Alexithymia is a multi-faceted construct consisting of: a) difficulties identifying and describing one's emotions, b) difficulty distinguishing emotional feelings from bodily sensations, c) an "externally-oriented thinking style" focused on external realities with limited self-reflective thought towards inner experience, and d) limited imagination and fantasy life (Nemiah et al., 1976).
The present study examined individual differences in theory of mind (ToM) among a group of 60 children (7-11 years-old) with autism spectrum disorder (ASD) and average intelligence. Using open-ended and structured tasks to measure affective ToM, cognitive ToM, and spontaneous social attribution, we explored the nature of ToM and assessed whether ToM predicts the phenotypic heterogeneity in ASD through structural equation modeling. Affective ToM uniquely predicted social symptom severity, whereas no ToM types predicted parent reported social functioning. Our findings suggest that differentiating among theoretical components is crucial for future ToM research in ASD, and ToM challenges related to reasoning about others' emotions may be particularly useful in distinguishing children with worse social symptoms of ASD.
Negative priming provides one useful measure of attentional focus and cognitive control, requirements of most domains of life (driving, work, play, etc.). Until now, 2 types of negative priming have been identified: identity negative priming and location negative priming. These effects are of particular interest because individuals who have difficulty ignoring distraction (e.g., individuals with schizophrenia and attention-deficit disorder) exhibit reduced levels of negative priming. In the present experiments (N = 187), we report an entirely new type of negative priming based on when in time a target appears (temporal negative priming) rather than its identity or spatial location. Results indicate that responses to a target’s temporal position were impaired when a distractor previously appeared at that same relative temporal position. In addition, temporal positioning was teased apart from response-based mechanisms and both were found to independently contribute to temporal negative priming. This result indicates that mechanisms of cognitive control trigger both response-based and memory-based processes.
Autism spectrum disorder (ASD) and schizophrenia spectrum disorder (SCZ) have overlapping symptomatology related to difficulties with social cognition. Yet, few studies have directly compared social cognition in ASD, SCZ, and typical development (TD). The current study examined individual differences in face recognition and its relation to affective theory of mind (ToM) in each diagnostic group. Adults with ASD (n = 31), SCZ (n = 43), and TD (n = 47) between the ages of 18 and 48 years-old with full scale IQ above 80 participated in this study. The Reading the Mind in the Eyes Test (RMET) measured affective ToM, and the Benton Facial Recognition Test (BFRT) measured face perception. Adults with ASD and SCZ did not differ in their affective ToM abilities, and both groups showed affective ToM difficulties compared with TD. However, better face recognition ability uniquely predicted better affective ToM ability in ASD. Results suggest that affective ToM difficulties may relate to face processing in ASD but not SCZ. By clarifying the complex nature of individual differences in affective ToM and face recognition difficulties in these disorders, the present study suggests there may be divergent mechanisms underlying pathways to social dysfunction in ASD compared with SCZ.
Intense interests are common in children with and without autism spectrum disorder (ASD), and little research has characterized aspects of interests that are unique to or shared among children with and without ASD. We aimed to characterize interests in a sample of infants at high‐familial‐risk (HR) and low‐familial‐risk (LR) for ASD using a novel interview. Participants included HR siblings who were diagnosed with ASD at 24 months (HR‐ASD, n = 56), HR siblings who did not receive an ASD diagnosis at 24 months (HR‐Neg, n = 187), and a LR comparison group (n = 109). We developed and collected data with the Intense Interests Inventory at 18‐ and 24‐months of age, a semi‐structured interview that measures intensity and peculiarity of interests in toddlers and preschool‐aged children. Intensity of interests differed by familial risk at 24 months, with HR‐ASD and HR‐Neg groups demonstrating equivalent intensity of interests that were higher than the LR group. By contrast, peculiarity of interest differed by ASD diagnosis, with the HR‐ASD group showing more peculiar interests than the HR‐Neg and LR groups at 24 months. At 18 months the HR‐ASD group had more peculiar interests than the LR group, though no differences emerged in intensity of interests. This measure may be useful in identifying clinically‐relevant features of interests in young children with ASD. We also replicated previous findings of males showing more intense interests at 18 months in our non‐ASD sample. These results reveal new information about the nature of interests and preoccupations in the early autism phenotype.
Lay summary
Intense interests are common in young children with autism and their family members. Intense interests are also prevalent among typically‐developing children, and especially boys. Here we catalog interests and features of these interests in a large sample of toddlers enriched for autism risk. Children who had family members with autism had more intense interests, and those who developed autism themselves had more unusual interests at 24 months. These results highlight the importance of different aspects of interest in autism.
Traditional categorical approaches to classifying personality disorders are limited in important ways, leading to a shift in the field to dimensional approaches to conceptualizing personality pathology. Different areas of psychology – personality, developmental, and psychopathology – can be leveraged to understand personality pathology by examining its structure, development, and underlying mechanisms. However, an integrative model that encompasses these distinct lines of inquiry has not yet been proposed. In order to address this gap, we review the latest evidence for dimensional classification of personality disorders based on structural models of maladaptive personality traits, provide an overview of developmental theories of pathological personality, and summarize the Research Domain Criteria (RDoC) initiative, which seeks to understand underlying mechanisms of psychopathology. We conclude by proposing an integrative model of personality pathology development that aims to elucidate the developmental pathways of personality pathology and its underlying mechanisms.
Background
The Social Communication Questionnaire (SCQ) is a screening checklist for autism spectrum disorder (ASD) commonly used in research and clinical practice. While the original validation study suggested that the SCQ was an accurate ASD screener with satisfactory sensitivity and specificity, subsequent studies have yielded mixed results, with some revealing low sensitivity, low specificity, and low utility as a screening tool. However, it is unknown for whom the SCQ is effective versus ineffective as a screening tool.
Method
The present study examined the psychometric properties of the SCQ as well as the individual difference characteristics of 187 individuals with and without autism spectrum disorder (ASD) who were misclassified or accurately classified by the SCQ in a clinical-referred sample.
Results
The SCQ showed suboptimal sensitivity and specificity, regardless of age and sex. Compared to true positives, individuals classified as false positives displayed greater externalizing and internalizing problems, whereas individuals classified as false negatives displayed better social communication and adaptive skills.
Conclusions
The findings suggest non-autistic developmental and behavioral individual difference characteristics may explain high rates of misclassification using the SCQ. The SCQ may be less useful as a screener for young children with internalizing and externalizing symptoms and other more complex clinical presentations.
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