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Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects

Brain aging is a complex process that requires a multimodal approach. Neuroimaging can provide insights into brain morphology, functional organization, and vascular dynamics. However, most neuroimaging studies of aging have focused on each imaging modality separately, limiting the understanding of i...

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Autores principales: Liu, Xulin, Tyler, Lorraine K., Rowe, James B., Tsvetanov, Kamen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704789/
https://www.ncbi.nlm.nih.gov/pubmed/35855641
http://dx.doi.org/10.1002/hbm.26025
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author Liu, Xulin
Tyler, Lorraine K.
Rowe, James B.
Tsvetanov, Kamen A.
author_facet Liu, Xulin
Tyler, Lorraine K.
Rowe, James B.
Tsvetanov, Kamen A.
author_sort Liu, Xulin
collection PubMed
description Brain aging is a complex process that requires a multimodal approach. Neuroimaging can provide insights into brain morphology, functional organization, and vascular dynamics. However, most neuroimaging studies of aging have focused on each imaging modality separately, limiting the understanding of interrelations between processes identified by different modalities and their relevance to cognitive decline in aging. Here, we used a data‐driven multimodal approach, linked independent component analysis (ICA), to jointly analyze magnetic resonance imaging (MRI) of grey matter volume, cerebrovascular, and functional network topographies in relation to measures of fluid intelligence. Neuroimaging and cognitive data from the Cambridge Centre for Ageing and Neuroscience study were used, with healthy participants aged 18–88 years (main dataset n = 215 and secondary dataset n = 433). Using linked ICA, functional network activities were characterized in independent components but not captured in the same component as structural and cerebrovascular patterns. Split‐sample (n = 108/107) and out‐of‐sample (n = 433) validation analyses using linked ICA were also performed. Global grey matter volume with regional cerebrovascular changes and the right frontoparietal network activity were correlated with age‐related and individual differences in fluid intelligence. This study presents the insights from linked ICA to bring together measurements from multiple imaging modalities, with independent and additive information. We propose that integrating multiple neuroimaging modalities allows better characterization of brain pattern variability and changes associated with healthy aging.
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spelling pubmed-97047892022-11-29 Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects Liu, Xulin Tyler, Lorraine K. Rowe, James B. Tsvetanov, Kamen A. Hum Brain Mapp Research Articles Brain aging is a complex process that requires a multimodal approach. Neuroimaging can provide insights into brain morphology, functional organization, and vascular dynamics. However, most neuroimaging studies of aging have focused on each imaging modality separately, limiting the understanding of interrelations between processes identified by different modalities and their relevance to cognitive decline in aging. Here, we used a data‐driven multimodal approach, linked independent component analysis (ICA), to jointly analyze magnetic resonance imaging (MRI) of grey matter volume, cerebrovascular, and functional network topographies in relation to measures of fluid intelligence. Neuroimaging and cognitive data from the Cambridge Centre for Ageing and Neuroscience study were used, with healthy participants aged 18–88 years (main dataset n = 215 and secondary dataset n = 433). Using linked ICA, functional network activities were characterized in independent components but not captured in the same component as structural and cerebrovascular patterns. Split‐sample (n = 108/107) and out‐of‐sample (n = 433) validation analyses using linked ICA were also performed. Global grey matter volume with regional cerebrovascular changes and the right frontoparietal network activity were correlated with age‐related and individual differences in fluid intelligence. This study presents the insights from linked ICA to bring together measurements from multiple imaging modalities, with independent and additive information. We propose that integrating multiple neuroimaging modalities allows better characterization of brain pattern variability and changes associated with healthy aging. John Wiley & Sons, Inc. 2022-07-20 /pmc/articles/PMC9704789/ /pubmed/35855641 http://dx.doi.org/10.1002/hbm.26025 Text en © 2022 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
Liu, Xulin
Tyler, Lorraine K.
Rowe, James B.
Tsvetanov, Kamen A.
Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
title Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
title_full Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
title_fullStr Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
title_full_unstemmed Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
title_short Multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
title_sort multimodal fusion analysis of functional, cerebrovascular and structural neuroimaging in healthy aging subjects
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704789/
https://www.ncbi.nlm.nih.gov/pubmed/35855641
http://dx.doi.org/10.1002/hbm.26025
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