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Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease
BACKGROUND: We aimed to investigate the clinical correlates of principal components (PCs) of tau positron emission tomography (PET) and their predictability for longitudinal changes in tau accumulation in Alzheimer’s disease (AD). METHODS: We enrolled 272 participants who underwent two PET scans [(1...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513482/ https://www.ncbi.nlm.nih.gov/pubmed/32967721 http://dx.doi.org/10.1186/s13195-020-00685-4 |
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author | Cho, Hanna Baek, Min Seok Lee, Hye Sun Lee, Jae Hoon Ryu, Young Hoon Lyoo, Chul Hyoung |
author_facet | Cho, Hanna Baek, Min Seok Lee, Hye Sun Lee, Jae Hoon Ryu, Young Hoon Lyoo, Chul Hyoung |
author_sort | Cho, Hanna |
collection | PubMed |
description | BACKGROUND: We aimed to investigate the clinical correlates of principal components (PCs) of tau positron emission tomography (PET) and their predictability for longitudinal changes in tau accumulation in Alzheimer’s disease (AD). METHODS: We enrolled 272 participants who underwent two PET scans [(18)F-flortaucipir for tau and (18)F-florbetaben for amyloid-β (Aβ)], brain magnetic resonance imaging, and neuropsychological tests as baseline assessments. Among them, 187 participants underwent the same follow-up assessments after an average of 2 years. Using Aβ-positive AD dementia-specific PCs obtained from the baseline scans of 56 Aβ-positive patients with AD dementia, we determined the expression of the first two PCs (PC1 and PC2) in all participants. We assessed the correlation of PC expression with baseline clinical characteristics and tau accumulation rates. Moreover, we investigated the predictability of PCs for the longitudinal tau accumulation in training and test sets. RESULTS: PC1 corresponded to the tau distribution pattern in AD, while the two PC2 extremes reflected the parietal or temporal predominance of tau distribution. PC1 expression increased with tau burden and decreased with cognitive impairment, while PC2 expression decreased with advanced age and visuospatial and attention function deterioration. The tau accumulation rate was positively correlated with PC1 expression (greater tau burden) and negatively correlated with PC2 expression (temporal predominance). A regression model using both PCs could predict longitudinal changes in the tau burden (intraclass correlation coefficient = 0.775, R(2) = 0.456 in test set). CONCLUSIONS: PC analysis of tau PET could be useful for evaluating disease progression, characterizing the tau distribution pattern, and predicting longitudinal tau accumulation. |
format | Online Article Text |
id | pubmed-7513482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75134822020-09-25 Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease Cho, Hanna Baek, Min Seok Lee, Hye Sun Lee, Jae Hoon Ryu, Young Hoon Lyoo, Chul Hyoung Alzheimers Res Ther Research BACKGROUND: We aimed to investigate the clinical correlates of principal components (PCs) of tau positron emission tomography (PET) and their predictability for longitudinal changes in tau accumulation in Alzheimer’s disease (AD). METHODS: We enrolled 272 participants who underwent two PET scans [(18)F-flortaucipir for tau and (18)F-florbetaben for amyloid-β (Aβ)], brain magnetic resonance imaging, and neuropsychological tests as baseline assessments. Among them, 187 participants underwent the same follow-up assessments after an average of 2 years. Using Aβ-positive AD dementia-specific PCs obtained from the baseline scans of 56 Aβ-positive patients with AD dementia, we determined the expression of the first two PCs (PC1 and PC2) in all participants. We assessed the correlation of PC expression with baseline clinical characteristics and tau accumulation rates. Moreover, we investigated the predictability of PCs for the longitudinal tau accumulation in training and test sets. RESULTS: PC1 corresponded to the tau distribution pattern in AD, while the two PC2 extremes reflected the parietal or temporal predominance of tau distribution. PC1 expression increased with tau burden and decreased with cognitive impairment, while PC2 expression decreased with advanced age and visuospatial and attention function deterioration. The tau accumulation rate was positively correlated with PC1 expression (greater tau burden) and negatively correlated with PC2 expression (temporal predominance). A regression model using both PCs could predict longitudinal changes in the tau burden (intraclass correlation coefficient = 0.775, R(2) = 0.456 in test set). CONCLUSIONS: PC analysis of tau PET could be useful for evaluating disease progression, characterizing the tau distribution pattern, and predicting longitudinal tau accumulation. BioMed Central 2020-09-23 /pmc/articles/PMC7513482/ /pubmed/32967721 http://dx.doi.org/10.1186/s13195-020-00685-4 Text en © The Author(s) 2020 Open AccessThis 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/. 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 in a credit line to the data. |
spellingShingle | Research Cho, Hanna Baek, Min Seok Lee, Hye Sun Lee, Jae Hoon Ryu, Young Hoon Lyoo, Chul Hyoung Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease |
title | Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease |
title_full | Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease |
title_fullStr | Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease |
title_full_unstemmed | Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease |
title_short | Principal components of tau positron emission tomography and longitudinal tau accumulation in Alzheimer’s disease |
title_sort | principal components of tau positron emission tomography and longitudinal tau accumulation in alzheimer’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513482/ https://www.ncbi.nlm.nih.gov/pubmed/32967721 http://dx.doi.org/10.1186/s13195-020-00685-4 |
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