Cargando…
Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness
Oscillatory power and phase synchronization map neuronal dynamics and are commonly studied to differentiate the healthy and diseased brain. Yet, little is known about the course and spatial variability of these features from early adulthood into old age. Leveraging magnetoencephalography (MEG) resti...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443236/ https://www.ncbi.nlm.nih.gov/pubmed/37451375 http://dx.doi.org/10.1016/j.neuroimage.2023.120275 |
_version_ | 1785093779571605504 |
---|---|
author | Stier, Christina Braun, Christoph Focke, Niels K. |
author_facet | Stier, Christina Braun, Christoph Focke, Niels K. |
author_sort | Stier, Christina |
collection | PubMed |
description | Oscillatory power and phase synchronization map neuronal dynamics and are commonly studied to differentiate the healthy and diseased brain. Yet, little is known about the course and spatial variability of these features from early adulthood into old age. Leveraging magnetoencephalography (MEG) resting-state data in a cross-sectional adult sample (n = 350), we probed lifespan differences (18–88 years) in connectivity and power and interaction effects with sex. Building upon recent attempts to link brain structure and function, we tested the spatial correspondence between age effects on cortical thickness and those on functional networks. We further probed a direct structure-function relationship at the level of the study sample. We found MEG frequency-specific patterns with age and divergence between sexes in low frequencies. Connectivity and power exhibited distinct linear trajectories or turning points at midlife that might reflect different physiological processes. In the delta and beta bands, these age effects corresponded to those on cortical thickness, pointing to co-variation between the modalities across the lifespan. Structure-function coupling was frequency-dependent and observed in unimodal or multimodal regions. Altogether, we provide a comprehensive overview of the topographic functional profile of adulthood that can form a basis for neurocognitive and clinical investigations. This study further sheds new light on how the brain's structural architecture relates to fast oscillatory activity. |
format | Online Article Text |
id | pubmed-10443236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104432362023-09-01 Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness Stier, Christina Braun, Christoph Focke, Niels K. Neuroimage Article Oscillatory power and phase synchronization map neuronal dynamics and are commonly studied to differentiate the healthy and diseased brain. Yet, little is known about the course and spatial variability of these features from early adulthood into old age. Leveraging magnetoencephalography (MEG) resting-state data in a cross-sectional adult sample (n = 350), we probed lifespan differences (18–88 years) in connectivity and power and interaction effects with sex. Building upon recent attempts to link brain structure and function, we tested the spatial correspondence between age effects on cortical thickness and those on functional networks. We further probed a direct structure-function relationship at the level of the study sample. We found MEG frequency-specific patterns with age and divergence between sexes in low frequencies. Connectivity and power exhibited distinct linear trajectories or turning points at midlife that might reflect different physiological processes. In the delta and beta bands, these age effects corresponded to those on cortical thickness, pointing to co-variation between the modalities across the lifespan. Structure-function coupling was frequency-dependent and observed in unimodal or multimodal regions. Altogether, we provide a comprehensive overview of the topographic functional profile of adulthood that can form a basis for neurocognitive and clinical investigations. This study further sheds new light on how the brain's structural architecture relates to fast oscillatory activity. Academic Press 2023-09 /pmc/articles/PMC10443236/ /pubmed/37451375 http://dx.doi.org/10.1016/j.neuroimage.2023.120275 Text en © 2023 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Stier, Christina Braun, Christoph Focke, Niels K. Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
title | Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
title_full | Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
title_fullStr | Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
title_full_unstemmed | Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
title_short | Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
title_sort | adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443236/ https://www.ncbi.nlm.nih.gov/pubmed/37451375 http://dx.doi.org/10.1016/j.neuroimage.2023.120275 |
work_keys_str_mv | AT stierchristina adultlifespantrajectoriesofneuromagneticsignalsandinterrelationswithcorticalthickness AT braunchristoph adultlifespantrajectoriesofneuromagneticsignalsandinterrelationswithcorticalthickness AT fockenielsk adultlifespantrajectoriesofneuromagneticsignalsandinterrelationswithcorticalthickness |