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Abstract

The synchronized firing of distant neuronal populations gives rise to a wide array of functional brain networks that underlie human brain function. Given the enormous perception, learning, and cognition potential of the human brain, it is not surprising that network-level representations of brain function reveal intrinsically rich organizational structure. What remains puzzling is how the human brain maintains its vast repertoire of functional connectivity (FC) states despite being constrained by the underlying fixed anatomical substrate. Advances in modern neuroimaging technologies, such as diffusion-weighted magnetic resonance imaging (DW-MRI), have made it possible to map the brain's anatomical scaffold, while functional MRI (fMRI) provides complementary information on neural activity. In this thesis, we develop and apply methods for combining DW-MRI and fMRI data into an integrated framework to analyze the interplay between brain structure and function. We first explored the dynamics of brain function during wakefulness and across the different non-rapid eye movement (NREM) sleep stages. We applied the innovation-driven co-activation pattern (iCAP) analysis to uncover the spatial and temporal organization of overlapping large-scale brain networks. Our results reveal new spatial patterns covering regions that support the physiological organization of sleep and arousal. Contrary to the previously observed decreasing FC that accompanies increasing sleep depth, we instead observe a surge of network activity and cross-network interactions during NREM stage 2, followed by an abrupt decrease in NREM stage 3. In the next step of the thesis, we propose a new method that models all brain voxels as nodes of a high-resolution voxel-level brain graph. We provide two ways to construct the graph and we characterize their properties by performing a spectral analysis of the graph Laplacian operator. Our findings show that despite the huge dimensionality of the proposed brain graphs, the majority of the structural information is captured by the Laplacian's lowest frequency eigenmodes. The lower end of the Laplacian spectra also captures about 85% of the energy content of functional MRI, suggesting that functional patterns are overall smooth over the structure, thus providing, for the first time, a direct and quantitative measure of how much brain function is shaped by the anatomy. Going beyond a scalar measure of the SC-FC link, we introduce a new framework that interpolates gray matter signals onto the white matter using the structure embedded in the voxel-level brain grid to guide the process. This enables visualization of key white matter structures that link temporally coherent gray matter areas. We found whole-brain structure-function networks that extend currently known spatial patterns that are limited within the gray matter only. Finally, we assessed the collective mediation of white matter pathways by giving a quantitative measure of the overall anatomical range between temporally coherent gray matter areas. We utilized a canonical model of graph diffusion to extract the anatomical range of functional network interactions. We find that this measure meaningfully differentiates brain regions according to a behaviorally relevant macroscale gradient that divides the cortex between low-level primary sensory areas and high-level cognitive functions.

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