21 research outputs found

    Does Mind-Wandering Relate to Mood and Stress in Young Adults? A Narrative Review

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    Mind-wandering (MW) is ubiquitous and has been extensively studied in young adults. Studies have shown that MW, daydreaming, and sluggish cognitive tempo symptoms (SCT; e.g., staring, mental fogginess, confusion, hypoactivity, sluggishness, lethargy, and drowsiness) are interrelated constructs and all relate to mood and stress-related symptoms. The aims of the current review are to a) document the associations between MW (and related constructs: daydreaming, and SCT) and mood/stress-related symptoms (e.g., anxiety and depression symptoms) in young adults and b) identify potential mechanisms underlying these relationships. We conducted a narrative review of the literature on the subject. We searched MEDLINE (Ovid) and PsycINFO® (Ovid) databases and performed duplicate and independent screening. A total of 559 unique records were identified, and 22 records (published between 1978 and 2017) were included. We confirmed existing evidence of the associations between MW, daydreaming, SCT and mood/stress-related symptoms in young adults (aged 18 - 30 years). Although these associations are reported, our understanding of its directionality and underlying mechanisms remains incomplete. These findings highlight the need for further research combining experimental and correlational designs and including possible mechanisms of these associations in this population

    Étiologie génétique et cognitive de l'association entre les habiletés en lecture et les dimensions du trouble déficitaire de l'attention avec ou sans hyperactivité (TDAH)

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    Tableau d'honneur de la Faculté des études supérieures et postdoctorales, 2016-2017La présente thèse examine les associations entre les dimensions du TDAH et les habiletés en lecture sur les plans phénotypique, génétique et cognitif. En premier lieu, les associations entre les dimensions du TDAH (inattention et hyperactivité/impulsivité) et les habiletés en lecture (décodage et compréhension en lecture) chez des enfants au début du primaire (6-8 ans) ont été examinées. Les résultats révèlent des associations similaires. Toutefois, seules celles entre l’inattention et les habiletés en lecture demeurent après que l’hyperactivité/impulsivité, les symptômes de trouble du comportement et les habiletés non verbales aient été contrôlés. De plus, les associations entre l’inattention et les habiletés en lecture s’expliquent en grande partie par des facteurs génétiques. En second lieu, les associations entre les dimensions du TDAH et les habiletés en lecture (lecture de mots et exactitude/vitesse lors de la lecture d’un texte) ont été étudiées à 14-15 ans. Seule l’inattention demeure associée aux habiletés en lecture après que l’hyperactivité/impulsivité, les habiletés verbales et les habiletés non verbales aient été contrôlées. L’inattention et les habiletés en lecture sont aussi corrélées sur le plan génétique, mais ces corrélations deviennent non significatives lorsque les habiletés verbales sont contrôlées. En dernier lieu, des habiletés cognitives ont été étudiées comme mécanismes sous-jacents potentiels de l’association entre l’inattention et les habiletés en lecture (décodage et compréhension en lecture) à l’enfance. Il apparait que la conscience phonologique, la vitesse de dénomination de chiffres, le traitement temporel bimodal et le vocabulaire sont des médiateurs de l’association entre l’inattention et le décodage alors que la conscience phonologique, la vitesse de dénomination de chiffres et de couleurs et le vocabulaire sont des médiateurs de l’association entre l’inattention et la compréhension en lecture. De plus, des facteurs génétiques communs ont été observés entre certains médiateurs (conscience phonologique, vitesse de dénomination des chiffres et traitement temporel bimodal), l’inattention et le décodage. Somme toute, la présente thèse montre que des facteurs génétiques expliquent en partie ces associations à l’enfance et l’adolescence. Des médiateurs cognitifs sous-tendent ces associations, possiblement par des processus génétiques et environnementaux qui devront être précisés dans le futur.The present thesis investigates the associations between ADHD dimensions and reading abilities on phenotypic, genetic, and cognitive levels. First, the associations between ADHD dimensions (inattention and hyperactivity/impulsivity) and reading abilities (decoding skills and reading comprehension) in early primary school (6-8 years old) have been documented. Results showed that these associations are similar. However, only the associations between inattention and both reading abilities remain after controlling for hyperactivity/impulsivity, behaviour disorder symptoms, and nonverbal abilities. Moreover, these associations are mostly explained by genetic factors. Second, the associations between ADHD dimensions and reading abilities (word reading, accuracy and speed of text reading) have been studied during adolescence (14-15 years old). Only inattention is associated with reading abilities, after controlling for hyperactivity/impulsivity, verbal abilities, and nonverbal abilities. Inattention is genetically correlated with reading abilities, but these genetic correlations become not significant when verbal abilities are controlled. Finally, some cognitive skills have been studied as potential underlying mechanisms of the associations between inattention and reading abilities (decoding and reading comprehension) during childhood. Phonological awareness, rapid automatized naming (RAN) of numbers, bimodal rapid processing, and vocabulary are mediators of the association between inattention and decoding skills while phonological awareness, RAN of numbers and colours, and vocabulary are mediators of the association between inattention and reading comprehension. Moreover, there are common genetic factors between some cognitive skills (phonological awareness, RAN of numbers, bimodal rapid processing), inattention, and decoding skills. In sum, the present thesis shows that genetic factors partially explain these associations during childhood and adolescence. Cognitive mediators underlie these associations, potentially by genetic and environmental factors that will need to be specified in future studies

    Phenotypic and genetic associations between reading comprehension, decoding skills, and ADHD dimensions : evidence from two population-based studies

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    BACKGROUND: The phenotypic and genetic associations between decoding skills and ADHD dimensions have been documented but less is known about the association with reading comprehension. The aim of the study is to document the phenotypic and genetic associations between reading comprehension and ADHD dimensions of inattention and hyperactivity/impulsivity in early schooling and compare them to those with decoding skills. METHODS: Data were collected in two population-based samples of twins (Quebec Newborn Twin Study - QNTS) and singletons (Quebec Longitudinal Study of Child Development - QLSCD) totaling ≈ 2300 children. Reading was assessed with normed measures in second or third grade. Teachers assessed ADHD dimensions in kindergarten and first grade. RESULTS: Both decoding and reading comprehension were correlated with ADHD dimensions in a similar way: associations with inattention remained after controlling for the other ADHD dimension, behavior disorder symptoms and nonverbal abilities, whereas associations with hyperactivity/impulsivity did not. Genetic modeling showed that decoding and comprehension largely shared the same genetic etiology at this age and that their associations with inattention were mostly explained by shared genetic influences. CONCLUSION: Both reading comprehension and decoding are uniquely associated with inattention through a shared genetic etiology

    Complex effects of dyslexia risk factors account for ADHD-traits : evidence from two independent samples

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    Background: Developmental dyslexia (DD) and attention deficit/hyperactivity disorder (ADHD) are among the most common neurodevelopmental disorders, whose etiology involves multiple risk factors. DD and ADHD co-occur in the same individuals much more often than would be expected by chance. Several studies have found significant bivariate heritability, and specific genes associated with either DD or ADHD have been investigated for association in the other disorder. Moreover, there are likely to be gene-by-gene and gene-by-environment interaction effects (GxG and GxE, respectively) underlying the comorbidity between DD and ADHD. We investigated the pleiotropic effects of 19 SNPs spanning five DD genes (DYX1C1, DCDC2, KIAA0319, ROBO1 and GRIN2B) and seven DD environmental factors (smoke, miscarriage, birth weight, breastfeeding, parental age, socioeconomic status and parental education) for main, either 1) genetic or 2) environmental, 3) G×G, and 4) G×E upon inattention and hyperactivity/impulsivity. We then attempted replication of these findings in an independent twin cohort. Methods: Marker-trait association was analyzed by implementing the Quantitative Transmission Disequilibrium Test (QTDT). Environmental associations were tested by partial correlations. GxG were investigated by a general linear model equation and a family-based association test. GxE were analyzed through a general test for GxE in sib-pair-based association analysis of quantitative traits. Results: DCDC2-rs793862 was associated with hyperactivity/impulsivity via G×G (KIAA0319) and G×E (miscarriage). Smoke was significantly correlated with hyperactivity/impulsivity. We replicated the DCDC2×KIAA0319 interaction upon hyperactivity/impulsivity in the twin cohort. Conclusions: DD genetic (DCDC2) and environmental factors (smoke and miscarriage) underlie ADHD-traits supporting a potential pleiotropic effect

    Parental Knowledge, Self-confidence, and Usability Evaluation of a Web-Based Infographic for Pediatric Concussion: Multimethod Study

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    BackgroundConcussions, which are known as mild traumatic brain injuries, are complex injuries caused by direct or indirect blows to the head and are increasingly being recognized as a significant public health concern for children and their families. Previous research has identified few studies examining the efficacy of educational interventions on parental concussion knowledge. The aim of this research was to actively work together with children who have experienced a concussion and their parents to develop, refine, and evaluate the usability of a web-based infographic for pediatric concussion. ObjectiveThe objective of this study was to report on the usability of the infographic, parental knowledge, and self-confidence in pediatric concussion knowledge before and after exposure to the infographic. MethodsA multiphase, multimethod research design using patient engagement techniques was used to develop a web-based infographic. For this phase of the research (usability, knowledge, and confidence evaluation), parents who could communicate in English were recruited via social media platforms and invited to complete web-based questionnaires. Electronic preintervention and postintervention questionnaires were administered to parents to assess changes to concussion knowledge and confidence after viewing the infographic. A usability questionnaire with 11 items was also completed. ResultsA web-based, infographic was developed. The infographic is intended for parents and children and incorporates information that parents and children identified as both wants and needs about concussion alongside the best available research evidence on pediatric concussion. A total of 31 surveys were completed by parents. The mean scores for each item on the usability surveys ranged from 8.03 (SD 1.70) to 9.26 (SD 1.09) on a 10-point Likert scale, indicating that the usability components of the infographic were largely positive. There was no statistically significant difference between preintervention and postintervention knowledge scores (Z=−0.593; P=.55; both preintervention and postintervention knowledge scores had a median of 9 out of 10). In contrast, there was a statistically significant difference between preintervention (mean 3.9/5, SD 0.56) and postintervention (mean 4.4/5, SD 0.44) confidence in knowledge scores (t30=−5.083; P<.001). ConclusionsOur results demonstrate that parents positively rated a web-based, infographic for pediatric concussion. In addition, although there was no statistically significant difference overall in parents’ knowledge scores before and after viewing the infographic, their confidence in their knowledge did significantly increase. These results suggest that using a web-based infographic as a knowledge translation intervention may be useful in increasing parents’ confidence in managing their child’s concussion

    Comparison of measures of morphosyntactic complexity in French-speaking school-aged children

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    This study examined the validity and reliability of different measures of morphosyntactic complexity, including the Morphosyntactic Complexity Scale (MSCS), a novel adaptation of the Developmental Sentence Scoring, in French-speaking school-aged children. Seventy-three Quebec children from kindergarten to Grade 3 completed a definition task and a narration task. Mean length of utterance (MLU), clause density and MSCS global score, average frequency scores and average complexity scores were calculated from the transcripts of the two contexts. MLU, clause density and MSCS global score were correlated with vocabulary knowledge and narrative skills, and they increased as a function of school level, suggesting that they are valid measures of morphosyntactic complexity. Moreover, the three scores were correlated across contexts, suggesting that they are also reliable measures. However, no MSCS average frequency or average complexity score was found to be both valid and reliable. These findings will guide researchers and practitioners who desire to assess the language skills of French-speaking school-aged children

    Phenotypic and genetic associations between reading and attention-deficit/hyperactivity disorder dimensions in adolescence

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    Multiple studies have shown that reading abilities and attention-deficit/hyperactivity disorder symptoms, mainly inattention symptoms, are phenotypically and genetically associated during childhood. However, few studies have looked at these associations during adolescence to investigate possible developmental changes. The aim of the study is to examine the genetic and environmental etiology of the associations between inattention and hyperactivity reported by parents, and reading accuracy, reading speed, and word reading in a population-based twin sample (Quebec Newborn Twin Study). Participants were between 14 and 15 years of age at the time of testing (N = 668-837). Phenotypic results showed that when nonverbal and verbal abilities were controlled, inattention, but not hyperactivity/impulsivity, was a modest and significant predictor of reading accuracy, reading speed, and word reading. The associations between inattention and all reading abilities were partly explained by genetic and unique environmental factors. However, the genetic correlations were no longer significant after controlling for verbal abilities. In midadolescence, inattention is the attention-deficit/hyperactivity disorder dimension associated with reading abilities, but they could also share genetic factors with general verbal skills

    Phenotypic and genetic associations between reading and attention-deficit/hyperactivity disorder dimensions in adolescence

    No full text
    Multiple studies have shown that reading abilities and attention-deficit/hyperactivity disorder symptoms, mainly inattention symptoms, are phenotypically and genetically associated during childhood. However, few studies have looked at these associations during adolescence to investigate possible developmental changes. The aim of the study is to examine the genetic and environmental etiology of the associations between inattention and hyperactivity reported by parents, and reading accuracy, reading speed, and word reading in a population-based twin sample (Quebec Newborn Twin Study). Participants were between 14 and 15 years of age at the time of testing (N = 668–837). Phenotypic results showed that when nonverbal and verbal abilities were controlled, inattention, but not hyperactivity/impulsivity, was a modest and significant predictor of reading accuracy, reading speed, and word reading. The associations between inattention and all reading abilities were partly explained by genetic and unique environmental factors. However, the genetic correlations were no longer significant after controlling for verbal abilities. In midadolescence, inattention is the attention-deficit/hyperactivity disorder dimension associated with reading abilities, but they could also share genetic factors with general verbal skills

    Phenotypic and genetic associations between reading and attention-deficit/hyperactivity disorder dimensions in adolescence

    No full text
    Multiple studies have shown that reading abilities and attention-deficit/hyperactivity disorder symptoms, mainly inattention symptoms, are phenotypically and genetically associated during childhood. However, few studies have looked at these associations during adolescence to investigate possible developmental changes. The aim of the study is to examine the genetic and environmental etiology of the associations between inattention and hyperactivity reported by parents, and reading accuracy, reading speed, and word reading in a population-based twin sample (Quebec Newborn Twin Study). Participants were between 14 and 15 years of age at the time of testing (N = 668–837). Phenotypic results showed that when nonverbal and verbal abilities were controlled, inattention, but not hyperactivity/impulsivity, was a modest and significant predictor of reading accuracy, reading speed, and word reading. The associations between inattention and all reading abilities were partly explained by genetic and unique environmental factors. However, the genetic correlations were no longer significant after controlling for verbal abilities. In midadolescence, inattention is the attention-deficit/hyperactivity disorder dimension associated with reading abilities, but they could also share genetic factors with general verbal skills
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