, respectively, in 48 confirmed TREM2 rare variant carriers and 49 non-carriers. RESULTS: Our results indicate that there are no changes in plasma sTREM2 and NFL concentrations between TREM2 rare variant carriers and non-carriers. Furthermore, plasma sTREM2 is not different between healthy controls, mild cognitive impairment (MCI) or AD. CONCLUSION: Concentrations of plasma sTREM2 do not mimic the recent changes found in CSF sTREM2.
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spelling pubmed-68835512019-12-03 Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers Ashton, Nicholas J. Suárez-Calvet, Marc Heslegrave, Amanda Hye, Abdul Razquin, Cristina Pastor, Pau Sanchez-Valle, Raquel Molinuevo, José L. Visser, Pieter Jelle Blennow, Kaj Hodges, Angela K. Zetterberg, Henrik Alzheimers Res Ther Research BACKGROUND: Results from recent clinical studies suggest that cerebrospinal fluid (CSF) biomarkers that are indicative of Alzheimer’s disease (AD) can be replicated in blood, e.g. amyloid-beta peptides (Aβ(42) and Aβ(40)) and neurofilament light chain (NFL). Such data proposes that blood is a rich source of potential biomarkers reflecting central nervous system pathophysiology and should be fully explored for biomarkers that show promise in CSF. Recently, soluble fragments of the triggering receptor expressed on myeloid cells 2 (sTREM2) protein in CSF have been reported to be increased in prodromal AD and also in individuals with TREM2 rare genetic variants that increase the likelihood of developing dementia. METHODS: In this study, we measured the levels of plasma sTREM2 and plasma NFL using the MesoScale Discovery and single molecule array platforms, respectively, in 48 confirmed TREM2 rare variant carriers and 49 non-carriers. RESULTS: Our results indicate that there are no changes in plasma sTREM2 and NFL concentrations between TREM2 rare variant carriers and non-carriers. Furthermore, plasma sTREM2 is not different between healthy controls, mild cognitive impairment (MCI) or AD. CONCLUSION: Concentrations of plasma sTREM2 do not mimic the recent changes found in CSF sTREM2. BioMed Central 2019-11-28 /pmc/articles/PMC6883551/ /pubmed/31779670 http://dx.doi.org/10.1186/s13195-019-0545-5 Text en © The Author(s). 2019 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
Ashton, Nicholas J.
Suárez-Calvet, Marc
Heslegrave, Amanda
Hye, Abdul
Razquin, Cristina
Pastor, Pau
Sanchez-Valle, Raquel
Molinuevo, José L.
Visser, Pieter Jelle
Blennow, Kaj
Hodges, Angela K.
Zetterberg, Henrik
Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers
title Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers
title_full Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers
title_fullStr Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers
title_full_unstemmed Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers
title_short Plasma levels of soluble TREM2 and neurofilament light chain in TREM2 rare variant carriers
title_sort plasma levels of soluble trem2 and neurofilament light chain in trem2 rare variant carriers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883551/
https://www.ncbi.nlm.nih.gov/pubmed/31779670
http://dx.doi.org/10.1186/s13195-019-0545-5
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