bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.04.17.649421

Small-world scale-free brain graphs from EEG

Abstract

Developing individualized spatial models that capture the complex dynamics of multi-electrode EEG data is essential for accurately decoding global neural activity. A widely used approach is network modeling, where electrodes are represented as nodes. A key challenge lies in defining the network edges and weights, as precise connectivity estimation is critical for enhancing neural characterization and extracting discriminative features, such as those needed for task decoding. Traditional EEG-derived brain graphs often fail to capture biologically grounded organizational principles such as small-world structure and heavy-tailed (scale-free) connectivity patterns. To address this gap, we introduce a framework for inferring subject-specific EEG-based brain graphs that explicitly designed to exhibit small-world and scale-free properties. Our approach begins by computing phase-locking values (PLV) between EEG channel pairs to build a backbone graph, which is then refined into an individualized small-world and scale-free network. To reduce computational complexity while preserving subject-specific characteristics, we apply Kron reduction to the resulting graph. Using two public EEG datasets, we evaluate the proposed method on motor imagery (MI) decoding and brain fingerprinting tasks. Our approach improves MI classification accuracy by 4-7% compared to conventional PLV, small-world, and scale-free graph models, and enhances differential identifiability in fingerprinting by 8-20% across six canonical frequency bands. These gains were statistically significant in both applications. Moreover, integrating graph signal processing features derived from our constructed graphs with classical EEG features further boosts performance. Overall, our findings highlight the potential of the proposed graph construction framework to enhance EEG analysis. By jointly capturing local segregation, global integration, and hub-driven hierarchical organization, the method strengthens downstream decoding and identification tasks, with promising implications for a wide range of applications in cognitive neuroscience and brain-computer interface research.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Khalili, M. D., Abootalebi, V., Saeedi-Sourck, H., Santoro, A., Behjat, H. H.. 2025-04-23. Small-world scale-free brain graphs from EEG. https://doi.org/10.1101/2025.04.17.649421

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Rab10 and Arhgef7 interact to promote axon extension by linking vesicle supply and exocytosis

The formation of functional neural circuits begins with the extension of a single axon by immature neurons. Axon elongation requires an expansion of the plasma membrane that depends on the polarization of vesicle trafficking and exocytosis. It is not completely understood how the increased transport of vesicles into the growing axon is linked to their subsequent insertion into the plasma membrane. An analysis of early stages of neuronal differentiation indicates that an asymmetry in neurite length precedes axon specification and the accumulation of PPVs in the nascent axon. We show that increasing the transport of vesicles in unpolarized neurons is sufficient to promote the extension of additional axons. This effect indicates that an increased supply of vesicles stimulates their subsequent insertion into the membrane to allow neurite growth. The link between vesicle transport and exocytosis is mediated by the interaction of Rab10 with Arhgef7. Rab10 stimulates Arhgef7 activity on PPVs as a GEF for Cdc42b to promote axon extension through exocyst-dependent exocytosis, suggesting that their interaction links the increased supply of PPVs to their exocytosis.

neuroscience↗

Subcellular Spatial Profiling Unveils Links Between Neuritic Plaques with Selective Tau Vulnerability in Alzheimer's Disease

Alzheimer's disease (AD) features widespread extracellular amyloid-{beta} plaques but selective intraneuronal tau accumulation in cortical layers II/III and V, while layer IV remains relatively resistant. Here, we combined subcellular spatial transcriptomics with co-registered A{beta} and pTau immunohistochemistry to determine why neurons exposed to comparable plaque-associated pathology differ in somatic pTau accumulation. Plaque-associated neuritic stress occurred similarly across layers, but layer IV neurons showed attenuated pTau accumulation and reduced somatic expression of a shared neurite-soma stress program involving DCTN1, CALM3, NORAD, and PIN1. Trajectory analysis within layers identified tau-vulnerable and resistant neuronal states implicating calcium signaling, retrograde transport, and lysosomal function. Notably, astrocytic APOE-neuronal LRP1 co-expression increased significantly along the pTau-vulnerable trajectory, and APOE {epsilon}4 was associated with stronger coupling of local plaque pathology to pTau-associated molecular programs. These findings reveal neuronal programs and neuron-glia interactions underlying selective tau vulnerability and resistance in AD, highlighting potential tau-targeting therapeutics.

neuroscience↗

Widespread oscillatory suppression in autism persists in the absence of psychotropic medication.

Purpose: Investigate the neural oscillatory activity associated with autism spectrum disorder (ASD) using electroencephalographic (EEG) recordings in children and adolescents. Compare the corresponding oscillatory power between ASD patients taking psychotropic medication with a drug-naive group. Methods: ASD diagnosis was done using DSM-IV and CARS (Childhood Autism Rating Scale). EEG recordings employed 22 scalp electrodes (10/20 system). ASD vs. neurotypical groups were matched for sex and age (5 females; average age: ~10 years old). We analyzed the resting state (eyes open) EEG power spectrum during ~2-minute recordings. The multitaper FFT method was used to estimate spectral power for the delta, theta, alpha, beta and gamma frequency bands. We pooled together data from several electrodes to compute comprehensive power spectra and assess the oscillatory behavior of macro brain regions. Results: We observed widespread (~4Hz - 20Hz) oscillatory suppression comprising the theta, alpha and beta frequency bands. The most widespread and robust ASD-associated power suppression was in the high theta and alpha bands. Delta and gamma bands showed no significant power change for any of the brain regions studied. Results from a subgroup of patients (N = 9) who never used psychotropics confirmed these findings, indicating that they are not an artifact of medication. Conclusion: Suppression in theta, alpha and beta oscillations may offer insights into the neurophysiological underpinnings of autism and could be used as an accessible and comprehensive tool in ASD diagnosis, regardless of the patients being or not on medication.

neuroscience↗