Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected
Abstract In Alzheimer’s disease (AD), tau phosphorylation in the brain and its subsequent release into cerebrospinal fluid (CSF) and blood is a dynamic process that changes during disease evolution. The main aim of our study was to characterize the pattern of changes in phosphorylated tau (p‐tau) in...
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doaj-fa10944cadf0424c84138b7b13f06a8e2021-08-02T16:02:13ZengWileyEMBO Molecular Medicine1757-46761757-46842020-12-011212n/an/a10.15252/emmm.202012921Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detectedMarc Suárez‐Calvet0Thomas K Karikari1Nicholas J Ashton2Juan Lantero Rodríguez3Marta Milà‐Alomà4Juan Domingo Gispert5Gemma Salvadó6Carolina Minguillon7Karine Fauria8Mahnaz Shekari9Oriol Grau‐Rivera10Eider M Arenaza‐Urquijo11Aleix Sala‐Vila12Gonzalo Sánchez‐Benavides13José Maria González‐de‐Echávarri14Gwendlyn Kollmorgen15Erik Stoops16Eugeen Vanmechelen17Henrik Zetterberg18Kaj Blennow19José Luis Molinuevo20for the ALFA StudyBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainDepartment of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Gothenburg SwedenDepartment of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Gothenburg SwedenDepartment of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Gothenburg SwedenBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainRoche Diagnostics GmbH Penzberg GermanyADx NeuroSciences Ghent BelgiumADx NeuroSciences Ghent BelgiumDepartment of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Gothenburg SwedenDepartment of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Gothenburg SwedenBarcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona SpainAbstract In Alzheimer’s disease (AD), tau phosphorylation in the brain and its subsequent release into cerebrospinal fluid (CSF) and blood is a dynamic process that changes during disease evolution. The main aim of our study was to characterize the pattern of changes in phosphorylated tau (p‐tau) in the preclinical stage of the Alzheimer’s continuum. We measured three novel CSF p‐tau biomarkers, phosphorylated at threonine‐181 and threonine‐217 with an N‐terminal partner antibody and at threonine‐231 with a mid‐region partner antibody. These were compared with an automated mid‐region p‐tau181 assay (Elecsys) as the gold standard p‐tau measure. We demonstrate that these novel p‐tau biomarkers increase more prominently in preclinical Alzheimer, when only subtle changes of amyloid‐β (Aβ) pathology are detected, and can accurately differentiate Aβ‐positive from Aβ‐negative cognitively unimpaired individuals. Moreover, we show that the novel plasma N‐terminal p‐tau181 biomarker is mildly but significantly increased in the preclinical stage. Our results support the idea that early changes in neuronal tau metabolism in preclinical Alzheimer, likely in response to Aβ exposure, can be detected with these novel p‐tau assays.https://doi.org/10.15252/emmm.202012921Alzheimer’s diseasebiomarkercerebrospinal fluidplasmatau |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marc Suárez‐Calvet Thomas K Karikari Nicholas J Ashton Juan Lantero Rodríguez Marta Milà‐Alomà Juan Domingo Gispert Gemma Salvadó Carolina Minguillon Karine Fauria Mahnaz Shekari Oriol Grau‐Rivera Eider M Arenaza‐Urquijo Aleix Sala‐Vila Gonzalo Sánchez‐Benavides José Maria González‐de‐Echávarri Gwendlyn Kollmorgen Erik Stoops Eugeen Vanmechelen Henrik Zetterberg Kaj Blennow José Luis Molinuevo for the ALFA Study |
spellingShingle |
Marc Suárez‐Calvet Thomas K Karikari Nicholas J Ashton Juan Lantero Rodríguez Marta Milà‐Alomà Juan Domingo Gispert Gemma Salvadó Carolina Minguillon Karine Fauria Mahnaz Shekari Oriol Grau‐Rivera Eider M Arenaza‐Urquijo Aleix Sala‐Vila Gonzalo Sánchez‐Benavides José Maria González‐de‐Echávarri Gwendlyn Kollmorgen Erik Stoops Eugeen Vanmechelen Henrik Zetterberg Kaj Blennow José Luis Molinuevo for the ALFA Study Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected EMBO Molecular Medicine Alzheimer’s disease biomarker cerebrospinal fluid plasma tau |
author_facet |
Marc Suárez‐Calvet Thomas K Karikari Nicholas J Ashton Juan Lantero Rodríguez Marta Milà‐Alomà Juan Domingo Gispert Gemma Salvadó Carolina Minguillon Karine Fauria Mahnaz Shekari Oriol Grau‐Rivera Eider M Arenaza‐Urquijo Aleix Sala‐Vila Gonzalo Sánchez‐Benavides José Maria González‐de‐Echávarri Gwendlyn Kollmorgen Erik Stoops Eugeen Vanmechelen Henrik Zetterberg Kaj Blennow José Luis Molinuevo for the ALFA Study |
author_sort |
Marc Suárez‐Calvet |
title |
Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected |
title_short |
Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected |
title_full |
Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected |
title_fullStr |
Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected |
title_full_unstemmed |
Novel tau biomarkers phosphorylated at T181, T217 or T231 rise in the initial stages of the preclinical Alzheimer’s continuum when only subtle changes in Aβ pathology are detected |
title_sort |
novel tau biomarkers phosphorylated at t181, t217 or t231 rise in the initial stages of the preclinical alzheimer’s continuum when only subtle changes in aβ pathology are detected |
publisher |
Wiley |
series |
EMBO Molecular Medicine |
issn |
1757-4676 1757-4684 |
publishDate |
2020-12-01 |
description |
Abstract In Alzheimer’s disease (AD), tau phosphorylation in the brain and its subsequent release into cerebrospinal fluid (CSF) and blood is a dynamic process that changes during disease evolution. The main aim of our study was to characterize the pattern of changes in phosphorylated tau (p‐tau) in the preclinical stage of the Alzheimer’s continuum. We measured three novel CSF p‐tau biomarkers, phosphorylated at threonine‐181 and threonine‐217 with an N‐terminal partner antibody and at threonine‐231 with a mid‐region partner antibody. These were compared with an automated mid‐region p‐tau181 assay (Elecsys) as the gold standard p‐tau measure. We demonstrate that these novel p‐tau biomarkers increase more prominently in preclinical Alzheimer, when only subtle changes of amyloid‐β (Aβ) pathology are detected, and can accurately differentiate Aβ‐positive from Aβ‐negative cognitively unimpaired individuals. Moreover, we show that the novel plasma N‐terminal p‐tau181 biomarker is mildly but significantly increased in the preclinical stage. Our results support the idea that early changes in neuronal tau metabolism in preclinical Alzheimer, likely in response to Aβ exposure, can be detected with these novel p‐tau assays. |
topic |
Alzheimer’s disease biomarker cerebrospinal fluid plasma tau |
url |
https://doi.org/10.15252/emmm.202012921 |
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