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Tau pathology in cognitively normal older adults

INTRODUCTION: Tau pathology, a hallmark of Alzheimer's disease, is observed in the brains of virtually all individuals over 70 years. METHODS: Using (18)F-AV-1451 ((18)F-flortaucipir) positron emission tomography, we evaluated tau pathology in 54 cognitively normal participants (mean age: 77.5...

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Autores principales: Ziontz, Jacob, Bilgel, Murat, Shafer, Andrea T., Moghekar, Abhay, Elkins, Wendy, Helphrey, Jessica, Gomez, Gabriela, June, Danielle, McDonald, Michael A., Dannals, Robert F., Azad, Babak Behnam, Ferrucci, Luigi, Wong, Dean F., Resnick, Susan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732758/
https://www.ncbi.nlm.nih.gov/pubmed/31517026
http://dx.doi.org/10.1016/j.dadm.2019.07.007
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author Ziontz, Jacob
Bilgel, Murat
Shafer, Andrea T.
Moghekar, Abhay
Elkins, Wendy
Helphrey, Jessica
Gomez, Gabriela
June, Danielle
McDonald, Michael A.
Dannals, Robert F.
Azad, Babak Behnam
Ferrucci, Luigi
Wong, Dean F.
Resnick, Susan M.
author_facet Ziontz, Jacob
Bilgel, Murat
Shafer, Andrea T.
Moghekar, Abhay
Elkins, Wendy
Helphrey, Jessica
Gomez, Gabriela
June, Danielle
McDonald, Michael A.
Dannals, Robert F.
Azad, Babak Behnam
Ferrucci, Luigi
Wong, Dean F.
Resnick, Susan M.
author_sort Ziontz, Jacob
collection PubMed
description INTRODUCTION: Tau pathology, a hallmark of Alzheimer's disease, is observed in the brains of virtually all individuals over 70 years. METHODS: Using (18)F-AV-1451 ((18)F-flortaucipir) positron emission tomography, we evaluated tau pathology in 54 cognitively normal participants (mean age: 77.5 years, SD: 8.9) from the Baltimore Longitudinal Study of Aging. We assessed associations between positron emission tomography signal and age, sex, race, and amyloid positivity. We investigated relationships between regional signal and retrospective rates of change in regional volumes and cognitive function adjusting for age, sex, and amyloid status. RESULTS: Greater age, male sex, black race, and amyloid positivity were associated with higher (18)F-AV-1451 retention in distinct brain regions. Retention in the entorhinal cortex was associated with lower entorhinal volume (β = −1.124, SE = 0.485, P = .025) and a steeper decline in memory performance (β = −0.086, SE = 0.039, P = .029). DISCUSSION: Assessment of medial temporal tau pathology will provide insights into early structural brain changes associated with later cognitive impairment and Alzheimer's disease.
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spelling pubmed-67327582019-09-12 Tau pathology in cognitively normal older adults Ziontz, Jacob Bilgel, Murat Shafer, Andrea T. Moghekar, Abhay Elkins, Wendy Helphrey, Jessica Gomez, Gabriela June, Danielle McDonald, Michael A. Dannals, Robert F. Azad, Babak Behnam Ferrucci, Luigi Wong, Dean F. Resnick, Susan M. Alzheimers Dement (Amst) Neuroimaging INTRODUCTION: Tau pathology, a hallmark of Alzheimer's disease, is observed in the brains of virtually all individuals over 70 years. METHODS: Using (18)F-AV-1451 ((18)F-flortaucipir) positron emission tomography, we evaluated tau pathology in 54 cognitively normal participants (mean age: 77.5 years, SD: 8.9) from the Baltimore Longitudinal Study of Aging. We assessed associations between positron emission tomography signal and age, sex, race, and amyloid positivity. We investigated relationships between regional signal and retrospective rates of change in regional volumes and cognitive function adjusting for age, sex, and amyloid status. RESULTS: Greater age, male sex, black race, and amyloid positivity were associated with higher (18)F-AV-1451 retention in distinct brain regions. Retention in the entorhinal cortex was associated with lower entorhinal volume (β = −1.124, SE = 0.485, P = .025) and a steeper decline in memory performance (β = −0.086, SE = 0.039, P = .029). DISCUSSION: Assessment of medial temporal tau pathology will provide insights into early structural brain changes associated with later cognitive impairment and Alzheimer's disease. Elsevier 2019-09-06 /pmc/articles/PMC6732758/ /pubmed/31517026 http://dx.doi.org/10.1016/j.dadm.2019.07.007 Text en 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 Neuroimaging
Ziontz, Jacob
Bilgel, Murat
Shafer, Andrea T.
Moghekar, Abhay
Elkins, Wendy
Helphrey, Jessica
Gomez, Gabriela
June, Danielle
McDonald, Michael A.
Dannals, Robert F.
Azad, Babak Behnam
Ferrucci, Luigi
Wong, Dean F.
Resnick, Susan M.
Tau pathology in cognitively normal older adults
title Tau pathology in cognitively normal older adults
title_full Tau pathology in cognitively normal older adults
title_fullStr Tau pathology in cognitively normal older adults
title_full_unstemmed Tau pathology in cognitively normal older adults
title_short Tau pathology in cognitively normal older adults
title_sort tau pathology in cognitively normal older adults
topic Neuroimaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732758/
https://www.ncbi.nlm.nih.gov/pubmed/31517026
http://dx.doi.org/10.1016/j.dadm.2019.07.007
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