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Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology

INTRODUCTION: Structural magnetic resonance imaging is a marker of gray matter health and decline that is sensitive to impaired cognition and Alzheimer's disease pathology. Prior work has shown that both amyloid β (Aβ) and tau biomarkers are related to cortical thinning, but it is unclear what...

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Autores principales: Gordon, Brian A., McCullough, Austin, Mishra, Shruti, Blazey, Tyler M., Su, Yi, Christensen, John, Dincer, Aylin, Jackson, Kelley, Hornbeck, Russ C., Morris, John C., Ances, Beau M., Benzinger, Tammie L.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956934/
https://www.ncbi.nlm.nih.gov/pubmed/29780869
http://dx.doi.org/10.1016/j.dadm.2018.02.003
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author Gordon, Brian A.
McCullough, Austin
Mishra, Shruti
Blazey, Tyler M.
Su, Yi
Christensen, John
Dincer, Aylin
Jackson, Kelley
Hornbeck, Russ C.
Morris, John C.
Ances, Beau M.
Benzinger, Tammie L.S.
author_facet Gordon, Brian A.
McCullough, Austin
Mishra, Shruti
Blazey, Tyler M.
Su, Yi
Christensen, John
Dincer, Aylin
Jackson, Kelley
Hornbeck, Russ C.
Morris, John C.
Ances, Beau M.
Benzinger, Tammie L.S.
author_sort Gordon, Brian A.
collection PubMed
description INTRODUCTION: Structural magnetic resonance imaging is a marker of gray matter health and decline that is sensitive to impaired cognition and Alzheimer's disease pathology. Prior work has shown that both amyloid β (Aβ) and tau biomarkers are related to cortical thinning, but it is unclear what unique influences they have on the brain. METHODS: Aβ pathology was measured with [(18)F] AV-45 (florbetapir) positron emission tomography (PET) and tau was assessed with [(18)F] AV-1451 (flortaucipir) PET in a population of 178 older adults, of which 123 had longitudinal magnetic resonance imaging assessments (average of 5.7 years) that preceded the PET acquisitions. RESULTS: In cross-sectional analyses, greater tau PET pathology was associated with thinner cortices. When examined independently in longitudinal models, both Aβ and tau were associated with greater antecedent loss of gray matter. However, when examined in a combined model, levels of tau, but not Aβ, were still highly related to change in cortical thickness. DISCUSSION: Measures of tau PET are strongly related to gray matter atrophy and likely mediate relationships between Aβ and gray matter.
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spelling pubmed-59569342018-05-18 Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology Gordon, Brian A. McCullough, Austin Mishra, Shruti Blazey, Tyler M. Su, Yi Christensen, John Dincer, Aylin Jackson, Kelley Hornbeck, Russ C. Morris, John C. Ances, Beau M. Benzinger, Tammie L.S. Alzheimers Dement (Amst) Special Section: State of the Field: Advances in Neuroimaging from the 2017 Alzheimer’s Imaging Consortium. (Guest Editors: Drs. David Wolk, Victor Villemagne & Bradford Dickerson) INTRODUCTION: Structural magnetic resonance imaging is a marker of gray matter health and decline that is sensitive to impaired cognition and Alzheimer's disease pathology. Prior work has shown that both amyloid β (Aβ) and tau biomarkers are related to cortical thinning, but it is unclear what unique influences they have on the brain. METHODS: Aβ pathology was measured with [(18)F] AV-45 (florbetapir) positron emission tomography (PET) and tau was assessed with [(18)F] AV-1451 (flortaucipir) PET in a population of 178 older adults, of which 123 had longitudinal magnetic resonance imaging assessments (average of 5.7 years) that preceded the PET acquisitions. RESULTS: In cross-sectional analyses, greater tau PET pathology was associated with thinner cortices. When examined independently in longitudinal models, both Aβ and tau were associated with greater antecedent loss of gray matter. However, when examined in a combined model, levels of tau, but not Aβ, were still highly related to change in cortical thickness. DISCUSSION: Measures of tau PET are strongly related to gray matter atrophy and likely mediate relationships between Aβ and gray matter. Elsevier 2018-03-06 /pmc/articles/PMC5956934/ /pubmed/29780869 http://dx.doi.org/10.1016/j.dadm.2018.02.003 Text en © 2018 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 Special Section: State of the Field: Advances in Neuroimaging from the 2017 Alzheimer’s Imaging Consortium. (Guest Editors: Drs. David Wolk, Victor Villemagne & Bradford Dickerson)
Gordon, Brian A.
McCullough, Austin
Mishra, Shruti
Blazey, Tyler M.
Su, Yi
Christensen, John
Dincer, Aylin
Jackson, Kelley
Hornbeck, Russ C.
Morris, John C.
Ances, Beau M.
Benzinger, Tammie L.S.
Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
title Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
title_full Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
title_fullStr Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
title_full_unstemmed Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
title_short Cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
title_sort cross-sectional and longitudinal atrophy is preferentially associated with tau rather than amyloid β positron emission tomography pathology
topic Special Section: State of the Field: Advances in Neuroimaging from the 2017 Alzheimer’s Imaging Consortium. (Guest Editors: Drs. David Wolk, Victor Villemagne & Bradford Dickerson)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956934/
https://www.ncbi.nlm.nih.gov/pubmed/29780869
http://dx.doi.org/10.1016/j.dadm.2018.02.003
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