1,343 research outputs found
Non-parametric resampling of random walks for spectral network clustering
Parametric resampling schemes have been recently introduced in complex
network analysis with the aim of assessing the statistical significance of
graph clustering and the robustness of community partitions. We propose here a
method to replicate structural features of complex networks based on the
non-parametric resampling of the transition matrix associated with an unbiased
random walk on the graph. We test this bootstrapping technique on synthetic and
real-world modular networks and we show that the ensemble of replicates
obtained through resampling can be used to improve the performance of standard
spectral algorithms for community detection.Comment: 5 pages, 2 figure
Development Of Human Brain Network Architecture Underlying Executive Function
The transition from late childhood to adulthood is characterized by refinements in brain structure and function that support the dynamic control of attention and goal-directed behavior. One broad domain of cognition that undergoes particularly protracted development is executive function, which encompasses diverse cognitive processes including working memory, inhibitory control, and task switching. Delineating how white matter architecture develops to support specialized brain circuits underlying individual differences in executive function is critical for understanding sources of risk-taking behavior and mortality during adolescence. Moreover, neuropsychiatric disorders are increasingly understood as disorders of brain development, are marked by failures of executive function, and are linked to the disruption of evolving brain connectivity.
Network theory provides a parsimonious framework for modeling how anatomical white matter pathways support synchronized fluctuations in neural activity. However, only sparse data exists regarding how the maturation of white matter architecture during human brain development supports coordinated fluctuations in neural activity underlying higher-order cognitive ability. To address this gap, we capitalize on multi-modal neuroimaging and cognitive phenotyping data collected as part of the Philadelphia Neurodevelopmental Cohort (PNC), a large community-based study of brain development.
First, diffusion tractography methods were applied to characterize how the development of structural brain network topology supports domain-specific improvements in cognitive ability (n=882, ages 8-22 years old). Second, structural connectivity and task-based functional connectivity approaches were integrated to describe how the development of anatomical constraints on functional communication support individual differences in executive function (n=727, ages 8-23 years old). Finally, the systematic impact of head motion artifact on measures of structural connectivity were characterized (n=949, ages 8-22 years old), providing important guidelines for studying the development of structural brain network architecture.
Together, this body of work expands our understanding of how developing white matter connectivity in youth supports the emergence of functionally specialized circuits underlying executive processing. As diverse types of psychopathology are increasingly linked to atypical brain maturation, these findings could collectively lead to earlier diagnosis and personalized interventions for individuals at risk for developing mental disorders
Mapping change in large networks
Change is a fundamental ingredient of interaction patterns in biology,
technology, the economy, and science itself: Interactions within and between
organisms change; transportation patterns by air, land, and sea all change; the
global financial flow changes; and the frontiers of scientific research change.
Networks and clustering methods have become important tools to comprehend
instances of these large-scale structures, but without methods to distinguish
between real trends and noisy data, these approaches are not useful for
studying how networks change. Only if we can assign significance to the
partitioning of single networks can we distinguish meaningful structural
changes from random fluctuations. Here we show that bootstrap resampling
accompanied by significance clustering provides a solution to this problem. To
connect changing structures with the changing function of networks, we
highlight and summarize the significant structural changes with alluvial
diagrams and realize de Solla Price's vision of mapping change in science:
studying the citation pattern between about 7000 scientific journals over the
past decade, we find that neuroscience has transformed from an
interdisciplinary specialty to a mature and stand-alone discipline.Comment: 10 pages, 4 figure
Phase transitions of Integrated Information in the Generalized Ising Model of the Brain
The bold framework of the Integrated Information Theory of consciousness are explored in this thesis in the context of the generalized Ising model of the brain. Small 5-node networks are simulated on the Ising model with Metropolis transitions where the fitting parameter T is fit to empirical functional connectivity matrices of healthy human subjects. Fitting to criticality, results indicate that integrated information undergoes a phase transition at the critical temperature Tc. The results are interpreted in the context of an emerging perspective of the science of complexity and perhaps even the philosophy of science; the universe as a self-organizing critical system undergoing cascades of phase transitions into complexity
Age-Related Changes in Human Anatomical and Functional Brain Networks
Thesis (Ph.D.) - Indiana University, Psychological and Brain Sciences, 2015i) The first component characterizes age-related changes in specific connections. We find that functional connections within and between intrinsic connectivity networks (ICNs) follow distinct lifespan trajectories. We further characterize these changes in terms of each ICN’s “modularity” and find that most ICNs become less modular (i.e. less segregated) with age. In anatomical networks we find that hub regions are disproportionately affected by age and become less efficiently connected to the rest of the brain. Finally, we find that, with age stronger functional connections are supported by longer (multi-step) anatomical pathways for communication. ii) The second component is concerned with characterizing age-related changes in the boundaries of ICNs. To this end we used a multi-layer variant of modularity maximization to decompose networks into modules at different organizational scales, which we find exhibit scale-specific trends with age. At coarse scales, for example, we find that modules become more segregated whereas modules defined at finer scales become less segregated. We also find that module composition changes with age, and specific areas associated with memory change their module allegiance with age. iii) In the final component we use generative models to uncover wiring rules for the anatomical brain networks. Modeling network growth as a spatial penalty combined with homophily, we find that we can generate synthetic networks with many of the same properties as real-world brain networks. Fitting this model to individuals, we show that the parameter governing the severity of the spatial penalty weakens monotonically with age and that the overall ability to reproduce realistic connectomes for older individuals suffers. These results suggest that, with age, additional constraints may play an important role in shaping the topology of brain structural networks
Quantitative diffusion MRI with application to multiple sclerosis
Diffusion MRI (dMRI) is a uniquely non-invasive probe of biological tissue properties, increasingly able to provide access to ever more intricate structural and microstructural tissue information. Imaging biomarkers that reveal pathological alterations can help advance our knowledge of complex neurological disorders such as multiple sclerosis (MS), but depend on both high quality image data and robust post-processing pipelines. The overarching aim of this thesis was to develop methods to improve the characterisation of brain tissue structure and microstructure using dMRI. Two distinct avenues were explored. In the first approach, network science and graph theory were used to identify core human brain networks with improved sensitivity to subtle pathological damage. A novel consensus subnetwork was derived using graph partitioning techniques to select nodes based on independent measures of centrality, and was better able to explain cognitive impairment in relapsing-remitting MS patients than either full brain or default mode networks. The influence of edge weighting scheme on graph characteristics was explored in a separate study, which contributes to the connectomics field by demonstrating how study outcomes can be affected by an aspect of network design often overlooked. The second avenue investigated the influence of image artefacts and noise on the accuracy and precision of microstructural tissue parameters. Correction methods for the echo planar imaging (EPI) Nyquist ghost artefact were systematically evaluated for the first time in high b-value dMRI, and the outcomes were used to develop a new 2D phase-corrected reconstruction framework with simultaneous channel-wise noise reduction appropriate for dMRI. The technique was demonstrated to alleviate biases associated with Nyquist ghosting and image noise in dMRI biomarkers, but has broader applications in other imaging protocols that utilise the EPI readout. I truly hope the research in this thesis will influence and inspire future work in the wider MR community
Flexible Coordinator and Switcher Hubs for Adaptive Task Control
Functional connectivity (FC) studies have identified at least two large-scale neural systems that constitute cognitive control networks, the frontoparietal network (FPN) and cingulo-opercular network (CON). Control networks are thought to support goal-directed cognition and behavior. It was previously shown that the FPN flexibly shifts its global connectivity pattern according to task goal, consistent with a “flexible hub” mechanism for cognitive control. Our aim was to build on this finding to develop a functional cartography (a multimetric profile) of control networks in terms of dynamic network properties. We quantified network properties in (male and female) humans using a high-control-demand cognitive paradigm involving switching among 64 task sets. We hypothesized that cognitive control is enacted by the FPN and CON via distinct but complementary roles reflected in network dynamics. Consistent with a flexible “coordinator” mechanism, FPN connections were varied across tasks, while maintaining within-network connectivity to aid cross-region coordination. Consistent with a flexible “switcher” mechanism, CON regions switched to other networks in a task-dependent manner, driven primarily by reduced within-network connections to other CON regions. This pattern of results suggests FPN acts as a dynamic, global coordinator of goal-relevant information, while CON transiently disbands to lend processing resources to other goal-relevant networks. This cartography of network dynamics reveals a dissociation between two prominent cognitive control networks, suggesting complementary mechanisms underlying goal-directed cognition
The topology of structural brain connectivity in diseases and spatio-temporal connectomics
The brain is a complex system, composed of multiple neural units interconnected at different spatial and temporal scales. Diffusion MRI allows probing in vivo the anatomical connectivity between different cortical areas through white matter tracts. In parallel, functional MRI records neural-related signals of brain activity. Particularly, during rest (in absence of specific external task) reproducible dynamical patterns of functional synchronization have been shown across different brain areas. This rich information can be conveniently represented in the form of a graph, a mathematical object where nodes correspond to cortical regions and are connected by edges representing anatomical connections. On the top of this structural network, or brain connectome, individual nodes are associated to functional signals representing neural activity over observation periods. Network science has fundamentally contributed to the characterization of the human connectome. The brain is a small-world network, able to combine segregation and integration aspects. These properties allow functional specialization on the one side, and efficient communication between distant brain areas on the other side, supporting complex cognitive and executive functions. Graph theoretical methods quantify brain topological properties, and allow their comparison between different populations and conditions. In fact, brain connectivity patterns and interdependences between anatomical substrate and functional synchronization have been proved to be impaired in a variety of brain disorders, and to change across human development and aging. Despite these important advancements in the understanding of the brain structure and functioning, many questions are currently unanswered. It is not clear for instance how structural connectivity features are related to individual cognitive capabilities and deficits, and if they have the concrete potential to distinguish pathological subgroups for early diagnosis of brain diseases. Most importantly, it is not yet understood how the connectome topology relates to specific brain functions, and how the transmission of information happens on the top of the structural connectivity infrastructure in order to generate observed functional dynamics. This thesis was motivated by these interdisciplinary inputs, and is the result of a strong interaction between biological and clinical questions on the one hand, and methodological development needs on the other hand. First, we have contributed to the characterization of the human connectome in health and pathologies by adapting and developing network measures for the description of the brain architecture at different scales. Particularly, we have focused on the topological characterization of subnetworks role within the overall brain network. Importantly, we have shown that the topological alteration of distinct brain subsystems may be a biomarker for different brain disorders. Second, we have proposed an original network model for the joint representation of brain structural and functional connectivity properties. This flexible spatio-temporal framework allows the investigation of functional dynamics at multiple temporal scales. Importantly, the investigation of spatio-temporal graphs in healthy subjects have allowed to disclose temporal relationships between local brain activations in resting state recordings, and has highlighted functional communication principles across the brain structural network
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