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Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness

View ORCID ProfileChristina Stier, View ORCID ProfileChristoph Braun, View ORCID ProfileNiels K. Focke
doi: https://doi.org/10.1101/2022.10.23.513274
Christina Stier
1Clinic of Neurology, University Medical Center Göttingen, Göttingen, Germany
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  • For correspondence: christina.stier@med.uni-goettingen.de nfocke@uni-goettingen.de
Christoph Braun
2MEG-Center, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
3CIMeC, Center for Mind/Brain Sciences, University of Trento, Rovereto, Italy
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Niels K. Focke
1Clinic of Neurology, University Medical Center Göttingen, Göttingen, Germany
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  • ORCID record for Niels K. Focke
  • For correspondence: christina.stier@med.uni-goettingen.de nfocke@uni-goettingen.de
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Abstract

Oscillatory power and phase synchronization map neuronal dynamics and are commonly studied to describe the healthy or diseased human brain. Yet, little is known about the course 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 of age effects on cortical thickness and those on functional networks and a direct relationship at the level of the study sample. We found MEG frequency-specific patterns for lower- and higher-order brain regions and divergence between sexes in low frequencies. Connectivity and power exhibited distinct linear trajectories with age or turning points at midlife, which in the delta and beta bands corresponded to the age patterns of cortical thickness. Structure-function coupling was frequency-dependent and observed in unimodal or transmodal 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.

Competing Interest Statement

N.K. Focke has received speaker bureau and consultancy fees from Arvelle/Angelini, Bial, and Eisai, all unrelated to the present project. C. Stier and C. Braun have no relevant financial or non-financial interests to disclose.

Footnotes

  • Minor revision of the abstract, re-formatting of references

  • https://github.com/chstier/Lifespan_MEG

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted December 03, 2022.
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Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness
Christina Stier, Christoph Braun, Niels K. Focke
bioRxiv 2022.10.23.513274; doi: https://doi.org/10.1101/2022.10.23.513274
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Adult lifespan trajectories of neuromagnetic signals and interrelations with cortical thickness
Christina Stier, Christoph Braun, Niels K. Focke
bioRxiv 2022.10.23.513274; doi: https://doi.org/10.1101/2022.10.23.513274

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