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Description
Autism spectrum disorder (ASD) is a developmental neuropsychiatric condition with early childhood onset, thus most research has focused on characterizing brain function in young individuals. Little is understood about brain function differences in middle age and older adults with ASD, despite evidence of persistent and worsening cognitive symptoms. Functional Magnetic

Autism spectrum disorder (ASD) is a developmental neuropsychiatric condition with early childhood onset, thus most research has focused on characterizing brain function in young individuals. Little is understood about brain function differences in middle age and older adults with ASD, despite evidence of persistent and worsening cognitive symptoms. Functional Magnetic Resonance Imaging (MRI) in younger persons with ASD demonstrate that large-scale brain networks containing the prefrontal cortex are affected. A novel, threshold-selection-free graph theory metric is proposed as a more robust and sensitive method for tracking brain aging in ASD and is compared against five well-accepted graph theoretical analysis methods in older men with ASD and matched neurotypical (NT) participants. Participants were 27 men with ASD (52 +/- 8.4 years) and 21 NT men (49.7 +/- 6.5 years). Resting-state functional MRI (rs-fMRI) scans were collected for six minutes (repetition time=3s) with eyes closed. Data was preprocessed in SPM12, and Data Processing Assistant for Resting-State fMRI (DPARSF) was used to extract 116 regions-of-interest defined by the automated anatomical labeling (AAL) atlas. AAL regions were separated into six large-scale brain networks. This proposed metric is the slope of a monotonically decreasing convergence function (Integrated Persistent Feature, IPF; Slope of the IPF, SIP). Results were analyzed in SPSS using ANCOVA, with IQ as a covariate. A reduced SIP was in older men with ASD, compared to NT men, in the Default Mode Network [F(1,47)=6.48; p=0.02; 2=0.13] and Executive Network [F(1,47)=4.40; p=0.04; 2=0.09], a trend in the Fronto-Parietal Network [F(1,47)=3.36; p=0.07; 2=0.07]. There were no differences in the non-prefrontal networks (Sensory motor network, auditory network, and medial visual network). The only other graph theory metric to reach significance was network diameter in the Default Mode Network [F(1,47)=4.31; p=0.04; 2=0.09]; however, the effect size for the SIP was stronger. Modularity, Betti number, characteristic path length, and eigenvalue centrality were all non-significant. These results provide empirical evidence of decreased functional network integration in pre-frontal networks of older adults with ASD and propose a useful biomarker for tracking prognosis of aging adults with ASD to enable more informed treatment, support, and care methods for this growing population.
ContributorsCatchings, Michael Thomas (Author) / Braden, Brittany B (Thesis advisor) / Greger, Bradley (Thesis advisor) / Schaefer, Sydney (Committee member) / Arizona State University (Publisher)
Created2019
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Description
Measuring node centrality is a critical common denominator behind many important graph mining tasks. While the existing literature offers a wealth of different node centrality measures, it remains a daunting task on how to intervene the node centrality in a desired way. In this thesis, we study the problem of

Measuring node centrality is a critical common denominator behind many important graph mining tasks. While the existing literature offers a wealth of different node centrality measures, it remains a daunting task on how to intervene the node centrality in a desired way. In this thesis, we study the problem of minimizing the centrality of one or more target nodes by edge operation. The heart of the proposed method is an accurate and efficient algorithm to estimate the impact of edge deletion on the spectrum of the underlying network, based on the observation that the edge deletion is essentially a local, sparse perturbation to the original network. Extensive experiments are conducted on a diverse set of real networks to demonstrate the effectiveness, efficiency and scalability of our approach. In particular, it is average of 260.95%, in terms of minimizing eigen-centrality, better than the standard matrix-perturbation based algorithm, with lower time complexity.
ContributorsPeng, Ruiyue (Author) / Tong, Hanghang (Thesis advisor) / He, Jingrui (Committee member) / Davulcu, Hasan (Committee member) / Arizona State University (Publisher)
Created2016
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Description
Higher-rank graphs, or k-graphs, are higher-dimensional analogues of directed graphs, and as with ordinary directed graphs, there are various C*-algebraic objects that can be associated with them. This thesis adopts a functorial approach to study the relationship between k-graphs and their associated C*-algebras. In particular, two functors are given between

Higher-rank graphs, or k-graphs, are higher-dimensional analogues of directed graphs, and as with ordinary directed graphs, there are various C*-algebraic objects that can be associated with them. This thesis adopts a functorial approach to study the relationship between k-graphs and their associated C*-algebras. In particular, two functors are given between appropriate categories of higher-rank graphs and the category of C*-algebras, one for Toeplitz algebras and one for Cuntz-Krieger algebras. Additionally, the Cayley graphs of finitely generated groups are used to define a class of k-graphs, and a functor is then given from a category of finitely generated groups to the category of C*-algebras. Finally, functoriality is investigated for product systems of C*-correspondences associated to k-graphs. Additional results concerning the structural consequences of functoriality, properties of the functors, and combinatorial aspects of k-graphs are also included throughout.
ContributorsEikenberry, Keenan (Author) / Quigg, John (Thesis advisor) / Kaliszewski, Steven (Thesis advisor) / Spielberg, John (Committee member) / Arizona State University (Publisher)
Created2016
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Description
Little is known about how cognitive and brain aging patterns differ in older adults with autism spectrum disorder (ASD). However, recent evidence suggests that individuals with ASD may be at greater risk of pathological aging conditions than their neurotypical (NT) counterparts. A growing body of research indicates that older adults

Little is known about how cognitive and brain aging patterns differ in older adults with autism spectrum disorder (ASD). However, recent evidence suggests that individuals with ASD may be at greater risk of pathological aging conditions than their neurotypical (NT) counterparts. A growing body of research indicates that older adults with ASD may experience accelerated cognitive decline and neurodegeneration as they age, although studies are limited by their cross-sectional design in a population with strong age-cohort effects. Studying aging in ASD and identifying biomarkers to predict atypical aging is important because the population of older individuals with ASD is growing. Understanding the unique challenges faced as autistic adults age is necessary to develop treatments to improve quality of life and preserve independence. In this study, a longitudinal design was used to characterize cognitive and brain aging trajectories in ASD as a function of autistic trait severity. Principal components analysis (PCA) was used to derive a cognitive metric that best explains performance variability on tasks measuring memory ability and executive function. The slope of the integrated persistent feature (SIP) was used to quantify functional connectivity; the SIP is a novel, threshold-free graph theory metric which summarizes the speed of information diffusion in the brain. Longitudinal mixed models were using to predict cognitive and brain aging trajectories (measured via the SIP) as a function of autistic trait severity, sex, and their interaction. The sensitivity of the SIP was also compared with traditional graph theory metrics. It was hypothesized that older adults with ASD would experience accelerated cognitive and brain aging and furthermore, age-related changes in brain network topology would predict age-related changes in cognitive performance. For both cognitive and brain aging, autistic traits and sex interacted to predict trajectories, such that older men with high autistic traits were most at risk for poorer outcomes. In men with autism, variability in SIP scores across time points trended toward predicting cognitive aging trajectories. Findings also suggested that autistic traits are more sensitive to differences in brain aging than diagnostic group and that the SIP is more sensitive to brain aging trajectories than other graph theory metrics. However, further research is required to determine how physiological biomarkers such as the SIP are associated with cognitive outcomes.
ContributorsSullivan, Georgia (Author) / Braden, Blair (Thesis advisor) / Kodibagkar, Vikram (Thesis advisor) / Schaefer, Sydney (Committee member) / Wang, Yalin (Committee member) / Arizona State University (Publisher)
Created2022