# Brain-wide functional connectome analysis of 40,000 individuals reveals brain networks that show aging effects in older adults

**Authors:** Yezhi Pan, Chuan Bi, Peter Kochunov, Michelle Shardell, J. Carson Smith, Rozalina G. McCoy, Zhenyao Ye, Jiaao Yu, Tong Lu, Yifan Yang, Hwiyoung Lee, Song Liu, Si Gao, Yizhou Ma, Yiran Li, Chixiang Chen, Tianzhou Ma, Ze Wang, Thomas Nichols, L. Elliot Hong, Shuo Chen

PMC · DOI: 10.1162/imag_a_00394 · Imaging Neuroscience · 2024-12-16

## TL;DR

This study analyzed brain connectivity in 40,000 people and found two motor-related brain networks that decline with age, linked to white matter changes.

## Contribution

The study identifies specific brain subnetworks affected by aging and quantifies the role of white matter changes in these effects.

## Key findings

- Two motor-related subnetworks showed decreased resting-state functional connectivity with age.
- White matter fractional anisotropy mediates a significant portion of age-related connectivity decline.
- White matter hyperintensity volume also contributes to the aging-related decline in one subnetwork.

## Abstract

The functional connectome changes with aging. We systematically evaluated aging-related alterations in the functional connectome using a whole-brain connectome network analysis in 39,675 participants in UK Biobank project. We used adaptive dense network discovery tools to identify networks directly associated with aging from resting-state functional magnetic resonance imaging (fMRI) data. We replicated our findings in 499 participants from the Lifespan Human Connectome Project in Aging study. The results consistently revealed two motor-related subnetworks (both with permutation test p-values <0.001) that showed a decline in resting-state functional connectivity (rsFC) with increasing age. The first network primarily comprises sensorimotor and dorsal/ventral attention regions from precentral gyrus, postcentral gyrus, superior temporal gyrus, and insular gyrus, while the second network is exclusively composed of basal ganglia regions, namely the caudate, putamen, and globus pallidus. Path analysis indicates that white matter fractional anisotropy mediates 19.6% (p < 0.001, 95% CI [7.6% 36.0%]) and 11.5% (p < 0.001, 95% CI [6.3% 17.0%]) of the age-related decrease in both networks, respectively. The total volume of white matter hyperintensity mediates 32.1% (p < 0.001, 95% CI [16.8% 53.0%]) of the aging-related effect on rsFC in the first subnetwork.

## Full-text entities

- **Diseases:** white matter hyperintensity (MESH:D056784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12315726/full.md

## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC12315726/full.md

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Source: https://tomesphere.com/paper/PMC12315726