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Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing
Unveiling the details of white matter (WM) maturation throughout ageing is a fundamental question for understanding the ageing brain. In an extensive comparison of brain age predictions and age‐associations of WM features from different diffusion approaches, we analyzed UK Biobank diffusion magnetic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258541/ https://www.ncbi.nlm.nih.gov/pubmed/37195079 http://dx.doi.org/10.1002/hbm.26333 |
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author | Korbmacher, Max de Lange, Ann Marie van der Meer, Dennis Beck, Dani Eikefjord, Eli Lundervold, Arvid Andreassen, Ole A. Westlye, Lars T. Maximov, Ivan I. |
author_facet | Korbmacher, Max de Lange, Ann Marie van der Meer, Dennis Beck, Dani Eikefjord, Eli Lundervold, Arvid Andreassen, Ole A. Westlye, Lars T. Maximov, Ivan I. |
author_sort | Korbmacher, Max |
collection | PubMed |
description | Unveiling the details of white matter (WM) maturation throughout ageing is a fundamental question for understanding the ageing brain. In an extensive comparison of brain age predictions and age‐associations of WM features from different diffusion approaches, we analyzed UK Biobank diffusion magnetic resonance imaging (dMRI) data across midlife and older age (N = 35,749, 44.6–82.8 years of age). Conventional and advanced dMRI approaches were consistent in predicting brain age. WM‐age associations indicate a steady microstructure degeneration with increasing age from midlife to older ages. Brain age was estimated best when combining diffusion approaches, showing different aspects of WM contributing to brain age. Fornix was found as the central region for brain age predictions across diffusion approaches in complement to forceps minor as another important region. These regions exhibited a general pattern of positive associations with age for intra axonal water fractions, axial, radial diffusivities, and negative relationships with age for mean diffusivities, fractional anisotropy, kurtosis. We encourage the application of multiple dMRI approaches for detailed insights into WM, and the further investigation of fornix and forceps as potential biomarkers of brain age and ageing. |
format | Online Article Text |
id | pubmed-10258541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102585412023-06-13 Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing Korbmacher, Max de Lange, Ann Marie van der Meer, Dennis Beck, Dani Eikefjord, Eli Lundervold, Arvid Andreassen, Ole A. Westlye, Lars T. Maximov, Ivan I. Hum Brain Mapp Research Articles Unveiling the details of white matter (WM) maturation throughout ageing is a fundamental question for understanding the ageing brain. In an extensive comparison of brain age predictions and age‐associations of WM features from different diffusion approaches, we analyzed UK Biobank diffusion magnetic resonance imaging (dMRI) data across midlife and older age (N = 35,749, 44.6–82.8 years of age). Conventional and advanced dMRI approaches were consistent in predicting brain age. WM‐age associations indicate a steady microstructure degeneration with increasing age from midlife to older ages. Brain age was estimated best when combining diffusion approaches, showing different aspects of WM contributing to brain age. Fornix was found as the central region for brain age predictions across diffusion approaches in complement to forceps minor as another important region. These regions exhibited a general pattern of positive associations with age for intra axonal water fractions, axial, radial diffusivities, and negative relationships with age for mean diffusivities, fractional anisotropy, kurtosis. We encourage the application of multiple dMRI approaches for detailed insights into WM, and the further investigation of fornix and forceps as potential biomarkers of brain age and ageing. John Wiley & Sons, Inc. 2023-05-17 /pmc/articles/PMC10258541/ /pubmed/37195079 http://dx.doi.org/10.1002/hbm.26333 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Korbmacher, Max de Lange, Ann Marie van der Meer, Dennis Beck, Dani Eikefjord, Eli Lundervold, Arvid Andreassen, Ole A. Westlye, Lars T. Maximov, Ivan I. Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
title | Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
title_full | Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
title_fullStr | Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
title_full_unstemmed | Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
title_short | Brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
title_sort | brain‐wide associations between white matter and age highlight the role of fornix microstructure in brain ageing |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258541/ https://www.ncbi.nlm.nih.gov/pubmed/37195079 http://dx.doi.org/10.1002/hbm.26333 |
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