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Alex D. Leow

Publications and source records attributed to Alex D. Leow.

9 recordsLinked to original sources

Longitudinal Bayesian Learning of Continuous Disease Position across the Alzheimer's Disease Continuum

Alzheimer's disease (AD) progresses as a continuous biological process, whereas most existing neuroimaging-based artificial intelligence methods remain limited to discrete diagnosis or clinical score prediction from cross-sectional imaging. In this work, we propose Disease Continuum Positioning (DCP), a longitudinal Bayesian Learning framework that continuously estimates disease severity from longitudinal diffusion tensor imaging (DTI). Specifically, DCP models disease severity as a low-dimensional probabilistic latent variable by jointly integrating longitudinal observations with weak clinical supervision, from which the proposed Disease Continuum Score (DCS) is derived to quantify an individual's position along the Alzheimer's disease continuum together with its associated uncertainty. Extensive experiments on the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort demonstrate that DCP consistently outperforms representative disease progression methods. More importantly, comprehensive validation analyses show that DCS accurately characterizes disease severity, exhibits strong clinical relevance, preserves longitudinal disease evolution, and predicts future disease conversion. These results suggest that DCS provides a quantitative imaging-derived representation for continuous assessment of Alzheimer's disease progression beyond conventional diagnostic labels and clinical scores.

cs.LG

EEG Classification based on Image Configuration in Social Anxiety Disorder

The problem of detecting the presence of Social Anxiety Disorder (SAD) using Electroencephalography (EEG) for classification has seen limited study and is addressed with a new approach that seeks to exploit the knowledge of EEG sensor spatial configuration. Two classification models, one which ignores the configuration (model 1) and one that exploits it with different interpolation methods (model 2), are studied. Performance of these two models is examined for analyzing 34 EEG data channels each consisting of five frequency bands and further decomposed with a filter bank. The data are collected from 64 subjects consisting of healthy controls and patients with SAD. Validity of our hypothesis that model 2 will significantly outperform model 1 is borne out in the results, with accuracy $6$--$7\%$ higher for model 2 for each machine learning algorithm we investigated. Convolutional Neural Networks (CNN) were found to provide much better performance than SVM and kNNs.

cs.LG

dpMood: Exploiting Local and Periodic Typing Dynamics for Personalized Mood Prediction

Mood disorders are common and associated with significant morbidity and mortality. Early diagnosis has the potential to greatly alleviate the burden of mental illness and the ever increasing costs to families and society. Mobile devices provide us a promising opportunity to detect the users' mood in an unobtrusive manner. In this study, we use a custom keyboard which collects keystrokes' meta-data and accelerometer values. Based on the collected time series data in multiple modalities, we propose a deep personalized mood prediction approach, called {\pro}, by integrating convolutional and recurrent deep architectures as well as exploring each individual's circadian rhythm. Experimental results not only demonstrate the feasibility and effectiveness of using smart-phone meta-data to predict the presence and severity of mood disturbances in bipolar subjects, but also show the potential of personalized medical treatment for mood disorders.

cs.HC

Exact Combinatorial Inference for Brain Images

The permutation test is known as the exact test procedure in statistics. However, often it is not exact in practice and only an approximate method since only a small fraction of every possible permutation is generated. Even for a small sample size, it often requires to generate tens of thousands permutations, which can be a serious computational bottleneck. In this paper, we propose a novel combinatorial inference procedure that enumerates all possible permutations combinatorially without any resampling. The proposed method is validated against the standard permutation test in simulation studies with the ground truth. The method is further applied in twin DTI study in determining the genetic contribution of the minimum spanning tree of the structural brain connectivity.

stat.CO

Multi-View Multi-Graph Embedding for Brain Network Clustering Analysis

Network analysis of human brain connectivity is critically important for understanding brain function and disease states. Embedding a brain network as a whole graph instance into a meaningful low-dimensional representation can be used to investigate disease mechanisms and inform therapeutic interventions. Moreover, by exploiting information from multiple neuroimaging modalities or views, we are able to obtain an embedding that is more useful than the embedding learned from an individual view. Therefore, multi-view multi-graph embedding becomes a crucial task. Currently, only a few studies have been devoted to this topic, and most of them focus on the vector-based strategy which will cause structural information contained in the original graphs lost. As a novel attempt to tackle this problem, we propose Multi-view Multi-graph Embedding (M2E) by stacking multi-graphs into multiple partially-symmetric tensors and using tensor techniques to simultaneously leverage the dependencies and correlations among multi-view and multi-graph brain networks. Extensive experiments on real HIV and bipolar disorder brain network datasets demonstrate the superior performance of M2E on clustering brain networks by leveraging the multi-view multi-graph interactions.

cs.LG

DeepMood: Modeling Mobile Phone Typing Dynamics for Mood Detection

The increasing use of electronic forms of communication presents new opportunities in the study of mental health, including the ability to investigate the manifestations of psychiatric diseases unobtrusively and in the setting of patients' daily lives. A pilot study to explore the possible connections between bipolar affective disorder and mobile phone usage was conducted. In this study, participants were provided a mobile phone to use as their primary phone. This phone was loaded with a custom keyboard that collected metadata consisting of keypress entry time and accelerometer movement. Individual character data with the exceptions of the backspace key and space bar were not collected due to privacy concerns. We propose an end-to-end deep architecture based on late fusion, named DeepMood, to model the multi-view metadata for the prediction of mood scores. Experimental results show that 90.31% prediction accuracy on the depression score can be achieved based on session-level mobile phone typing dynamics which is typically less than one minute. It demonstrates the feasibility of using mobile phone metadata to infer mood disturbance and severity.

cs.HC

Sex-by-age differences in the resting-state brain connectivity

Recently we developed a novel method for assessing the hierarchical modularity of functional brain networks - the probability associated community estimation(PACE). The PACE algorithm is unique in that it permits a dual formulation, thus yielding equivalent connectome modular structure regardless of whether considering positive or negative edges. This method was rigorously validated using F1000 and HCP data. We detected novel sex differences in resting-state connectivity that were not previously reported. This current study more thoroughly examined sex differences as a function of age and their clinical correlates, with findings supporting a basal configuration framework. To this end, we found that men and women do not significantly differ in the 22-25 age range. However, these same non-significant differences attained statistical significance in the 26-30 age group, while becoming highly statistically significant in the 31-35 age group. At the most global level, areas of diverging sex difference include parts of the prefrontal cortex and the temporal lobe, amygdala, hippocampus, inferior parietal lobule, posterior cingulate, and precuneus. Further, we identified statistically different self-reported summary scores of inattention, hyperactivity, and anxiety problems between men and women. These self-reports additionally divergently interact with age and the basal configuration between sexes. In sum, our study supports a paradigm change in how we conceptualize the functional connectome, shifting away from simple concepts, and towards thinking globally and probabilistically how the brain exhibits dynamic sex-specific connectivity configuration as a function of age, and the role this sex-by-age configuration at rest might play in mental health frequency and presentation, including symptom patterns in depression.

q-bio.NC

Exploring the Human Connectome Topology in Group Studies

Visually comparing brain networks, or connectomes, is an essential task in the field of neuroscience. Especially relevant to the field of clinical neuroscience, group studies that examine differences between populations or changes over time within a population enable neuroscientists to reason about effective diagnoses and treatments for a range of neuropsychiatric disorders. In this paper, we specifically explore how visual analytics tools can be used to facilitate various clinical neuroscience tasks, in which observation and analysis of meaningful patterns in the connectome can support patient diagnosis and treatment. We conduct a survey of visualization tasks that enable clinical neuroscience activities, and further explore how existing connectome visualization tools support or fail to support these tasks. Based on our investigation of these tasks, we introduce a novel visualization tool, NeuroCave, to support group studies analyses. We discuss how our design decisions (the use of immersive visualization, the use of hierarchical clustering and dimensionality reduction techniques, and the choice of visual encodings) are motivated by these tasks. We evaluate NeuroCave through two use cases that illustrate the utility of interactive connectome visualization in clinical neuroscience contexts. In the first use case, we study sex differences using functional connectomes and discover hidden connectome patterns associated with well-known cognitive differences in spatial and verbal abilities. In the second use case, we show how the utility of visualizing the brain in different topological space coupled with clustering information can reveal the brain's intrinsic structure.

q-bio.NC

The Importance of Being Negative: A serious treatment of non-trivial edges in brain functional connectome

Understanding the modularity of fMRI-derived brain networks or connectomes can inform the study of brain function organization. However, fMRI connectomes additionally involve negative edges, which are not rigorously accounted for by existing approaches to modularity that either ignores or arbitrarily weight these connections. Furthermore, most Q maximization-based modularity algorithms yield variable results with suboptimal reproducibility. Here we present an alternative, reproducible approach that exploits how frequent the BOLD-signal correlation between two nodes is negative. We validated this novel probability-based modularity approach on two independent publicly-available resting-state connectome dataset (the Human Connectome Project and the 1000 Functional Connectomes) and demonstrated that negative correlations alone are sufficient in understanding resting-state modularity. In fact, this approach a) permits a dual formulation, leading to equivalent solutions regardless of whether one considers positive or negative edges; b) is theoretically linked to the Ising model defined on the connectome, thus yielding modularity result that maximizes data likelihood. We additionally were able to detect sex differences in modularity that the most widely utilized methods did not. Results confirmed the superiority of our approach in that: a) correlations with the highest probability of being negative are consistently placed between modules, b) due to the equivalent dual forms, no arbitrary weighting factor is required to balance the influence between negative and positive correlations, unlike existing Q maximization-based modularity approaches. As datasets like HCP become widely available for analysis by the neuroscience community at large, appropriate computational tools to understand the neurobiological information of negative edges in fMRI connectomes are increasingly important.

q-bio.QM