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Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease
INTRODUCTION: Longitudinal positron emission tomography (PET) studies of tau accumulation in Alzheimer's disease (AD) have noted reduced increases or frank decreases in tau signal. We investigated how such reductions related to analytical confounds and disease progression markers in atypical AD...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292954/ https://www.ncbi.nlm.nih.gov/pubmed/34515411 http://dx.doi.org/10.1002/alz.12456 |
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author | Phillips, Jeffrey S. Nitchie, Frederick J. Da Re, Fulvio Olm, Christopher A. Cook, Philip A. McMillan, Corey T. Irwin, David J. Gee, James C. Dubroff, Jacob G. Grossman, Murray Nasrallah, Ilya M. |
author_facet | Phillips, Jeffrey S. Nitchie, Frederick J. Da Re, Fulvio Olm, Christopher A. Cook, Philip A. McMillan, Corey T. Irwin, David J. Gee, James C. Dubroff, Jacob G. Grossman, Murray Nasrallah, Ilya M. |
author_sort | Phillips, Jeffrey S. |
collection | PubMed |
description | INTRODUCTION: Longitudinal positron emission tomography (PET) studies of tau accumulation in Alzheimer's disease (AD) have noted reduced increases or frank decreases in tau signal. We investigated how such reductions related to analytical confounds and disease progression markers in atypical AD. METHODS: We assessed regional and interindividual variation in longitudinal change on (18)F‐flortaucipir PET imaging in 24 amyloid beta (Aβ)+ patients with atypical, early‐onset amnestic or non‐amnestic AD plus 62 Aβ– and 132 Aβ+ Alzheimer's Disease Neuroimaging Initiative (ADNI) participants. RESULTS: In atypical AD, (18)F‐flortaucipir uptake slowed or declined over time in areas with high baseline signal and older, more impaired individuals. ADNI participants had reduced longitudinal change in early Braak stage regions relative to late‐stage areas. DISCUSSION: Results suggested radioligand uptake plateaus or declines in advanced neurodegeneration. Further research should investigate whether results generalize to other radioligands and whether they relate to changes of the radioligand binding site structure or accessibility. |
format | Online Article Text |
id | pubmed-9292954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92929542022-07-20 Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease Phillips, Jeffrey S. Nitchie, Frederick J. Da Re, Fulvio Olm, Christopher A. Cook, Philip A. McMillan, Corey T. Irwin, David J. Gee, James C. Dubroff, Jacob G. Grossman, Murray Nasrallah, Ilya M. Alzheimers Dement Featured Articles INTRODUCTION: Longitudinal positron emission tomography (PET) studies of tau accumulation in Alzheimer's disease (AD) have noted reduced increases or frank decreases in tau signal. We investigated how such reductions related to analytical confounds and disease progression markers in atypical AD. METHODS: We assessed regional and interindividual variation in longitudinal change on (18)F‐flortaucipir PET imaging in 24 amyloid beta (Aβ)+ patients with atypical, early‐onset amnestic or non‐amnestic AD plus 62 Aβ– and 132 Aβ+ Alzheimer's Disease Neuroimaging Initiative (ADNI) participants. RESULTS: In atypical AD, (18)F‐flortaucipir uptake slowed or declined over time in areas with high baseline signal and older, more impaired individuals. ADNI participants had reduced longitudinal change in early Braak stage regions relative to late‐stage areas. DISCUSSION: Results suggested radioligand uptake plateaus or declines in advanced neurodegeneration. Further research should investigate whether results generalize to other radioligands and whether they relate to changes of the radioligand binding site structure or accessibility. John Wiley and Sons Inc. 2021-09-13 2022-06 /pmc/articles/PMC9292954/ /pubmed/34515411 http://dx.doi.org/10.1002/alz.12456 Text en © 2021 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 | Featured Articles Phillips, Jeffrey S. Nitchie, Frederick J. Da Re, Fulvio Olm, Christopher A. Cook, Philip A. McMillan, Corey T. Irwin, David J. Gee, James C. Dubroff, Jacob G. Grossman, Murray Nasrallah, Ilya M. Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease |
title | Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease |
title_full | Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease |
title_fullStr | Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease |
title_full_unstemmed | Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease |
title_short | Rates of longitudinal change in (18)F‐flortaucipir PET vary by brain region, cognitive impairment, and age in atypical Alzheimer's disease |
title_sort | rates of longitudinal change in (18)f‐flortaucipir pet vary by brain region, cognitive impairment, and age in atypical alzheimer's disease |
topic | Featured Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292954/ https://www.ncbi.nlm.nih.gov/pubmed/34515411 http://dx.doi.org/10.1002/alz.12456 |
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