Search bioRxiv⌕ Search

Biology subjects

Wischnewski, K. J.

Publications and source records attributed to Wischnewski, K. J..

2 recordsLinked to original sources

cuBNM: GPU-Accelerated Brain Network Modeling

Brain network modeling uses computer simulations to infer about latent neural properties at micro- and mesoscales by fitting brain dynamic models to empirical data of individual subjects or groups. However, computational costs of (individualized) model fitting is a major bottleneck, limiting the practical feasibility of this approach to larger cohorts and more complex models, and highlighting the need for scalable simulation implementations. Here, we introduce cuBNM, a Python package which leverages parallel processing of graphics processing units to massively accelerate simulations of brain network models. We show running simulations on graphics processing units is several hundred times faster compared to central processing units. We demonstrate the usage of cuBNM by running optimization of group-level and individualized low- and high-dimensional models. As examples of the utility of individualized models, we investigated test-retest reliability and heritability of simulated and empirical measures in the Human Connectome Project dataset. We found simulated features were fairly reliable and significantly heritable, suggesting their biological plausibility. Overall, cuBNM enables large-scale simulations of brain network models, opening new avenues for studying latent neural processes across diverse populations, dense networks, and high-dimensional models, which was previously impractical due to computational constraints.

neuroscience↗

Adolescent maturation of cortical excitation-inhibition balance based on individualized biophysical network modeling

The balance of excitation and inhibition is a key functional property of cortical microcircuits which changes through the lifespan. Adolescence is considered a crucial period for the maturation of excitation-inhibition balance. This has been primarily observed in animal studies, yet human in vivo evidence on adolescent maturation of the excitation-inhibition balance at the individual level is limited. Here, we developed an individualized in vivo marker of regional excitation-inhibition balance in human adolescents, estimated using large-scale simulations of biophysical network models fitted to resting-state functional magnetic resonance imaging data from two independent cross-sectional (N = 752) and longitudinal (N = 149) cohorts. We found a widespread relative increase of inhibition in association cortices paralleled by a relative age-related increase of excitation, or lack of change, in sensorimotor areas across both datasets. This developmental pattern co-aligned with multiscale markers of sensorimotor-association differentiation. The spatial pattern of excitation-inhibition development in adolescence was robust to inter-individual variability of structural connectomes and modeling configurations. Notably, we found that alternative simulation-based markers of excitation-inhibition balance show a variable sensitivity to maturational change. Taken together, our study highlights an increase of inhibition during adolescence in association areas using cross sectional and longitudinal data, and provides a robust computational framework to estimate microcircuit maturation in vivo at the individual level.

neuroscience↗