4,939 research outputs found
Neural mechanisms of resistance to peer influence in early adolescence
During the shift from a parent-dependent child to a fully autonomous adult, peers take on a significant role in shaping the adolescent’s behaviour. Peer-derived influences are not always positive, however. Here we explore neural correlates of inter-individual differences in the probability of resisting peer influence in early adolescence. Using functional magnetic-resonance imaging (fMRI), we found striking differences between 10-year old children with high and low resistance to peer influence in their brain activity during observation of angry hand-movements and angry facial expressions: compared with subjects with low resistance to peer influence, individuals with high resistance showed a highly coordinated brain activity in neural systems underlying perception of action and decision making. These findings suggest that the probability of resisting peer influence depends on neural interactions during observation of emotion-laden actions
At risk of being risky: The relationship between "brain age" under emotional states and risk preference.
Developmental differences regarding decision making are often reported in the absence of emotional stimuli and without context, failing to explain why some individuals are more likely to have a greater inclination toward risk. The current study (N=212; 10-25y) examined the influence of emotional context on underlying functional brain connectivity over development and its impact on risk preference. Using functional imaging data in a neutral brain-state we first identify the "brain age" of a given individual then validate it with an independent measure of cortical thickness. We then show, on average, that "brain age" across the group during the teen years has the propensity to look younger in emotional contexts. Further, we show this phenotype (i.e. a younger brain age in emotional contexts) relates to a group mean difference in risk perception - a pattern exemplified greatest in young-adults (ages 18-21). The results are suggestive of a specified functional brain phenotype that relates to being at "risk to be risky.
Multiple Holdouts With Stability: Improving the Generalizability of Machine Learning Analyses of Brain-Behavior Relationships.
BACKGROUND:In 2009, the National Institute of Mental Health launched the Research Domain Criteria, an attempt to move beyond diagnostic categories and ground psychiatry within neurobiological constructs that combine different levels of measures (e.g., brain imaging and behavior). Statistical methods that can integrate such multimodal data, however, are often vulnerable to overfitting, poor generalization, and difficulties in interpreting the results. METHODS:We propose an innovative machine learning framework combining multiple holdouts and a stability criterion with regularized multivariate techniques, such as sparse partial least squares and kernel canonical correlation analysis, for identifying hidden dimensions of cross-modality relationships. To illustrate the approach, we investigated structural brain-behavior associations in an extensively phenotyped developmental sample of 345 participants (312 healthy and 33 with clinical depression). The brain data consisted of whole-brain voxel-based gray matter volumes, and the behavioral data included item-level self-report questionnaires and IQ and demographic measures. RESULTS:Both sparse partial least squares and kernel canonical correlation analysis captured two hidden dimensions of brain-behavior relationships: one related to age and drinking and the other one related to depression. The applied machine learning framework indicates that these results are stable and generalize well to new data. Indeed, the identified brain-behavior associations are in agreement with previous findings in the literature concerning age, alcohol use, and depression-related changes in brain volume. CONCLUSIONS:Multivariate techniques (such as sparse partial least squares and kernel canonical correlation analysis) embedded in our novel framework are promising tools to link behavior and/or symptoms to neurobiology and thus have great potential to contribute to a biologically grounded definition of psychiatric disorders
Self-Regulation, Language, and Externalizing Behavior Problems in a Sample of At-Risk Youth: A Social Neuroscience Approach
Behaviors, both positive and negative, are part of a child’s daily social functioning in school, home, and the community. Negative behaviors can impact a child’s social functioning and may lead to referral to a mental health professional. The present study uses the SOCIAL Model to explore the relationship between executive functioning, Broad Reading ability, and teacher-rated externalizing behavior problems and its impact on later social functioning in youth. The data showed teacher-reported conduct problems at were predictive of later discipline infractions and social problems of the student. Teacher-reported peer problems at were not predictive of social problems or discipline infractions. Executive functioning at did not mediate or moderate the relationship between Broad Reading ability at and teacher-reported conduct or peer problems. The results of the current study yield implications for social-emotional screening programs throughout the early elementary school years. Screening during this time period would allow for interventions to occur that may lead to a decline in behavioral difficulties in the classroom, both in elementary school and in high school
Projection to latent spaces disentangles pathological effects on brain morphology in the asymptomatic phase of Alzheimer's disease
Alzheimer's disease (AD) continuum is defined as a cascade of several neuropathological processes that can be measured using biomarkers, such as cerebrospinal fluid (CSF) levels of Aß, p-tau, and t-tau. In parallel, brain anatomy can be characterized through imaging techniques, such as magnetic resonance imaging (MRI). In this work we relate both sets of measurements and seek associations between biomarkers and the brain structure that can be indicative of AD progression. The goal is to uncover underlying multivariate effects of AD pathology on regional brain morphological information. For this purpose, we used the projection to latent structures (PLS) method. Using PLS, we found a low dimensional latent space that best describes the covariance between both sets of measurements on the same subjects. Possible confounder effects (age and sex) on brain morphology are included in the model and regressed out using an orthogonal PLS model. We looked for statistically significant correlations between brain morphology and CSF biomarkers that explain part of the volumetric variance at each region-of-interest (ROI). Furthermore, we used a clustering technique to discover a small set of CSF-related patterns describing the AD continuum. We applied this technique to the study of subjects in the whole AD continuum, from the pre-clinical asymptomatic stages all the way through to the symptomatic groups. Subsequent analyses involved splitting the course of the disease into diagnostic categories: cognitively unimpaired subjects (CU), mild cognitively impaired subjects (MCI), and subjects with dementia (AD-dementia), where all symptoms were due to AD.This work has been partially supported by the project MALEGRA TEC2016-75976-R financed by the Spanish Ministerio de EconomÃa y Competitividad and the European Regional Development Fund (ERDF). AC was supported by the Spanish Ministerio de Educación, Cultura y Deporte FPU Research Fellowship. JG holds a Ramón y Cajal fellowship (RYC-2013-13054).Peer ReviewedPostprint (published version
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The unity and diversity of executive functions: A systematic review and re-analysis of latent variable studies.
Confirmatory factor analysis (CFA) has been frequently applied to executive function measurement since first used to identify a three-factor model of inhibition, updating, and shifting; however, subsequent CFAs have supported inconsistent models across the life span, ranging from unidimensional to nested-factor models (i.e., bifactor without inhibition). This systematic review summarized CFAs on performance-based tests of executive functions and reanalyzed summary data to identify best-fitting models. Eligible CFAs involved 46 samples (N = 9,756). The most frequently accepted models varied by age (i.e., preschool = one/two-factor; school-age = three-factor; adolescent/adult = three/nested-factor; older adult = two/three-factor), and most often included updating/working memory, inhibition, and shifting factors. A bootstrap reanalysis simulated 5,000 samples from 21 correlation matrices (11 child/adolescent; 10 adult) from studies including the three most common factors, fitting seven competing models. Model results were summarized as the mean percent accepted (i.e., average rate at which models converged and met fit thresholds: CFI ≥ .90/RMSEA ≤ .08) and mean percent selected (i.e., average rate at which a model showed superior fit to other models: ΔCFI ≥ .005/.010/ΔRMSEA ≤ -.010/-.015). No model consistently converged and met fit criteria in all samples. Among adult samples, the nested-factor was accepted (41-42%) and selected (8-30%) most often. Among child/adolescent samples, the unidimensional model was accepted (32-36%) and selected (21-53%) most often, with some support for two-factor models without a differentiated shifting factor. Results show some evidence for greater unidimensionality of executive function among child/adolescent samples and both unity and diversity among adult samples. However, low rates of model acceptance/selection suggest possible bias toward the publication of well-fitting but potentially nonreplicable models with underpowered samples. (PsycINFO Database Record (c) 2018 APA, all rights reserved)
Projection to Latent Spaces Disentangles Pathological Effects on Brain Morphology in the Asymptomatic Phase of Alzheimer's Disease
Alzheimer’s disease (AD) continuum is defined as a cascade of several neuropathological
processes that can be measured using biomarkers, such as cerebrospinal fluid (CSF)
levels of Aβ, p-tau, and t-tau. In parallel, brain anatomy can be characterized through
imaging techniques, such as magnetic resonance imaging (MRI). In this work we relate
both sets of measurements and seek associations between biomarkers and the brain
structure that can be indicative of AD progression. The goal is to uncover underlying
multivariate effects of AD pathology on regional brain morphological information. For this
purpose, we used the projection to latent structures (PLS) method. Using PLS, we found
a low dimensional latent space that best describes the covariance between both sets
of measurements on the same subjects. Possible confounder effects (age and sex) on
brain morphology are included in the model and regressed out using an orthogonal PLS
model. We looked for statistically significant correlations between brain morphology and
CSF biomarkers that explain part of the volumetric variance at each region-of-interest
(ROI). Furthermore, we used a clustering technique to discover a small set of CSF-related
patterns describing the AD continuum. We applied this technique to the study of subjects
in the whole AD continuum, from the pre-clinical asymptomatic stages all the way through
to the symptomatic groups. Subsequent analyses involved splitting the course of the
disease into diagnostic categories: cognitively unimpaired subjects (CU), mild cognitively
impaired subjects (MCI), and subjects with dementia (AD-dementia), where all symptoms
were due to AD
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