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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
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.
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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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