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Cerebral Microstructure in Aging Using Advanced Quantitative MRI
White matter (WM) maintenance through oligodendrocyte metabolism is an energy-intensive process. Myelin homeostasis is sensitive to hypoxia, ischemia, or hypoperfusion. Besides substrate delivery, adequate cerebral blood flow (CBF) is crucial for removal of metabolic byproducts such as iron. While s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743490/ http://dx.doi.org/10.1093/geroni/igaa057.2771 |
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author | Bouhrara, Mustapha Khattar, Nikkita Kim, Richard Qian, Wenshu Alisch, Joseph Ferrucci, Luigi Resnick, Susan Spencer, Richard |
author_facet | Bouhrara, Mustapha Khattar, Nikkita Kim, Richard Qian, Wenshu Alisch, Joseph Ferrucci, Luigi Resnick, Susan Spencer, Richard |
author_sort | Bouhrara, Mustapha |
collection | PubMed |
description | White matter (WM) maintenance through oligodendrocyte metabolism is an energy-intensive process. Myelin homeostasis is sensitive to hypoxia, ischemia, or hypoperfusion. Besides substrate delivery, adequate cerebral blood flow (CBF) is crucial for removal of metabolic byproducts such as iron. While some data show decreased myelin content and CBF with aging, the association between CBF and myelination is unknown. Further, breakdown of oligodendrocyte and iron may potentiate myelin loss through oxidative mechanisms. Whether iron deposition is related to myelination is unclear. Using advanced MRI methodology, we investigated associations between CBF deficits, myelin loss, and iron deposition in cognitively normal individuals. We found significant association between i) CBF deficits and myelin loss (N=67,age24-88), ii) myelin loss and iron accumulation (N=92,age21-94), and iii) CBF deficits and iron accumulation (N=35,age22-88) in critical brain structures. This work may lay the foundation for further investigations of age-related WM degeneration and markers to differentiate normal from abnormal alterations. |
format | Online Article Text |
id | pubmed-7743490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77434902020-12-21 Cerebral Microstructure in Aging Using Advanced Quantitative MRI Bouhrara, Mustapha Khattar, Nikkita Kim, Richard Qian, Wenshu Alisch, Joseph Ferrucci, Luigi Resnick, Susan Spencer, Richard Innov Aging Abstracts White matter (WM) maintenance through oligodendrocyte metabolism is an energy-intensive process. Myelin homeostasis is sensitive to hypoxia, ischemia, or hypoperfusion. Besides substrate delivery, adequate cerebral blood flow (CBF) is crucial for removal of metabolic byproducts such as iron. While some data show decreased myelin content and CBF with aging, the association between CBF and myelination is unknown. Further, breakdown of oligodendrocyte and iron may potentiate myelin loss through oxidative mechanisms. Whether iron deposition is related to myelination is unclear. Using advanced MRI methodology, we investigated associations between CBF deficits, myelin loss, and iron deposition in cognitively normal individuals. We found significant association between i) CBF deficits and myelin loss (N=67,age24-88), ii) myelin loss and iron accumulation (N=92,age21-94), and iii) CBF deficits and iron accumulation (N=35,age22-88) in critical brain structures. This work may lay the foundation for further investigations of age-related WM degeneration and markers to differentiate normal from abnormal alterations. Oxford University Press 2020-12-16 /pmc/articles/PMC7743490/ http://dx.doi.org/10.1093/geroni/igaa057.2771 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstracts Bouhrara, Mustapha Khattar, Nikkita Kim, Richard Qian, Wenshu Alisch, Joseph Ferrucci, Luigi Resnick, Susan Spencer, Richard Cerebral Microstructure in Aging Using Advanced Quantitative MRI |
title | Cerebral Microstructure in Aging Using Advanced Quantitative MRI |
title_full | Cerebral Microstructure in Aging Using Advanced Quantitative MRI |
title_fullStr | Cerebral Microstructure in Aging Using Advanced Quantitative MRI |
title_full_unstemmed | Cerebral Microstructure in Aging Using Advanced Quantitative MRI |
title_short | Cerebral Microstructure in Aging Using Advanced Quantitative MRI |
title_sort | cerebral microstructure in aging using advanced quantitative mri |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743490/ http://dx.doi.org/10.1093/geroni/igaa057.2771 |
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