Biology subjects

Agcaoglu, O.

Publications and source records attributed to Agcaoglu, O..

5 recordsLinked to original sources

bioRxiv2025

An information theory framework for capturing multi-connectivity via spatial network encoding reveals reduced population count (Hamming weight) localized to auditory, visual, and motor networks

1.The human brain operates as a complex system where functional networks evolve and interact across spatially distributed regions. In traditional neuroimaging analyses, functional connectivity (FC), based on pairwise correlations or statistical dependencies of temporal fluctuations in the BOLD signal, has been a primary method for exploring interactions between brain regions and decoding brain function. However, traditional FC methods often overlook the intricate, multi-way interplay among brain elements that emerge from the brains densely interconnected nature. To overcome these limitations, we introduce a novel voxel-centric framework that captures the multi-way interactions between voxels and networks identified via high-model order independent component analysis. This framework posits that individual voxels serve as critical mediators of multi-network communication, reflecting the brains complex functional architecture. By encoding voxel contributions from brain networks into binary representations and quantifying the population count at each voxel via Hamming weights, the proposed method prioritizes high-contribution voxels that facilitate inter-network interactions. This approach provides new insights into the brains functional organization, revealing previously unrecognized patterns of voxel-to-network entanglement. Specifically, in the context of schizophrenia, our method enables the identification of spatial patterns that may underpin the cognitive and perceptual disturbances characteristic of the disorder. This enhanced understanding could improve diagnostic precision and help tailor interventions that target specific dysfunctional networks, offering a pathway to more effective treatments and better patient outcomes in schizophrenia.

neuroscience↗

bioRxiv2024

Parallel Multilink Group Joint ICA: Fusion of 3D Structural and 4D Functional Data Across Multiple Resting fMRI Networks

Multimodal neuroimaging research plays a pivotal role in understanding the complexities of the human brain and its disorders. Independent component analysis (ICA) has emerged as a widely used and powerful tool for disentangling mixed independent sources, particularly in the analysis of functional magnetic resonance imaging (fMRI) data. This paper extends the use of ICA as a unifying framework for multimodal fusion, introducing a novel approach termed parallel multilink group joint ICA (pmg-jICA). The method allows for the fusion of gray matter maps from structural MRI (sMRI) data to multiple fMRI intrinsic networks, addressing the limitations of previous models. The effectiveness of pmg-jICA is demonstrated through its application to an Alzheimers dataset, yielding linked structure-function outputs for 53 brain networks. Our approach leverages the complementary information from various imaging modalities, providing a unique perspective on brain alterations in Alzheimers disease. The pmg-jICA identifies several components with significant differences between HC and AD groups including thalamus, caudate, putamen with in the subcortical (SC) domain, insula, parahippocampal gyrus within the cognitive control (CC) domain, and the lingual gyrus within the visual (VS) domain, providing localized insights into the links between AD and specific brain regions. In addition, because we link across multiple brain networks, we can also compute functional network connectivity (FNC) from spatial maps and subject loadings, providing a detailed exploration of the relationships between different brain regions and allowing us to visualize spatial patterns and loading parameters in sMRI along with intrinsic networks and FNC from the fMRI data. In essence, developed approach combines concepts from joint ICA and group ICA to provide a rich set of output characterizing data-driven links between covarying gray matter networks, and a (potentially large number of) resting fMRI networks allowing further study in the context of structure/function links. We demonstrate the utility of the approach by highlighting key structure/function disruptions in Alzheimers individuals.

neuroscience↗

bioRxiv2024

Time-varying Spatial Propagation of Brain Networks in fMRI data

Spontaneous neural activity coherently relays information across the brain. Several efforts have been made to understand how spontaneous neural activity evolves at the macro-scale level as measured by resting-state functional magnetic resonance imaging (rsfMRI). Previous studies observe the global patterns and flow of information in rsfMRI using methods such as sliding window or temporal lags. However, to our knowledge, no studies have examined spatial propagation patterns evolving with time across multiple overlapping 4D networks. Here, we propose a novel approach to study how dynamic states of the brain networks spatially propagate and evaluate whether these propagating states contain information relevant to mental illness. We implement a lagged windowed correlation approach to capture voxel-wise network-specific spatial propagation patterns in dynamic states. Results show systematic spatial state changes over time, which we confirmed are replicable across multiple scan sessions using human connectome project data. We observe networks varying in propagation speed; for example, the default mode network (DMN) propagates slowly and remains positively correlated to blood oxygenation level-dependent (BOLD) signal for 6-8 seconds, whereas the visual network propagates much quicker. We also show that summaries of network specific propagative patterns are linked to schizophrenia. More specifically, we find significant group differences in multiple dynamic parameters between schizophrenia patients and controls within four large-scale networks: default mode, temporal lobe, subcortical, and visual network. Individuals with schizophrenia spend more time in certain propagating states. In summary, this study introduces a promising general approach to exploring the spatial propagation in dynamic states of brain networks and their associated complexity and reveals novel insights into the neurobiology of schizophrenia.

neuroscience↗

bioRxiv2023

Spatial Dynamic Subspaces Encode Sex-Specific Schizophrenia Disruptions in Transient Network Overlap and its Links to Genetic Risk

BackgroundRecent advances in resting-state fMRI allow us to study spatial dynamics, the phenomenon of brain networks spatially evolving over time. However, most dynamic studies still use subject-specific, spatially-static nodes. As recent studies have demonstrated, incorporating time-resolved spatial properties is crucial for precise functional connectivity estimation and gaining unique insights into brain function. Nevertheless, estimating time-resolved networks poses challenges due to the low signal-to-noise ratio, limited information in short time segments, and uncertain identification of corresponding networks within and between subjects. MethodsWe adapt a reference-informed network estimation technique to capture time-resolved spatial networks and their dynamic spatial integration and segregation. We focus on time-resolved spatial functional network connectivity (spFNC), an estimate of network spatial coupling, to study sex-specific alterations in schizophrenia and their links to multi-factorial genomic data. ResultsOur findings are consistent with the dysconnectivity and neurodevelopment hypotheses and align with the cerebello-thalamo-cortical, triple-network, and frontoparietal dysconnectivity models, helping to unify them. The potential unification offers a new understanding of the underlying mechanisms. Notably, the posterior default mode/salience spFNC exhibits sex-specific schizophrenia alteration during the state with the highest global network integration and correlates with genetic risk for schizophrenia. This dysfunction is also reflected in high-dimensional (voxel-level) space in regions with weak functional connectivity to corresponding networks. ConclusionsOur method can effectively capture spatially dynamic networks, detect nuanced SZ effects, and reveal the intricate relationship of dynamic information to genomic data. The results also underscore the potential of dynamic spatial dependence and weak connectivity in the clinical landscape.

neuroscience↗

bioRxiv2020

Modular and state-relevant connectivity in high-frequency resting-state BOLD fMRI data: An independent component analysis

Resting-state fMRI (rs-fMRI) data are typically filtered at different frequency bins between 0.008[~]0.2 Hz (varies across the literature) prior to analysis to mitigate nuisance variables (e.g., drift, motion, cardiac, and respiratory) and maximize the sensitivity to neuronal-mediated BOLD signal. However, multiple lines of evidence suggest meaningful BOLD signal may also be parsed at higher frequencies. To test this notion, a functional network connectivity (FNC) analysis based on a spatially informed independent component analysis (ICA) was performed at seven different bandpass frequency bins to examine FNC matrices across spectra. Further, eyes open (EO) vs. eyes closed (EC) resting-state acquisitions from the same participants were compared across frequency bins to examine if EO vs. EC FNC matrices and randomness estimations of FNC matrices are distinguishable at different frequencies. Results show that FNCs in higher-frequency bins display modular FNC similar to the lowest frequency bin, while r-to-z FNC and FNC-based measures indicating matrix non-randomness were highest in the 0.31-0.46 Hz range relative to all frequency bins above and below this range. As such, the FNC within this range appears to be the most temporally correlated, but the mechanisms facilitating this coherence require further analyses. Compared to EO, EC displayed greater FNC (involved in visual, cognitive control, somatomotor, and auditory domains) and randomness values at lower frequency bins, but this phenomenon flipped (EO > EC) at frequency bins greater than 0.46 Hz, particularly within visual regions. While the effect sizes range from small to large specific to frequency range and resting state (EO vs. EC), with little influence from common artifacts. These differences indicate that unique information can be derived from FNC between BOLD signals at different frequencies relative to a given restingstate acquisition and support the hypothesis meaningful BOLD signal is present at higher frequency ranges.

neuroscience↗