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David Roalf

Publications and source records attributed to David Roalf.

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Developmental increases in white matter network controllability support a growing diversity of brain dynamics

As the human brain develops, it increasingly supports coordinated control of neural activity. The mechanism by which white matter evolves to support this coordination is not well understood. We use a network representation of diffusion imaging data from 882 youth ages 8 to 22 to show that white matter connectivity becomes increasingly optimized for a diverse range of predicted dynamics in development. Notably, stable controllers in subcortical areas are negatively related to cognitive performance. Investigating structural mechanisms supporting these changes, we simulate network evolution with a set of growth rules. We find that all brain networks are structured in a manner highly optimized for network control, with distinct control mechanisms predicted in child versus older youth. We demonstrate that our results cannot be simply explained by changes in network modularity. This work reveals a possible mechanism of human brain development that preferentially optimizes dynamic network control over static network architecture.

q-bio.NC

The modular organization of human anatomical brain networks: Accounting for the cost of wiring

Brain networks are expected to be modular. However, existing techniques for estimating a network's modules make it difficult to assess the influence of organizational principles such as wiring cost reduction on the detected modules. Here, we present a modification of an existing module detection algorithm that allows us to focus on connections that are unexpected under a cost-reduction wiring rule and to identify modules from among these connections. We apply this technique to anatomical brain networks and show that the modules we detect differ from those detected using the standard technique. We demonstrate that these novel modules are spatially distributed, exhibit unique functional fingerprints, and overlap considerably with rich clubs, giving rise to an alternative and complementary interpretation of the functional roles of specific brain regions. Finally, we demonstrate that, using the modified module detection approach, we can detect modules in a developmental dataset that track normative patterns of maturation. Collectively, these findings support the hypothesis that brain networks are composed of modules and provide additional insight into the function of those modules.

q-bio.NC