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Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study

INTRODUCTION: Amyloid-β (Aβ) and tau accumulations may occur independently and concurrently as exemplified by primary age-related tauopathy and Alzheimer's disease (AD), respectively. Interactions between Aβ and tau accumulations and their influence on clinical features, however, are still uncl...

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Autores principales: Shimada, Hitoshi, Kitamura, Soichiro, Shinotoh, Hitoshi, Endo, Hironobu, Niwa, Fumitoshi, Hirano, Shigeki, Kimura, Yasuyuki, Zhang, Ming-Rong, Kuwabara, Satoshi, Suhara, Tetsuya, Higuchi, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5257028/
https://www.ncbi.nlm.nih.gov/pubmed/28138509
http://dx.doi.org/10.1016/j.dadm.2016.12.009
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author Shimada, Hitoshi
Kitamura, Soichiro
Shinotoh, Hitoshi
Endo, Hironobu
Niwa, Fumitoshi
Hirano, Shigeki
Kimura, Yasuyuki
Zhang, Ming-Rong
Kuwabara, Satoshi
Suhara, Tetsuya
Higuchi, Makoto
author_facet Shimada, Hitoshi
Kitamura, Soichiro
Shinotoh, Hitoshi
Endo, Hironobu
Niwa, Fumitoshi
Hirano, Shigeki
Kimura, Yasuyuki
Zhang, Ming-Rong
Kuwabara, Satoshi
Suhara, Tetsuya
Higuchi, Makoto
author_sort Shimada, Hitoshi
collection PubMed
description INTRODUCTION: Amyloid-β (Aβ) and tau accumulations may occur independently and concurrently as exemplified by primary age-related tauopathy and Alzheimer's disease (AD), respectively. Interactions between Aβ and tau accumulations and their influence on clinical features, however, are still unclear. METHODS: Associations among clinical symptoms, gray-matter volume, regional tau, and Aβ deposition assessed by positron emission tomography with [(11)C]pyridinyl-butadienyl-benzothiazole 3 (PBB3) and [(11)C]Pittsburgh compound-B (PiB), were evaluated in 17 AD, 9 mild cognitive impairment due to AD, and 28 PiB(−)-cognitive healthy controls (HCs). RESULTS: High tau burden was associated with aging and low-level education in PiB(−)-HC and AD-spectrum groups, and with high Aβ burden and low-level education in all subjects. It was not Aβ but tau accumulation that showed significant associations with cognitive performance even in PiB(−)-HC. DISCUSSION: The present study indicated aging and low-level education after Aβ would be enhancers for tau pathology, associated with neurodegeneration and cognitive impairment in healthy and diseased elderly individuals.
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spelling pubmed-52570282017-01-30 Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study Shimada, Hitoshi Kitamura, Soichiro Shinotoh, Hitoshi Endo, Hironobu Niwa, Fumitoshi Hirano, Shigeki Kimura, Yasuyuki Zhang, Ming-Rong Kuwabara, Satoshi Suhara, Tetsuya Higuchi, Makoto Alzheimers Dement (Amst) PART II. State of the Field: Advances in Neuroimaging from the 2016 Alzheimer's Imaging Consortium INTRODUCTION: Amyloid-β (Aβ) and tau accumulations may occur independently and concurrently as exemplified by primary age-related tauopathy and Alzheimer's disease (AD), respectively. Interactions between Aβ and tau accumulations and their influence on clinical features, however, are still unclear. METHODS: Associations among clinical symptoms, gray-matter volume, regional tau, and Aβ deposition assessed by positron emission tomography with [(11)C]pyridinyl-butadienyl-benzothiazole 3 (PBB3) and [(11)C]Pittsburgh compound-B (PiB), were evaluated in 17 AD, 9 mild cognitive impairment due to AD, and 28 PiB(−)-cognitive healthy controls (HCs). RESULTS: High tau burden was associated with aging and low-level education in PiB(−)-HC and AD-spectrum groups, and with high Aβ burden and low-level education in all subjects. It was not Aβ but tau accumulation that showed significant associations with cognitive performance even in PiB(−)-HC. DISCUSSION: The present study indicated aging and low-level education after Aβ would be enhancers for tau pathology, associated with neurodegeneration and cognitive impairment in healthy and diseased elderly individuals. Elsevier 2016-12-22 /pmc/articles/PMC5257028/ /pubmed/28138509 http://dx.doi.org/10.1016/j.dadm.2016.12.009 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle PART II. State of the Field: Advances in Neuroimaging from the 2016 Alzheimer's Imaging Consortium
Shimada, Hitoshi
Kitamura, Soichiro
Shinotoh, Hitoshi
Endo, Hironobu
Niwa, Fumitoshi
Hirano, Shigeki
Kimura, Yasuyuki
Zhang, Ming-Rong
Kuwabara, Satoshi
Suhara, Tetsuya
Higuchi, Makoto
Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study
title Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study
title_full Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study
title_fullStr Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study
title_full_unstemmed Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study
title_short Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [(11)C]PBB3-PET study
title_sort association between aβ and tau accumulations and their influence on clinical features in aging and alzheimer's disease spectrum brains: a [(11)c]pbb3-pet study
topic PART II. State of the Field: Advances in Neuroimaging from the 2016 Alzheimer's Imaging Consortium
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5257028/
https://www.ncbi.nlm.nih.gov/pubmed/28138509
http://dx.doi.org/10.1016/j.dadm.2016.12.009
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