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Tau oligomers in cerebrospinal fluid in Alzheimer's disease
OBJECTIVE: With an increasing incidence of Alzheimer's disease (AD) and neurodegenerative tauopathies, there is an urgent need to develop reliable biomarkers for the diagnosis and monitoring of the disease, such as the recently discovered toxic tau oligomers. Here, we aimed to demonstrate the p...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376754/ https://www.ncbi.nlm.nih.gov/pubmed/28382304 http://dx.doi.org/10.1002/acn3.382 |
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author | Sengupta, Urmi Portelius, Erik Hansson, Oskar Farmer, Kathleen Castillo‐Carranza, Diana Woltjer, Randall Zetterberg, Henrik Galasko, Douglas Blennow, Kaj Kayed, Rakez |
author_facet | Sengupta, Urmi Portelius, Erik Hansson, Oskar Farmer, Kathleen Castillo‐Carranza, Diana Woltjer, Randall Zetterberg, Henrik Galasko, Douglas Blennow, Kaj Kayed, Rakez |
author_sort | Sengupta, Urmi |
collection | PubMed |
description | OBJECTIVE: With an increasing incidence of Alzheimer's disease (AD) and neurodegenerative tauopathies, there is an urgent need to develop reliable biomarkers for the diagnosis and monitoring of the disease, such as the recently discovered toxic tau oligomers. Here, we aimed to demonstrate the presence of tau oligomers in the cerebrospinal fluid (CSF) of patients with cognitive deficits, and to determine whether tau oligomers could serve as a potential biomarker for AD. METHODS: A multicentric collaborative study involving a double‐blinded analysis with a total of 98 subjects with moderate to severe AD (N = 41), mild AD (N = 31), and nondemented control subjects (N = 26), and two pilot studies of 33 total patients with AD (N = 19) and control (N = 14) subjects were performed. We carried out biochemical assays to measure oligomeric tau from CSF of these patients with various degrees of cognitive impairment as well as cognitively normal controls. RESULTS: Using a highly reproducible indirect ELISA method, we found elevated levels of tau oligomers in AD patients compared to age‐matched controls. Western blot analysis confirmed the presence of oligomeric forms of tau in CSF. In addition, the ratio of oligomeric to total tau increased in the order: moderate to severe AD, mild AD, and controls. CONCLUSION: These assays are suitable for the analysis of human CSF samples. These results here suggest that CSF tau oligomer measurements could be optimized and added to the panel of CSF biomarkers for the accurate and early detection of AD. |
format | Online Article Text |
id | pubmed-5376754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53767542017-04-05 Tau oligomers in cerebrospinal fluid in Alzheimer's disease Sengupta, Urmi Portelius, Erik Hansson, Oskar Farmer, Kathleen Castillo‐Carranza, Diana Woltjer, Randall Zetterberg, Henrik Galasko, Douglas Blennow, Kaj Kayed, Rakez Ann Clin Transl Neurol Research Articles OBJECTIVE: With an increasing incidence of Alzheimer's disease (AD) and neurodegenerative tauopathies, there is an urgent need to develop reliable biomarkers for the diagnosis and monitoring of the disease, such as the recently discovered toxic tau oligomers. Here, we aimed to demonstrate the presence of tau oligomers in the cerebrospinal fluid (CSF) of patients with cognitive deficits, and to determine whether tau oligomers could serve as a potential biomarker for AD. METHODS: A multicentric collaborative study involving a double‐blinded analysis with a total of 98 subjects with moderate to severe AD (N = 41), mild AD (N = 31), and nondemented control subjects (N = 26), and two pilot studies of 33 total patients with AD (N = 19) and control (N = 14) subjects were performed. We carried out biochemical assays to measure oligomeric tau from CSF of these patients with various degrees of cognitive impairment as well as cognitively normal controls. RESULTS: Using a highly reproducible indirect ELISA method, we found elevated levels of tau oligomers in AD patients compared to age‐matched controls. Western blot analysis confirmed the presence of oligomeric forms of tau in CSF. In addition, the ratio of oligomeric to total tau increased in the order: moderate to severe AD, mild AD, and controls. CONCLUSION: These assays are suitable for the analysis of human CSF samples. These results here suggest that CSF tau oligomer measurements could be optimized and added to the panel of CSF biomarkers for the accurate and early detection of AD. John Wiley and Sons Inc. 2017-03-01 /pmc/articles/PMC5376754/ /pubmed/28382304 http://dx.doi.org/10.1002/acn3.382 Text en © 2017 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Sengupta, Urmi Portelius, Erik Hansson, Oskar Farmer, Kathleen Castillo‐Carranza, Diana Woltjer, Randall Zetterberg, Henrik Galasko, Douglas Blennow, Kaj Kayed, Rakez Tau oligomers in cerebrospinal fluid in Alzheimer's disease |
title | Tau oligomers in cerebrospinal fluid in Alzheimer's disease |
title_full | Tau oligomers in cerebrospinal fluid in Alzheimer's disease |
title_fullStr | Tau oligomers in cerebrospinal fluid in Alzheimer's disease |
title_full_unstemmed | Tau oligomers in cerebrospinal fluid in Alzheimer's disease |
title_short | Tau oligomers in cerebrospinal fluid in Alzheimer's disease |
title_sort | tau oligomers in cerebrospinal fluid in alzheimer's disease |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376754/ https://www.ncbi.nlm.nih.gov/pubmed/28382304 http://dx.doi.org/10.1002/acn3.382 |
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