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Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume

OBJECTIVE: To test the hypothesis that the combination of elevated global β-AMYLOID (Aβ) burden and greater striatal iron content would be associated with smaller entorhinal cortex (ERC) volume, but not hippocampal subfield volumes, we measured volume and iron content using high-resolution MRI and A...

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Autores principales: Foster, Chris M., Kennedy, Kristen M., Daugherty, Ana M., Rodrigue, Karen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682827/
https://www.ncbi.nlm.nih.gov/pubmed/32938781
http://dx.doi.org/10.1212/WNL.0000000000010868
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author Foster, Chris M.
Kennedy, Kristen M.
Daugherty, Ana M.
Rodrigue, Karen M.
author_facet Foster, Chris M.
Kennedy, Kristen M.
Daugherty, Ana M.
Rodrigue, Karen M.
author_sort Foster, Chris M.
collection PubMed
description OBJECTIVE: To test the hypothesis that the combination of elevated global β-AMYLOID (Aβ) burden and greater striatal iron content would be associated with smaller entorhinal cortex (ERC) volume, but not hippocampal subfield volumes, we measured volume and iron content using high-resolution MRI and Aβ using PET imaging in a cross-sectional sample of 70 cognitively normal older adults. METHODS: Participants were scanned with florbetapir (18)F PET to obtain Aβ standardized uptake value ratios. Susceptibility-weighted MRI was collected and processed to yield R2* images, and striatal regions of interest (ROIs) were manually placed to obtain a measure of striatal iron burden. Ultra-high resolution T2/PD-weighted MRIs were segmented to measure medial temporal lobe (MTL) volumes. Analyses were conducted using mixed-effects models with MTL ROI as a within-participant factor; age, iron content, and Aβ as between-participant factors; and MTL volumes (ERC and 3 hippocampal subfield regions) as the dependent variable. RESULTS: The model indicated a significant 4-way interaction among age, iron, Aβ, and MTL region. Post hoc analyses indicated that the 3-way interaction among age, Aβ, and iron content was selective to the ERC (β = −3.34, standard error = 1.33, 95% confidence interval −5.95 to −0.72), whereas a significant negative association between age and ERC volume was present only in individuals with both elevated iron content and Aβ. CONCLUSIONS: These findings highlight the importance of studying Aβ in the context of other, potentially synergistic age-related brain factors such as iron accumulation and the potential role for iron as an important contributor to the earliest, preclinical stages of pathologic aging.
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spelling pubmed-76828272020-11-24 Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume Foster, Chris M. Kennedy, Kristen M. Daugherty, Ana M. Rodrigue, Karen M. Neurology Article OBJECTIVE: To test the hypothesis that the combination of elevated global β-AMYLOID (Aβ) burden and greater striatal iron content would be associated with smaller entorhinal cortex (ERC) volume, but not hippocampal subfield volumes, we measured volume and iron content using high-resolution MRI and Aβ using PET imaging in a cross-sectional sample of 70 cognitively normal older adults. METHODS: Participants were scanned with florbetapir (18)F PET to obtain Aβ standardized uptake value ratios. Susceptibility-weighted MRI was collected and processed to yield R2* images, and striatal regions of interest (ROIs) were manually placed to obtain a measure of striatal iron burden. Ultra-high resolution T2/PD-weighted MRIs were segmented to measure medial temporal lobe (MTL) volumes. Analyses were conducted using mixed-effects models with MTL ROI as a within-participant factor; age, iron content, and Aβ as between-participant factors; and MTL volumes (ERC and 3 hippocampal subfield regions) as the dependent variable. RESULTS: The model indicated a significant 4-way interaction among age, iron, Aβ, and MTL region. Post hoc analyses indicated that the 3-way interaction among age, Aβ, and iron content was selective to the ERC (β = −3.34, standard error = 1.33, 95% confidence interval −5.95 to −0.72), whereas a significant negative association between age and ERC volume was present only in individuals with both elevated iron content and Aβ. CONCLUSIONS: These findings highlight the importance of studying Aβ in the context of other, potentially synergistic age-related brain factors such as iron accumulation and the potential role for iron as an important contributor to the earliest, preclinical stages of pathologic aging. Lippincott Williams & Wilkins 2020-11-03 /pmc/articles/PMC7682827/ /pubmed/32938781 http://dx.doi.org/10.1212/WNL.0000000000010868 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Foster, Chris M.
Kennedy, Kristen M.
Daugherty, Ana M.
Rodrigue, Karen M.
Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume
title Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume
title_full Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume
title_fullStr Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume
title_full_unstemmed Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume
title_short Contribution of iron and Aβ to age differences in entorhinal and hippocampal subfield volume
title_sort contribution of iron and aβ to age differences in entorhinal and hippocampal subfield volume
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682827/
https://www.ncbi.nlm.nih.gov/pubmed/32938781
http://dx.doi.org/10.1212/WNL.0000000000010868
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