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Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration

There has been increasing interest in finding non-invasive biomarkers for neurodegenerative diseases such as Alzheimer’s disease (AD). This observational study investigated AD-specific biomarkers in tear fluid. Tear fluid was collected from a total of 65 subjects, including 23 patients with subjecti...

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Autores principales: Gijs, Marlies, Ramakers, Inez H. G. B., Visser, Pieter Jelle, Verhey, Frans R. J., van de Waarenburg, Marjo P. H., Schalkwijk, Casper G., Nuijts, Rudy M. M. A., Webers, Carroll A. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8608861/
https://www.ncbi.nlm.nih.gov/pubmed/34811435
http://dx.doi.org/10.1038/s41598-021-01993-x
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author Gijs, Marlies
Ramakers, Inez H. G. B.
Visser, Pieter Jelle
Verhey, Frans R. J.
van de Waarenburg, Marjo P. H.
Schalkwijk, Casper G.
Nuijts, Rudy M. M. A.
Webers, Carroll A. B.
author_facet Gijs, Marlies
Ramakers, Inez H. G. B.
Visser, Pieter Jelle
Verhey, Frans R. J.
van de Waarenburg, Marjo P. H.
Schalkwijk, Casper G.
Nuijts, Rudy M. M. A.
Webers, Carroll A. B.
author_sort Gijs, Marlies
collection PubMed
description There has been increasing interest in finding non-invasive biomarkers for neurodegenerative diseases such as Alzheimer’s disease (AD). This observational study investigated AD-specific biomarkers in tear fluid. Tear fluid was collected from a total of 65 subjects, including 23 patients with subjective cognitive decline (SCD), 22 patients with mild cognitive impairment (MCI), 11 dementia patients and 9 healthy controls (HC). Levels of amyloid-beta peptides (AB38, AB40, AB42), total-tau (t-tau) and phosphorylated-tau (p-tau) were determined using multiplex immunoassays. Levels of AB40 and t-tau were detectable in the vast majority (> 94%) of tear fluid samples. Cerebrospinal fluid (CSF) was available from a subset of patients. In this group, tear t-tau levels were significantly higher in people with dementia compared to SCD patients. Tear t-tau levels were elevated in patients with neurodegeneration (classified according to the A/T/N system) compared to patients without neurodegeneration. Negative correlations were found between CSF AB42 and CSF t-tau, and between CSF AB42 and tear t-tau. In summary, this study shows the potential of tau proteins in tear fluid to be associated with disease severity and neurodegeneration.
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spelling pubmed-86088612021-11-24 Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration Gijs, Marlies Ramakers, Inez H. G. B. Visser, Pieter Jelle Verhey, Frans R. J. van de Waarenburg, Marjo P. H. Schalkwijk, Casper G. Nuijts, Rudy M. M. A. Webers, Carroll A. B. Sci Rep Article There has been increasing interest in finding non-invasive biomarkers for neurodegenerative diseases such as Alzheimer’s disease (AD). This observational study investigated AD-specific biomarkers in tear fluid. Tear fluid was collected from a total of 65 subjects, including 23 patients with subjective cognitive decline (SCD), 22 patients with mild cognitive impairment (MCI), 11 dementia patients and 9 healthy controls (HC). Levels of amyloid-beta peptides (AB38, AB40, AB42), total-tau (t-tau) and phosphorylated-tau (p-tau) were determined using multiplex immunoassays. Levels of AB40 and t-tau were detectable in the vast majority (> 94%) of tear fluid samples. Cerebrospinal fluid (CSF) was available from a subset of patients. In this group, tear t-tau levels were significantly higher in people with dementia compared to SCD patients. Tear t-tau levels were elevated in patients with neurodegeneration (classified according to the A/T/N system) compared to patients without neurodegeneration. Negative correlations were found between CSF AB42 and CSF t-tau, and between CSF AB42 and tear t-tau. In summary, this study shows the potential of tau proteins in tear fluid to be associated with disease severity and neurodegeneration. Nature Publishing Group UK 2021-11-22 /pmc/articles/PMC8608861/ /pubmed/34811435 http://dx.doi.org/10.1038/s41598-021-01993-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gijs, Marlies
Ramakers, Inez H. G. B.
Visser, Pieter Jelle
Verhey, Frans R. J.
van de Waarenburg, Marjo P. H.
Schalkwijk, Casper G.
Nuijts, Rudy M. M. A.
Webers, Carroll A. B.
Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
title Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
title_full Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
title_fullStr Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
title_full_unstemmed Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
title_short Association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
title_sort association of tear fluid amyloid and tau levels with disease severity and neurodegeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8608861/
https://www.ncbi.nlm.nih.gov/pubmed/34811435
http://dx.doi.org/10.1038/s41598-021-01993-x
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