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Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals
The availability of blood-based assays detecting Alzheimer’s disease (AD) pathology should greatly accelerate AD therapeutic development and improve clinical care. This is especially true for markers that capture the risk of decline in pre-symptomatic stages of AD, as this would allow one to focus i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695712/ https://www.ncbi.nlm.nih.gov/pubmed/33247134 http://dx.doi.org/10.1038/s41467-020-19543-w |
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author | Chhatwal, Jasmeer P. Schultz, Aaron P. Dang, Yifan Ostaszewski, Beth Liu, Lei Yang, Hyun-Sik Johnson, Keith A. Sperling, Reisa A. Selkoe, Dennis J. |
author_facet | Chhatwal, Jasmeer P. Schultz, Aaron P. Dang, Yifan Ostaszewski, Beth Liu, Lei Yang, Hyun-Sik Johnson, Keith A. Sperling, Reisa A. Selkoe, Dennis J. |
author_sort | Chhatwal, Jasmeer P. |
collection | PubMed |
description | The availability of blood-based assays detecting Alzheimer’s disease (AD) pathology should greatly accelerate AD therapeutic development and improve clinical care. This is especially true for markers that capture the risk of decline in pre-symptomatic stages of AD, as this would allow one to focus interventions on participants maximally at risk and at a stage prior to widespread synapse loss and neurodegeneration. Here we quantify plasma concentrations of an N-terminal fragment of tau (NT1) in a large, well-characterized cohort of clinically normal elderly who were followed longitudinally. Plasma NT1 levels at study entry (when all participants were unimpaired) were highly predictive of future cognitive decline, pathological tau accumulation, neurodegeneration, and transition to a diagnosis of MCI/AD. These predictive effects were particularly strong in participants with even modestly elevated brain β-amyloid burden at study entry, suggesting plasma NT1 levels capture very early cognitive, pathologic and neurodegenerative changes along the AD trajectory. |
format | Online Article Text |
id | pubmed-7695712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76957122020-12-03 Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals Chhatwal, Jasmeer P. Schultz, Aaron P. Dang, Yifan Ostaszewski, Beth Liu, Lei Yang, Hyun-Sik Johnson, Keith A. Sperling, Reisa A. Selkoe, Dennis J. Nat Commun Article The availability of blood-based assays detecting Alzheimer’s disease (AD) pathology should greatly accelerate AD therapeutic development and improve clinical care. This is especially true for markers that capture the risk of decline in pre-symptomatic stages of AD, as this would allow one to focus interventions on participants maximally at risk and at a stage prior to widespread synapse loss and neurodegeneration. Here we quantify plasma concentrations of an N-terminal fragment of tau (NT1) in a large, well-characterized cohort of clinically normal elderly who were followed longitudinally. Plasma NT1 levels at study entry (when all participants were unimpaired) were highly predictive of future cognitive decline, pathological tau accumulation, neurodegeneration, and transition to a diagnosis of MCI/AD. These predictive effects were particularly strong in participants with even modestly elevated brain β-amyloid burden at study entry, suggesting plasma NT1 levels capture very early cognitive, pathologic and neurodegenerative changes along the AD trajectory. Nature Publishing Group UK 2020-11-27 /pmc/articles/PMC7695712/ /pubmed/33247134 http://dx.doi.org/10.1038/s41467-020-19543-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chhatwal, Jasmeer P. Schultz, Aaron P. Dang, Yifan Ostaszewski, Beth Liu, Lei Yang, Hyun-Sik Johnson, Keith A. Sperling, Reisa A. Selkoe, Dennis J. Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
title | Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
title_full | Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
title_fullStr | Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
title_full_unstemmed | Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
title_short | Plasma N-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
title_sort | plasma n-terminal tau fragment levels predict future cognitive decline and neurodegeneration in healthy elderly individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695712/ https://www.ncbi.nlm.nih.gov/pubmed/33247134 http://dx.doi.org/10.1038/s41467-020-19543-w |
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