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Tau and atrophy: domain-specific relationships with cognition
BACKGROUND: Late-onset Alzheimer’s disease (AD) is characterized by primary memory impairment, which then progresses towards severe deficits across cognitive domains. Here, we report how performance in cognitive domains relates to patterns of tau deposition and cortical thickness. METHODS: We analyz...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661099/ https://www.ncbi.nlm.nih.gov/pubmed/31351484 http://dx.doi.org/10.1186/s13195-019-0518-8 |
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author | Digma, Leonardino A. Madsen, John R. Reas, Emilie T. Dale, Anders M. Brewer, James B. Banks, Sarah J. |
author_facet | Digma, Leonardino A. Madsen, John R. Reas, Emilie T. Dale, Anders M. Brewer, James B. Banks, Sarah J. |
author_sort | Digma, Leonardino A. |
collection | PubMed |
description | BACKGROUND: Late-onset Alzheimer’s disease (AD) is characterized by primary memory impairment, which then progresses towards severe deficits across cognitive domains. Here, we report how performance in cognitive domains relates to patterns of tau deposition and cortical thickness. METHODS: We analyzed data from 131 amyloid-β positive participants (55 cognitively normal, 46 mild cognitive impairment, 30 AD) of the Alzheimer’s Disease Neuroimaging Initiative who underwent magnetic resonance imaging (MRI), flortaucipir (FTP) positron emission tomography, and neuropsychological testing. Surface-based vertex-wise and region-of-interest analyses were conducted between FTP and cognitive test scores, and between cortical thickness and cognitive test scores. RESULTS: FTP and thickness were differentially related to cognitive performance in several domains. FTP-cognition associations were more widespread than thickness-cognition associations. Further, FTP-cognition patterns reflected cortical systems that underlie different aspects of cognition. CONCLUSIONS: Our findings indicate that AD-related decline in domain-specific cognitive performance reflects underlying progression of tau and atrophy into associated brain circuits. They also suggest that tau-PET may have better sensitivity to this decline than MRI-derived measures of cortical thickness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13195-019-0518-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6661099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66610992019-08-01 Tau and atrophy: domain-specific relationships with cognition Digma, Leonardino A. Madsen, John R. Reas, Emilie T. Dale, Anders M. Brewer, James B. Banks, Sarah J. Alzheimers Res Ther Research BACKGROUND: Late-onset Alzheimer’s disease (AD) is characterized by primary memory impairment, which then progresses towards severe deficits across cognitive domains. Here, we report how performance in cognitive domains relates to patterns of tau deposition and cortical thickness. METHODS: We analyzed data from 131 amyloid-β positive participants (55 cognitively normal, 46 mild cognitive impairment, 30 AD) of the Alzheimer’s Disease Neuroimaging Initiative who underwent magnetic resonance imaging (MRI), flortaucipir (FTP) positron emission tomography, and neuropsychological testing. Surface-based vertex-wise and region-of-interest analyses were conducted between FTP and cognitive test scores, and between cortical thickness and cognitive test scores. RESULTS: FTP and thickness were differentially related to cognitive performance in several domains. FTP-cognition associations were more widespread than thickness-cognition associations. Further, FTP-cognition patterns reflected cortical systems that underlie different aspects of cognition. CONCLUSIONS: Our findings indicate that AD-related decline in domain-specific cognitive performance reflects underlying progression of tau and atrophy into associated brain circuits. They also suggest that tau-PET may have better sensitivity to this decline than MRI-derived measures of cortical thickness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13195-019-0518-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-27 /pmc/articles/PMC6661099/ /pubmed/31351484 http://dx.doi.org/10.1186/s13195-019-0518-8 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 Digma, Leonardino A. Madsen, John R. Reas, Emilie T. Dale, Anders M. Brewer, James B. Banks, Sarah J. Tau and atrophy: domain-specific relationships with cognition |
title | Tau and atrophy: domain-specific relationships with cognition |
title_full | Tau and atrophy: domain-specific relationships with cognition |
title_fullStr | Tau and atrophy: domain-specific relationships with cognition |
title_full_unstemmed | Tau and atrophy: domain-specific relationships with cognition |
title_short | Tau and atrophy: domain-specific relationships with cognition |
title_sort | tau and atrophy: domain-specific relationships with cognition |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661099/ https://www.ncbi.nlm.nih.gov/pubmed/31351484 http://dx.doi.org/10.1186/s13195-019-0518-8 |
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