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Showing papers by "Allan L. Reiss published in 2018"


Journal ArticleDOI
TL;DR: Topological Data Analysis is used to reveal the overall organization of whole-brain activity maps at a single-participant level—as an interactive representation—without arbitrarily collapsing data in space or time.
Abstract: Little is known about how our brains dynamically adapt for efficient functioning. Most previous work has focused on analyzing changes in co-fluctuations between a set of brain regions over several temporal segments of the data. We argue that by collapsing data in space or time, we stand to lose useful information about the brain’s dynamical organization. Here we use Topological Data Analysis to reveal the overall organization of whole-brain activity maps at a single-participant level—as an interactive representation—without arbitrarily collapsing data in space or time. Using existing multitask fMRI datasets, with the known ground truth about the timing of transitions from one task-block to next, our approach tracks both within- and between-task transitions at a much faster time scale (~4–9 s) than before. The individual differences in the revealed dynamical organization predict task performance. In summary, our approach distills complex brain dynamics into interactive and behaviorally relevant representations. Approaches describing how the brain changes to accomplish cognitive tasks tend to rely on collapsed data. Here, authors present a new approach that maintains high dimensionality and use it to describe individual differences in how brain activity is represented and organized across different cognitive tasks.

187 citations


Journal ArticleDOI
24 Aug 2018-PLOS ONE
TL;DR: Results from the first fNIRS-based investigation of fronto-parietal signatures of cortical activation and functional connectivity during a computer-based visuospatial working memory task indicate that the local maxima of corticalactivation and functional coherence do not necessarily overlap spatially and that cortical activation is significantly more susceptible to task-specific demands compared to functional connectivity.
Abstract: Demands on visuospatial working memory are a ubiquitous part of everyday life. As such, significant efforts have been made to understand how the brain responds to these demands in real-world environments. Multiple brain imaging studies have highlighted a fronto-parietal cortical network that underlies visuospatial working memory, is modulated by cognitive load, and that appears to respond uniquely to encoding versus retrieval components. Furthermore, multiple studies have identified functional connectivity in regions of the fronto-parietal network during working memory tasks. Together, these findings have helped outline important aspects of the neural architecture that underlies visuospatial working memory. Here, we provide results from the first fNIRS-based investigation of fronto-parietal signatures of cortical activation and functional connectivity during a computer-based visuospatial working memory task. Our results indicate that the local maxima of cortical activation and functional coherence do not necessarily overlap spatially, and that cortical activation is significantly more susceptible to task-specific demands compared to functional connectivity. These results highlight important and novel information regarding neurotypical signatures of cortical activation and functional connectivity during visuospatial working memory. Our findings also demonstrate the utility of fNIRS for interrogating these cognitive processes.

39 citations


Journal ArticleDOI
TL;DR: It is suggested that hyperglycaemia is associated with altered white matter development, which may contribute to the mild cognitive deficits in this population of children with type 1 diabetes.
Abstract: Prior studies suggest white matter growth is reduced and white matter microstructure is altered in the brains of young children with type 1 diabetes when compared with brains of non-diabetic children, due in part to adverse effects of hyperglycaemia. This longitudinal observational study examines whether dysglycaemia alters the developmental trajectory of white matter microstructure over time in young children with type 1 diabetes. One hundred and eighteen children, aged 4 to <10 years old with type 1 diabetes and 58 age-matched, non-diabetic children were studied at baseline and 18 months, at five Diabetes Research in Children Network clinical centres. We analysed longitudinal trajectories of white matter using diffusion tensor imaging. Continuous glucose monitoring profiles and HbA1c levels were obtained every 3 months. Axial diffusivity was lower in children with diabetes at baseline (p = 0.022) and at 18 months (p = 0.015), indicating that differences in white matter microstructure persist over time in children with diabetes. Within the diabetes group, lower exposure to hyperglycaemia, averaged over the time since diagnosis, was associated with higher fractional anisotropy (p = 0.037). Fractional anisotropy was positively correlated with performance (p < 0.002) and full-scale IQ (p < 0.02). These results suggest that hyperglycaemia is associated with altered white matter development, which may contribute to the mild cognitive deficits in this population.

31 citations


Journal ArticleDOI
TL;DR: Twins with ASD had thalamic abnormalities relative to controls/unaffected co‐twins, and neurometabolite levels were correlated with multiple symptom domains.
Abstract: Multiple lines of research have reported thalamic abnormalities in individuals with autism spectrum disorder (ASD) that are associated with social communication impairments (SCI), restricted and repetitive behaviors (RRB), or sensory processing abnormalities (SPA). Thus, the thalamus may represent a common neurobiological structure that is shared across symptom domains in ASD. Same-sex monozygotic (MZ) and dizygotic (DZ) twin pairs with and without ASD underwent cognitive/behavioral evaluation and magnetic resonance imaging to assess the thalamus. Neurometabolites were measured with 1H magnetic resonance spectroscopy (MRS) utilizing a multi-voxel PRESS sequence and were referenced to creatine+phosphocreatine (tCr). N-acetyl aspartate (NAA), a marker of neuronal integrity, was reduced in twins with ASD (n=47) compared to typically-developing (TD) controls (n=33), and this finding was confirmed in a sub-sample of co-twins discordant for ASD (n=11). NAA in the thalamus was correlated to a similar extent with SCI, RRB, and SPA, such that reduced neuronal integrity was associated with greater symptom severity. Glutamate+glutamine (Glx) was also reduced in affected versus unaffected co-twins. Additionally, NAA and Glx appeared to be primarily genetically-mediated, based on comparisons between MZ and DZ twin pairs. Thus, thalamic abnormalities may be influenced by genetic susceptibility for ASD but are likely not domain-specific.

26 citations


Journal ArticleDOI
TL;DR: Relationships among cortical activation, steering control, and individual personality traits suggest that individual brain states and traits may be useful in predicting a driver's response to changes in vehicle dynamics.
Abstract: Improvements in vehicle safety require understanding of the neural systems that support the complex, dynamic task of real-world driving. We used functional near infrared spectroscopy (fNIRS) and pupilometry to quantify cortical and physiological responses during a realistic, simulated driving task in which vehicle dynamics were manipulated. Our results elucidate compensatory changes in driver behavior in response to changes in vehicle handling. We also describe associated neural and physiological responses under different levels of mental workload. The increased cortical activation we observed during the late phase of the experiment may indicate motor learning in prefrontal-parietal networks. Finally, relationships among cortical activation, steering control, and individual personality traits suggest that individual brain states and traits may be useful in predicting a driver's response to changes in vehicle dynamics. Results such as these will be useful for informing the design of automated safety systems that facilitate safe and supportive driver-car communication.

25 citations


Journal ArticleDOI
TL;DR: Although longitudinal hippocampus growth did not differ between children with T1D and healthy control children, slower growth of the hippocampus was associated with both increased exposure to hyperglycemia (interval HbA1c) and greater glycemic variability (MAGE) in T1C.
Abstract: The extant literature finds that children with type 1 diabetes mellitus (T1D) experience mild cognitive alterations compared to healthy age-matched controls. The neural basis of these cognitive differences is unclear but may relate in part to the effects of dysglycemia on the developing brain. We investigated longitudinal changes in hippocampus volume in young children with early-onset T1D. Structural magnetic resonance imaging data were acquired from 142 children with T1D and 65 age-matched control subjects (4-10 years of age at study entry) at 2 time points, 18 months apart. The effects of diabetes and glycemic exposure on hippocampal volume and growth were examined. Results indicated that although longitudinal hippocampus growth did not differ between children with T1D and healthy control children, slower growth of the hippocampus was associated with both increased exposure to hyperglycemia (interval HbA1c) and greater glycemic variability (MAGE) in T1D. These observations indicate that the current practice of tolerating some hyperglycemia to minimize the risk of hypoglycemia in young children with T1D may not be optimal for the developing brain. Efforts that continue to assess the factors influencing neural and cognitive development in children with T1D will be critical in minimizing the deleterious effects of diabetes.

22 citations


Journal ArticleDOI
TL;DR: The findings indicate that X-monosomy contributes affects to attention networks and cognitive dysfunction that might increase risk for ADHD, which has clinical relevance for girls with TS and might also serve as a biological marker in future research examining the effects of the intervention that targets attention skills.
Abstract: Attention deficit hyperactivity disorder (ADHD) is strongly affected by sex, but sex chromosomes' effect on brain attention networks and cognition are difficult to examine in humans. This is due to significant etiologic heterogeneity among diagnosed individuals. In contrast, individuals with Turner syndrome (TS), who have substantially increased risk for ADHD symptoms, share a common genetic risk factor related to the absence of the X-chromosome, thus serving as a more homogeneous genetic model. Resting-state functional MRI was employed to examine differences in attention networks between girls with TS (n = 40) and age- sex- and Tanner-matched controls (n = 33). We compared groups on resting-state functional connectivity measures from data-driven independent components analysis (ICA) and hypothesis-based seed analysis. Using ICA, reduced connectivity was observed in both frontoparietal and dorsal attention networks. Similarly, using seeds in the bilateral intraparietal sulcus (IPS), reduced connectivity was observed between IPS and frontal and cerebellar regions. Finally, we observed a brain-behavior correlation between IPS-cerebellar connectivity and cognitive attention measures. These findings indicate that X-monosomy contributes affects to attention networks and cognitive dysfunction that might increase risk for ADHD. Our findings not only have clinical relevance for girls with TS, but might also serve as a biological marker in future research examining the effects of the intervention that targets attention skills.

17 citations


Journal ArticleDOI
TL;DR: Adolescents and young adults with FXS demonstrate neuroanatomical abnormalities consistent with those previously reported in children and adults with fragile X syndrome, likely result from reduced FMRP during early neurodevelopment and mediate downstream deleterious effects on cognitive function.

12 citations


Book ChapterDOI
01 Jan 2018
TL;DR: Hawthorne et al. as mentioned in this paper used a distilled version of Creative Gym, a course that has been taught at the d.school for the past 8 years that is purely focused on individual creativity skill building in a group environment.
Abstract: Creativity is an important construct driving society and innovation forward. Many organizations have adopted team-based work in order to increase innovation and creativity under the assumption that groups of people tend to produce more creative ideas than individuals. Research has so far shown mixed results with some finding enhanced creativity in teams while others showing the opposite effect. A short literature review of team creativity and how it relates to possible neural networks is presented. In addition, we will integrate key findings from our current research implementing a group training protocol to enhance creative capacity. Participants in our creativity study underwent a distilled version of Creative Gym, a course that has been taught at the d.school for the past 8 years that is purely focused on individual creativity skill building in a group environment. Students enhance their creative confidence and sharpen their individual design thinking skills through hands-on experiences that are comprised of unconventional hands-on exercises organized around nine core themes that engage our human abilities in intersecting ways. Training was performed in a group environment while improving perspective taking, empathy, synthesizing ideas and developing improvisational skills. Creativity was measured, before and after participant training (Time 1 and Time 2), using standardized assessments of creativity. In addition to neuroimaging markers, other cognitive faculties (e.g. executive functioning) and personality were also assessed before and after training (Hawthorne, et al. Design thinking research. Springer, 2014). We will review the literature on team creativity and present key findings from our current research, using group based creativity skill training.

5 citations


Journal ArticleDOI
TL;DR: This case was recorded during the Diabetes Research in Children Network (DirecNet) longitudinal study, in which children had MRI scans at three time points over 5 years, and one subject with diabetes had unusually large brain volume changes from age 6.5 to age 8.0 years.
Abstract: This case was recorded during the Diabetes Research in Children Network (DirecNet) longitudinal study (1), in which children ( N = 214) had MRI scans at three time points over 5 years. During the analyses, we noted that one subject with diabetes had unusually large brain volume changes (13.5% decrease of gray matter volume and 165% increase in ventricular volume) from age 6.5 to age 8.0 years. The patient was diagnosed with type 1 diabetes at age 5.6 years when he presented without diabetic ketoacidosis. Neuroradiological reviews of the MRI scans at each time point reported no evidence of gross pathological abnormalities or diffusion restrictions. The patient was on multiple daily insulin injections at the time of his first MRI scan and on infusion pump therapy at the later scans. He was healthy besides type 1 diabetes, prepubertal, with full-term birth, normal weight development, normal thyroid function, and no evidence of neurological deficits. Moreover, he had age-appropriate vocabulary and stable cognitive test scores over the 5-year period. His medical …

1 citations


Journal ArticleDOI
TL;DR: A new two-sample testing procedure is proposed that compares associations between two tables in two groups and is consistent with the hypothesis that girls with TS have a different brain-cognition association structure than healthy controls.
Abstract: Girls and women with Turner syndrome (TS) have a completely or partially missing X chromosome. Extensive studies on the impact of TS on neuroanatomy and cognition have been conducted. The integration of neuroanatomical and cognitive information into one consistent analysis through multi-table methods is difficult and most standard tests are underpowered. We propose a new two-sample testing procedure that compares associations between two tables in two groups. The procedure combines multi-table methods with permutation tests. In particular, we construct cluster size test statistics that incorporate spatial dependencies. We apply our new procedure to a newly collected dataset comprising of structural brain scans and cognitive test scores from girls with TS and healthy control participants (age and sex matched). We measure neuroanatomy with Tensor-Based Morphometry (TBM) and cognitive function with Wechsler IQ and NEuroPSYchological tests (NEPSY-II). We compare our multi-table testing procedure to a single-table analysis. Our new procedure reports differential correlations between two voxel clusters and a wide range of cognitive tests whereas the single-table analysis reports no differences. Our findings are consistent with the hypothesis that girls with TS have a different brain-cognition association structure than healthy controls.