Biology subjects

Ashourvan, A.

Publications and source records attributed to Ashourvan, A..

13 recordsLinked to original sources

bioRxiv2025

A Concept-Driven Disentanglement Framework for Interpretable Graph Neural Networks in Structure-Function Coupling

Graph Neural Networks (GNNs) achieve state-of-the-art performance in predicting brain functional connectivity (FC) from structural connectivity (SC), yet their "black-box" nature limits interpretability and scientific utility. We present a concept-driven disentanglement framework that builds inherently interpretable GNNs for quantitative hypothesis testing of structure-function relationships. The framework employs an ensemble of GNN branches, each architecturally biased to learn from a predefined structural concept (e.g., strong vs. weak connections) by processing a filtered version of the SC graph. This design enforces verifiably disentangled node embeddings, ensuring each branch captures a distinct structural feature. Using SHAP (Shapley additive explanations), we quantify the predictive contribution of each concept and assess its statistical significance against null distributions. Our framework demonstrates high predictive accuracy for FC, achieving a group-level correlation coefficient of 0.91 on a public human connectome dataset, while simultaneously yielding interpretable neuroscientific insights. This interpretable-by-design methodology bridges the gap between predictive power and scientific transparency, enabling deep learning models to provide mechanistic insights into the brains network organization.

neuroscience↗

bioRxiv2024

Epileptiform activity and seizure risk follow long-term non-linear attractor dynamics

Many biological systems display circadian and slow multi-day rhythms, such as hormonal and cardiac cycles. In patients with epilepsy, these cycles also manifest as slow cyclical fluctuations in seizure propensity. However, such fluctuations in symptoms are consequences of the complex interactions between the underlying physiological, pathophysiological, and external causes. Therefore, identifying an accurate model of the underlying system that governs the multi-day rhythms allows for a more reliable seizure risk forecast and targeted interventions. To achieve this goal, we adopt the Hankel alternative view of Koopman (HAVOK) analysis to approximate a linear representation of nonlinear seizure propensity dynamics. The HAVOK framework leverages Koopman theory and delay-embedding to decompose chaotic dynamics into a linear system of leading delay-embedded coordinates driven by the low-energy coordinate (i.e., forcing). Our findings reveal the topology of attractors underlying multi-day seizure cycles, showing that seizures tend to occur in regions of the manifold with strongly nonlinear dynamics. Moreover, we demonstrate that the identified system driven by forcings with short periods up to a few days accurately predicts patients slower multi-day rhythms, which improves seizure risk forecasting.

neuroscience↗

bioRxiv2022

Development of Top-Down Cortical Propagations in Youth

Hierarchical processing requires activity propagating between higher and lower-order cortical areas. However, studies of brain development have chiefly quantified fluctuations within regions over time rather than propagations occurring over space. Here, we leveraged advances in neuroimaging and computer vision to track cortical activity propagations in a large sample of youth (n=388). We found that propagations robustly ascend and descend the cortical hierarchy, and that top-down propagations become both more prevalent with cognitive control demands and with development in youth.

neuroscience↗

bioRxiv2022

Thermal Effects on Neurons During Stimulation of the Brain

All artificial stimulation of the brain deposits thermal energy in the brain. This occurs through either Joule heating of the conductors carrying current through electrodes and magnetic coils, or through dissipation of energy in the conductive brain. Similarly, temperature affects all biological processes and chemical reactions. Although electrical interaction with brain tissue is inseparable from thermal effects when electrodes are used, magnetic induction enables us to separate Joule heating from induction effects by contrasting AC and DC driving of magnetic coils using the same energy deposition within the conductors. Since mammalian cortical neurons have no known sensitivity to static magnetic fields, and if there is no evidence of effect on spike timing to oscillating magnetic fields, we can presume that the induced electrical currents within the brain are below the molecular shot noise where any interaction with tissue is purely thermal. In this study, we examined a range of frequencies produced from micromagnetic coils operating below the molecular shot noise threshold for electrical interaction with single neurons. We found that small temperature increases and decreases of 1{degrees}C caused consistent transient suppression and excitation of neurons during temperature change. Numerical modeling of the biophysics demonstrated that the Na-K pump, and to a lesser extent the Nernst potential, could account for these transient effects. Such effects are dependent upon compartmental ion fluxes, and the rate of temperature change. A new bifurcation is described in the model dynamics that accounts for the transient suppression and excitation; in addition, we note the remarkable similarity of this bifurcations rate dependency with other thermal rate-dependent tipping points in planetary warming dynamics. Furthermore, bifurcations in the steady state dynamics leading to stable firing suppression are described for slightly higher temperatures. These experimental and theoretical findings demonstrate that stimulation of the brain must take into account small thermal effects that are ubiquitously present in electrical and magnetic stimulation. More sophisticated models of electrical current interaction with neurons combined with thermal effects will be required in order to more accurately enable model-based control of neuronal circuitry.

biophysics↗

bioRxiv2021

External drivers of BOLD signals non-stationarity

A fundamental challenge in neuroscience is to uncover the principles governing how the brain interacts with the external environment. However, assumptions about external stimuli fundamentally constrain current computational models. We show in silico that unknown external stimulation can produce error in the estimated linear time-invariant dynamical system. To address these limitations, we propose an approach to retrieve the external (unknown) input parameters and demonstrate that the estimated system parameters during external input quiescence uncover spatiotemporal profiles of external inputs over external stimulation periods more accurately. Finally, we unveil the expected (and unexpected) sensory and task-related extra-cortical input profiles using functional magnetic resonance imaging data acquired from 96 subjects (Human Connectome Project) during the resting-state and task scans. Together, we provide evidence that this embodied brain activity model offers information about the structure and dimensionality of the BOLD signals external drivers and shines light on likely external sources contributing to the BOLD signals non-stationarity.

neuroscience↗

bioRxiv2020

Multimodal in vivo recording using transparent graphene microelectrodes illuminates spatiotemporal seizure dynamics at the microscale

Neurological disorders such as epilepsy arise from disrupted brain networks. Our capacity to treat these disorders is limited by our inability to map these networks at sufficient temporal and spatial scales to target interventions. Current best techniques either sample broad areas at low temporal resolution (e.g. calcium imaging) or record from discrete regions at high temporal resolution (e.g. electrophysiology). This limitation hampers our ability to understand and intervene in aberrations of network dynamics. Here we present a technique to map the onset and spatiotemporal spread of acute epileptic seizures in vivo by simultaneously recording high bandwidth microelectrocorticography and calcium fluorescence using transparent graphene microelectrode arrays. We integrate dynamic data features from both modalities using non-negative matrix factorization to identify sequential spatiotemporal patterns of seizure onset and evolution, revealing how the temporal progression of ictal electrophysiology is linked to the spatial evolution of the recruited seizure core. This integrated analysis of multimodal data reveals otherwise hidden state transitions in the spatial and temporal progression of acute seizures. The techniques demonstrated here may enable future targeted therapeutic interventions and novel spatially embedded models of local circuit dynamics during seizure onset and evolution.

neuroscience↗

bioRxiv2019

A dynamical systems framework to uncover the drivers of large-scale cortical activity

A fundamental challenge in neuroscience is to uncover the principles governing complex interactions between the brain and its external environment. Over the past few decades, the development of functional neuroimaging techniques and tools from graph theory, network science, and computational neuroscience have markedly expanded opportunities to study the intrinsic organization of brain activity. However, many current computational models are fundamentally limited by little to no explicit assessment of the brains interactions with external stimuli. To address this limitation, we propose a simple scheme that jointly estimates the intrinsic organization of brain activity and extrinsic stimuli. Specifically, we adopt a linear dynamical model (intrinsic activity) under unknown exogenous inputs (e.g., sensory stimuli), and jointly estimate the model parameters and exogenous inputs. First, we demonstrate the utility of this scheme by accurately estimating unknown external stimuli in a synthetic example. Next, we examine brain activity at rest and task for 99 subjects from the Human Connectome Project, and find significant task-related changes in the identified system, and task-related increases in the estimated external inputs showing high similarity to known task regressors. Finally, through detailed examination of fluctuations in the spatial distribution of the oscillatory modes of the estimated system during the resting state, we find an apparent non-stationarity in the profile of modes that span several brain regions including the visual and the dorsal attention systems. The results suggest that these brain structures display a time-varying relationship, or alternatively, receive non-stationary exogenous inputs that can lead to apparent system non-stationarities. Together, our embodied model of brain activity provides an avenue to gain deeper insight into the relationship between cortical functional dynamics and their drivers.

neuroscience↗

bioRxiv2018

A pairwise maximum entropy model uncovers the white matter scaffold underlying emergent dynamics in intracranial EEG

A major challenge in systems neuroscience is to understand how the brains structural architecture gives rise to its complex functional dynamics. Here, we address this challenge by examining the inter-ictal activity of five patients with medically refractory epilepsy during [~] 15 hours of multi-channel intracranial recording. By constructing a pairwise maximum entropy model (MEM) of the observed neural dynamics, we seek to uncover the fundamental relationship between functional activity and its underlying structural substrate. Despite only incorporating the pairwise correlations in the observed neural activity, we find that the pairwise MEM robustly fits large-scale patterns of inter-ictal power dynamics across a wide range of frequency bands, notably displaying time-invariance and cross-frequency similarity. Furthermore, across all frequency bands, we demonstrate that the pairwise MEM accurately identifies the structural white matter connections between brain regions, outperforming other common model-free measures of functional connectivity. Together, our findings show that a simple pairwise MEM, which is explicitly ignorant of higher-order correlations between three or more brain regions, not only captures complex spatiotemporal patterns of neural activity across the frequency spectrum, but also suggests that the network of structural connections in the human brain is a plausible scaffold capable of supporting observed wide-band neural dynamics.

neuroscience↗

bioRxiv2018

Reconfigurations within resonating communities of brain regions following TMS reveal different scales of processing

1An overarching goal of neuroscience research is to understand how heterogeneous neuronal ensembles cohere into networks of coordinated activity to support cognition. To investigate how local activity harmonizes with global signals, we measured electroencephalography (EEG) while single pulses of transcranial magnetic stimulation (TMS) perturbed occipital and parietal cortices. We estimate the rapid network reconfigurations in dynamic network communities within specific frequency bands of the EEG, and characterize two distinct features of network reconfiguration, flexibility and allegiance, among spatially distributed neural sources following TMS. Using distance from the stimulation site to infer local and global effects, we find that alpha activity (8-12Hz) reflects concurrent local and global effects on network dynamics. Pair-wise allegiance of brain regions to communities on average increased near the stimulation site, whereas TMS-induced changes to flexibility were generally invariant to distance and stimulation site. In contrast, communities within the beta (13-20Hz) band demonstrated a high level of spatial specificity, particularly within a cluster comprising paracentral areas. Together, these results suggest that focal magnetic neurostimulation to distinct cortical sites can help identify both local and global effects on brain network dynamics, and highlight fundamental differences in the manifestation of network reconfigurations within alpha and beta frequency bands. 2 Author SummaryTMS may be used to probe the causal link between local regional activity and global brain dynamics. Using simultaneous TMS-EEG and dynamic community detection, we introduce what we call "resonating clusters", or frequency band-specific communities in the brain, as a way to index local and global processing. These resonating clusters within the alpha and beta bands brain display both global (or integrating) behavior and local specificity, highlighting fundamental differences in the manifestation of network reconfigurations.

neuroscience↗

bioRxiv2018

High interictal connectivity within the resection zone is associated with favorable post-surgical outcomes in focal epilepsy patients

ObjectivePatients with drug-resistant focal epilepsy are often candidates for invasive surgical therapies. In these patients, it is necessary to accurately localize seizure-generators to ensure seizure freedom following intervention. While intracranial electroencephalography (iEEG) is the gold standard for mapping networks for surgery, this approach requires inducing and recording seizures, which may cause patient morbidity. The goal of this study is to evaluate the utility of mapping interictal (non-seizure) iEEG networks to identify targets for surgical treatment.\n\nMethodsWe analyze interictal iEEG recordings and neuroimaging from 27 focal epilepsy patients treated via surgical resection. We generate interictal functional networks by calculating pairwise correlation of iEEG signals across different frequency bands. We identify electrodes falling within surgically resected tissue (i.e. the resection zone), and compute node-level and edge-level synchrony in relation to the resection zone. We associate these metrics with post-surgical outcomes.\n\nResultsGreater overlap between resected electrodes and highly synchronous electrodes is associated with favorable post-surgical outcomes. Additionally, good outcome patients have significantly higher connectivity localized within the resection zone compared to those with poorer postoperative seizure control. This finding persists following normalization by a spatially-constrained null model.\n\nConclusionsThis study suggests that spatially-informed interictal network synchrony measures can distinguish between good and poor post-surgical outcomes. By capturing clinically relevant information during interictal periods, our method may ultimately reduce the need for prolonged invasive implants and provide insights into the pathophysiology of an epileptic brain. We discuss next steps for translating these findings into a prospectively useful clinical tool.

neuroscience↗

bioRxiv2018

Context-dependent architecture of brain state dynamics is explained by white matter connectivity and theories of network control

A diverse white matter network and finely tuned neuronal membrane properties allow the brain to transition seamlessly between cognitive states. However, it remains unclear how static structural connections guide the temporal progression of large-scale brain activity patterns in different cognitive states. Here, we deploy an unsupervised machine learning algorithm to define brain states as time point level activity patterns from functional magnetic resonance imaging data acquired during passive visual fixation (rest) and an n-back working memory task. We find that brain states are composed of interdigitated functional networks and exhibit context-dependent dynamics. Using diffusion-weighted imaging acquired from the same subjects, we show that structural connectivity constrains the temporal progression of brain states. We also combine tools from network control theory with geometrically conservative null models to demonstrate that brains are wired to support states of high activity in default mode areas, while requiring relatively low energy. Finally, we show that brain state dynamics change throughout development and explain working memory performance. Overall, these results elucidate the structural underpinnings of cognitively and developmentally relevant spatiotemporal brain dynamics.

neuroscience↗

bioRxiv2018

Local structural connectivity directs seizure spread in focal epilepsy

How does the human brains structural scaffold give rise to its intricate functional dynamics? This is a central challenge in translational neuroscience, particularly in epilepsy, a disorder that affects over 50 million people worldwide. Treatment for medication-resistant focal epilepsy is often structural - through surgery, devices or focal laser ablation - but structural targets, particularly in patients without clear lesions, are largely based on functional mapping via intracranial EEG (iEEG). Unfortunately, the relationship between structural and functional connectivity in the seizing brain is poorly understood. In this study, we quantify structure-function coupling, specifically between white matter connections and iEEG, across preictal and ictal periods in 45 seizures from 9 patients with unilateral drug-resistant focal epilepsy. We use High Angular Resolution Diffusion Imaging (HARDI) tractography to construct structural connectivity networks and correlate these networks with time-varying broadband and frequency-specific functional networks derived from coregistered iEEG. Across all frequency bands, we find significant increases in structure-function coupling from preictal to ictal periods. We demonstrate that short-range structural connections are primarily responsible for this increase in coupling. Finally, we find that spatiotemporal patterns of structure-function coupling are stereotyped, and a function of each patients individual anatomy. These results suggest that seizures harness the underlying structural connectome as they propagate. Our findings suggest that the relationship between structural and functional connectivity in epilepsy may inform current and new therapies to map and alter seizure spread, and pave the way for better-targeted, patient-specific interventions.

neuroscience↗

bioRxiv2017

Applications of community detection techniques to brain graphs: Algorithmic considerations and implications for neural function

The human brain can be represented as a graph in which neural units such as cells or small volumes of tissue are heterogeneously connected to one another through structural or functional links. Brain graphs are parsimonious representations of neural systems that have begun to offer fundamental insights into healthy human cognition, as well as its alteration in disease. A critical open question in network neuroscience lies in how neural units cluster into densely interconnected groups that can provide the coordinated activity that is characteristic of perception, action, and adaptive behaviors. Tools that have proven particularly useful for addressing this question are community detection approaches, which can be used to identify communities or modules in brain graphs: groups of neural units that are densely interconnected with other units in their own group but sparsely interconnected with units in other groups. In this paper, we describe a common community detection algorithm known as modularity maximization, and we detail its applications to brain graphs constructed from neuroimaging data. We pay particular attention to important algorithmic considerations, especially in recent extensions of these techniques to graphs that evolve in time. After recounting a few fundamental insights that these techniques have provided into brain function, we highlight potential avenues of methodological advancements for future studies seeking to better characterize the patterns of coordinated activity in the brain that accompany human behavior. This tutorial provides a naive reader with an introduction to theoretical considerations pertinent to the generation of brain graphs, an understanding of modularity maximization for community detection, a resource of statistical measures that can be used to characterize community structure, and an appreciation of the utility of these approaches in uncovering behaviorally-relevant network dynamics in neuroimaging data.

neuroscience↗