Associations of screen use with cognitive development in early childhood: the ELFE birth cohort / Shuai YANG in Journal of Child Psychology and Psychiatry, 65-5 (May 2024)  

Public ISBD [article]  inJournal of Child Psychology and Psychiatry > 65-5 (May 2024) . - p.680-693 Titre : Associations of screen use with cognitive development in early childhood: the ELFE birth cohort Type de document : texte imprimé Auteurs : Shuai YANG, Auteur ; Mélèa SAÏD, Auteur ; Hugo PEYRE, Auteur ; Franck RAMUS, Auteur ; Marion TAINE, Auteur ; Evelyn LAW, Auteur ; Marie-Noëlle DUFOURG, Auteur ; Barbara HEUDE, Auteur ; Marie-Aline CHARLES, Auteur ; Jonathan Y. BERNARD, Auteur Article en page(s) : p.680-693 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Background The associations of screen use with children's cognition are not well evidenced and recent, large, longitudinal studies are needed. We aimed to assess the associations between screen use and cognitive development in the French nationwide birth cohort. Methods Time and context of screen use were reported by parents at ages 2, 3.5 and 5.5. Vocabulary, non-verbal reasoning and general cognitive development were assessed with the MacArthur-Bates Communicative Development Inventory (MB) at age 2, the Picture Similarities subtest from the British Ability Scales (PS) at age 3.5 and the Child Development Inventory (CDI) at ages 3.5 and 5.5. Outcome variables were age-adjusted and standardized (mean = 100, SD = 15). Multiple imputations were performed among children (N = 13,763) with 1 screen use information and 1 cognitive measures. Cross-sectional and longitudinal associations between screen use and cognitive development were assessed by linear regression models adjusted for sociodemographic and birth factors related to the family and children, and children's lifestyle factors competing with screen use. Baseline cognitive scores were further considered in longitudinal analysis. Results TV-on during family meals at age 2, not screen time, was associated with lower MB scores at age 2 (? [95% CI] = 1.67 [ 2.21, 1.13]) and CDI scores at age 3.5 ( 0.82 [ 1.31, 0.33]). In cross-sectional analysis, screen time was negatively associated with CDI scores at ages 3.5 ( 0.67 [ 0.94, 0.40]) and 5.5 ( 0.47 [ 0.77, 0.16]), and, in contrast, was positively associated with PS scores (0.39 [0.07, 0.71]) at age 3.5. Screen time at age 3.5 years was not associated with CDI scores at age 5.5 years. Conclusions Our study found weak associations of screen use with cognition after controlling for sociodemographic and children's birth factors and lifestyle confounders, and suggests that the context of screen use matters, not solely screen time, in children's cognitive development. En ligne : https://doi.org/10.1111/jcpp.13887 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=526 [article] Associations of screen use with cognitive development in early childhood: the ELFE birth cohort [texte imprimé] / Shuai YANG, Auteur ; Mélèa SAÏD, Auteur ; Hugo PEYRE, Auteur ; Franck RAMUS, Auteur ; Marion TAINE, Auteur ; Evelyn LAW, Auteur ; Marie-Noëlle DUFOURG, Auteur ; Barbara HEUDE, Auteur ; Marie-Aline CHARLES, Auteur ; Jonathan Y. BERNARD, Auteur . - p.680-693. Langues : Anglais (eng) in Journal of Child Psychology and Psychiatry > 65-5 (May 2024) . - p.680-693 Index. décimale : PER Périodiques Résumé : Background The associations of screen use with children's cognition are not well evidenced and recent, large, longitudinal studies are needed. We aimed to assess the associations between screen use and cognitive development in the French nationwide birth cohort. Methods Time and context of screen use were reported by parents at ages 2, 3.5 and 5.5. Vocabulary, non-verbal reasoning and general cognitive development were assessed with the MacArthur-Bates Communicative Development Inventory (MB) at age 2, the Picture Similarities subtest from the British Ability Scales (PS) at age 3.5 and the Child Development Inventory (CDI) at ages 3.5 and 5.5. Outcome variables were age-adjusted and standardized (mean = 100, SD = 15). Multiple imputations were performed among children (N = 13,763) with 1 screen use information and 1 cognitive measures. Cross-sectional and longitudinal associations between screen use and cognitive development were assessed by linear regression models adjusted for sociodemographic and birth factors related to the family and children, and children's lifestyle factors competing with screen use. Baseline cognitive scores were further considered in longitudinal analysis. Results TV-on during family meals at age 2, not screen time, was associated with lower MB scores at age 2 (? [95% CI] = 1.67 [ 2.21, 1.13]) and CDI scores at age 3.5 ( 0.82 [ 1.31, 0.33]). In cross-sectional analysis, screen time was negatively associated with CDI scores at ages 3.5 ( 0.67 [ 0.94, 0.40]) and 5.5 ( 0.47 [ 0.77, 0.16]), and, in contrast, was positively associated with PS scores (0.39 [0.07, 0.71]) at age 3.5. Screen time at age 3.5 years was not associated with CDI scores at age 5.5 years. Conclusions Our study found weak associations of screen use with cognition after controlling for sociodemographic and children's birth factors and lifestyle confounders, and suggests that the context of screen use matters, not solely screen time, in children's cognitive development. En ligne : https://doi.org/10.1111/jcpp.13887 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=526

Atypical Social Judgment and Sensitivity to Perceptual Cues in Autism Spectrum Disorders / Baudouin FORGEOT D'ARC in Journal of Autism and Developmental Disorders, 46-5 (May 2016)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 46-5 (May 2016) . - p.1574-1581 Titre : Atypical Social Judgment and Sensitivity to Perceptual Cues in Autism Spectrum Disorders Type de document : texte imprimé Auteurs : Baudouin FORGEOT D'ARC, Auteur ; Franck RAMUS, Auteur ; Aline LEFEBVRE, Auteur ; Delphine BROTTIER, Auteur ; Tiziana ZALLA, Auteur ; Sanaa MOUKAWANE, Auteur ; Frédérique AMSELLEM, Auteur ; Laurence LETELLIER, Auteur ; Hugo PEYRE, Auteur ; Marie-Christine MOUREN, Auteur ; Marion LEBOYER, Auteur ; Richard DELORME, Auteur Article en page(s) : p.1574-1581 Langues : Anglais (eng) Mots-clés : Autism  Social judgment  Face processing  Social cognition  Perception Index. décimale : PER Périodiques Résumé : Evaluation of faces is an important dimension of social relationships. A degraded sensitivity to facial perceptual cues might contribute to atypical social interactions in autism spectrum disorder (ASD). The current study investigated whether face based social judgment is atypical in ASD and if so, whether it could be related to a degraded sensitivity to facial perceptual cues. Individuals with ASD (n = 33) and IQ- and age-matched controls (n = 38) were enrolled in this study. Watching a series of photographic or synthetic faces, they had to judge them for “kindness”. In synthetic stimuli, the amount of perceptual cues available could be either large or small. We observed that social judgment was atypical in the ASD group on photographic stimuli, but, contrarily to the prediction based on the degraded sensitivity hypothesis, analyses on synthetic stimuli found a similar performance and a similar effect of the amount of perceptual cues in both groups. Further studies on perceptual differences between photographs and synthetic pictures of faces might help understand atypical social judgment in ASD. En ligne : http://dx.doi.org/10.1007/s10803-014-2208-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=288 [article] Atypical Social Judgment and Sensitivity to Perceptual Cues in Autism Spectrum Disorders [texte imprimé] / Baudouin FORGEOT D'ARC, Auteur ; Franck RAMUS, Auteur ; Aline LEFEBVRE, Auteur ; Delphine BROTTIER, Auteur ; Tiziana ZALLA, Auteur ; Sanaa MOUKAWANE, Auteur ; Frédérique AMSELLEM, Auteur ; Laurence LETELLIER, Auteur ; Hugo PEYRE, Auteur ; Marie-Christine MOUREN, Auteur ; Marion LEBOYER, Auteur ; Richard DELORME, Auteur . - p.1574-1581. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 46-5 (May 2016) . - p.1574-1581 Mots-clés : Autism  Social judgment  Face processing  Social cognition  Perception Index. décimale : PER Périodiques Résumé : Evaluation of faces is an important dimension of social relationships. A degraded sensitivity to facial perceptual cues might contribute to atypical social interactions in autism spectrum disorder (ASD). The current study investigated whether face based social judgment is atypical in ASD and if so, whether it could be related to a degraded sensitivity to facial perceptual cues. Individuals with ASD (n = 33) and IQ- and age-matched controls (n = 38) were enrolled in this study. Watching a series of photographic or synthetic faces, they had to judge them for “kindness”. In synthetic stimuli, the amount of perceptual cues available could be either large or small. We observed that social judgment was atypical in the ASD group on photographic stimuli, but, contrarily to the prediction based on the degraded sensitivity hypothesis, analyses on synthetic stimuli found a similar performance and a similar effect of the amount of perceptual cues in both groups. Further studies on perceptual differences between photographs and synthetic pictures of faces might help understand atypical social judgment in ASD. En ligne : http://dx.doi.org/10.1007/s10803-014-2208-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=288

Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder / Hugo PEYRE in Journal of Child Psychology and Psychiatry, 62-11 (November 2021)  

Public ISBD [article]  inJournal of Child Psychology and Psychiatry > 62-11 (November 2021) . - p.1285-1296 Titre : Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder Type de document : texte imprimé Auteurs : Hugo PEYRE, Auteur ; Tabea SCHOELER, Auteur ; Chaoyu LIU, Auteur ; Camille Michèle WILLIAMS, Auteur ; Nicolas HOERTEL, Auteur ; Alexandra HAVDAHL, Auteur ; Jean-Baptiste PINGAULT, Auteur Article en page(s) : p.1285-1296 Langues : Anglais (eng) Mots-clés : Attention Deficit Disorder with Hyperactivity/epidemiology/genetics  Autism Spectrum Disorder/epidemiology/genetics  Comorbidity  Genome-Wide Association Study  Genomics  Humans  Paired Box Transcription Factors/genetics  Polymorphism, Single Nucleotide  Repressor Proteins/genetics  Autism spectrum disorder  Gwas  Snp  attention deficit hyperactivity disorder  colocalization  common genetic variants  comorbidity  genomic structural equation modelling Index. décimale : PER Périodiques Résumé : BACKGROUND: Attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) are two highly heritable neurodevelopmental disorders. Several lines of evidence point towards the presence of shared genetic factors underlying ASD and ADHD. We conducted genomic analyses of common risk variants (i.e. single nucleotide polymorphisms, SNPs) shared by ASD and ADHD, and those specific to each disorder. METHODS: With the summary data from two GWAS, one on ASD (N = 46,350) and another on ADHD (N = 55,374) individuals, we used genomic structural equation modelling and colocalization analysis to identify SNPs shared by ASD and ADHD and SNPs specific to each disorder. Functional genomic analyses were then conducted on shared and specific common genetic variants. Finally, we performed a bidirectional Mendelian randomization analysis to test whether the shared genetic risk between ASD and ADHD was interpretable in terms of reciprocal relationships between ASD and ADHD. RESULTS: We found that 37.5% of the SNPs associated with ASD (at p < 1e-6) colocalized with ADHD SNPs and that 19.6% of the SNPs associated with ADHD colocalized with ASD SNPs. We identified genes mapped to SNPs that are specific to ASD or ADHD and that are shared by ASD and ADHD, including two novel genes INSM1 and PAX1. Our bidirectional Mendelian randomization analyses indicated that the risk of ASD was associated with an increased risk of ADHD and vice versa. CONCLUSIONS: Using multivariate genomic analyses, the present study uncovers shared and specific genetic variants associated with ASD and ADHD. Further functional investigation of genes mapped to those shared variants may help identify pathophysiological pathways and new targets for treatment. En ligne : http://dx.doi.org/10.1111/jcpp.13479 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=456 [article] Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder [texte imprimé] / Hugo PEYRE, Auteur ; Tabea SCHOELER, Auteur ; Chaoyu LIU, Auteur ; Camille Michèle WILLIAMS, Auteur ; Nicolas HOERTEL, Auteur ; Alexandra HAVDAHL, Auteur ; Jean-Baptiste PINGAULT, Auteur . - p.1285-1296. Langues : Anglais (eng) in Journal of Child Psychology and Psychiatry > 62-11 (November 2021) . - p.1285-1296 Mots-clés : Attention Deficit Disorder with Hyperactivity/epidemiology/genetics  Autism Spectrum Disorder/epidemiology/genetics  Comorbidity  Genome-Wide Association Study  Genomics  Humans  Paired Box Transcription Factors/genetics  Polymorphism, Single Nucleotide  Repressor Proteins/genetics  Autism spectrum disorder  Gwas  Snp  attention deficit hyperactivity disorder  colocalization  common genetic variants  comorbidity  genomic structural equation modelling Index. décimale : PER Périodiques Résumé : BACKGROUND: Attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) are two highly heritable neurodevelopmental disorders. Several lines of evidence point towards the presence of shared genetic factors underlying ASD and ADHD. We conducted genomic analyses of common risk variants (i.e. single nucleotide polymorphisms, SNPs) shared by ASD and ADHD, and those specific to each disorder. METHODS: With the summary data from two GWAS, one on ASD (N = 46,350) and another on ADHD (N = 55,374) individuals, we used genomic structural equation modelling and colocalization analysis to identify SNPs shared by ASD and ADHD and SNPs specific to each disorder. Functional genomic analyses were then conducted on shared and specific common genetic variants. Finally, we performed a bidirectional Mendelian randomization analysis to test whether the shared genetic risk between ASD and ADHD was interpretable in terms of reciprocal relationships between ASD and ADHD. RESULTS: We found that 37.5% of the SNPs associated with ASD (at p < 1e-6) colocalized with ADHD SNPs and that 19.6% of the SNPs associated with ADHD colocalized with ASD SNPs. We identified genes mapped to SNPs that are specific to ASD or ADHD and that are shared by ASD and ADHD, including two novel genes INSM1 and PAX1. Our bidirectional Mendelian randomization analyses indicated that the risk of ASD was associated with an increased risk of ADHD and vice versa. CONCLUSIONS: Using multivariate genomic analyses, the present study uncovers shared and specific genetic variants associated with ASD and ADHD. Further functional investigation of genes mapped to those shared variants may help identify pathophysiological pathways and new targets for treatment. En ligne : http://dx.doi.org/10.1111/jcpp.13479 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=456

Conduites à tenir : Soins psychiatriques aux enfants et adolescents / Hugo PEYRE

Public ISBD in Manuel de psychiatrie / Julien-Daniel GUELFI Titre : Conduites à tenir : Soins psychiatriques aux enfants et adolescents Type de document : texte imprimé Auteurs : Hugo PEYRE, Auteur ; Carmen Maria SCHRODER, Auteur Année de publication : 2021 Importance : p.961-962 Index. décimale : SCI-E SCI-E - Psychiatrie Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=498 in Manuel de psychiatrie / Julien-Daniel GUELFI Conduites à tenir : Soins psychiatriques aux enfants et adolescents [texte imprimé] / Hugo PEYRE, Auteur ; Carmen Maria SCHRODER, Auteur . - 2021 . - p.961-962. Index. décimale : SCI-E SCI-E - Psychiatrie Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=498

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Épidémiologie des troubles de la lecture en France : une comparaison du DSM-5 et de la CIM-11 / Franck RAMUS in Approche Neuropsychologique des Apprentissages chez l'Enfant - A.N.A.E., 175 (Décembre 2021)

Public ISBD [article]  inApproche Neuropsychologique des Apprentissages chez l'Enfant - A.N.A.E. > 175 (Décembre 2021) . - p.639-649 Titre : Épidémiologie des troubles de la lecture en France : une comparaison du DSM-5 et de la CIM-11 Type de document : texte imprimé Auteurs : Franck RAMUS, Auteur ; C. DI FOLCO, Auteur ; A. GUEZ, Auteur ; Hugo PEYRE, Auteur Article en page(s) : p.639-649 Langues : Français (fre) Mots-clés : Trouble de lecture  Prévalence  QI  DSM-5  lCD-1 1 Index. décimale : PER Périodiques Résumé : La présente étude effectue une comparaison systématique entre DSM-5 et CIM-1 1 des critères diagnostiques du trouble de la lecture, dans une population représentative d'élèves français de 6 (n 25000). Elle explore quantitativement les conséquences d'utiliser le DSM-5 ou la CIM-1 1, et des différentes manières d'implémenter chaque critère diagnostique. En utilisant un test de compréhension en lecture pour évaluer les capacités de lecture, un ensemble raisonnable de critères et de seuils aboutit à une prévalence de 6,6 % selon le DSM-5 et de 3,5 % selon la CIM-1 1. Les facteurs qui ont le plus grand impact sur la prévalence sont le critère relatif au décalage entre lecture et 01, et le critère d'interférence avec la performance scolaire. Comparés à la population de référence, les élèves avec trouble de lecture avaient une plus forte probabilité d'être des garçons, d'être en secteur d'éducation prioritaire, et d'avoir des scores plus faibles en niveau socioéconomique, en 01 et en mathématiques. Nos résultats montrent que le choix de classification et la manière précise d'opérationnaliser chaque critère diagnostique peuvent avoir un impact important sur le diagnostic. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=472 [article] Épidémiologie des troubles de la lecture en France : une comparaison du DSM-5 et de la CIM-11 [texte imprimé] / Franck RAMUS, Auteur ; C. DI FOLCO, Auteur ; A. GUEZ, Auteur ; Hugo PEYRE, Auteur . - p.639-649. Langues : Français (fre) in Approche Neuropsychologique des Apprentissages chez l'Enfant - A.N.A.E. > 175 (Décembre 2021) . - p.639-649 Mots-clés : Trouble de lecture  Prévalence  QI  DSM-5  lCD-1 1 Index. décimale : PER Périodiques Résumé : La présente étude effectue une comparaison systématique entre DSM-5 et CIM-1 1 des critères diagnostiques du trouble de la lecture, dans une population représentative d'élèves français de 6 (n 25000). Elle explore quantitativement les conséquences d'utiliser le DSM-5 ou la CIM-1 1, et des différentes manières d'implémenter chaque critère diagnostique. En utilisant un test de compréhension en lecture pour évaluer les capacités de lecture, un ensemble raisonnable de critères et de seuils aboutit à une prévalence de 6,6 % selon le DSM-5 et de 3,5 % selon la CIM-1 1. Les facteurs qui ont le plus grand impact sur la prévalence sont le critère relatif au décalage entre lecture et 01, et le critère d'interférence avec la performance scolaire. Comparés à la population de référence, les élèves avec trouble de lecture avaient une plus forte probabilité d'être des garçons, d'être en secteur d'éducation prioritaire, et d'avoir des scores plus faibles en niveau socioéconomique, en 01 et en mathématiques. Nos résultats montrent que le choix de classification et la manière précise d'opérationnaliser chaque critère diagnostique peuvent avoir un impact important sur le diagnostic. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=472

Fever during pregnancy as a risk factor for neurodevelopmental disorders: results from a systematic review and meta-analysis / Stephanie ANTOUN in Molecular Autism, 12 (2021)  

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Gender differences in autism spectrum disorders: Divergence among specific core symptoms / Anita BEGGIATO in Autism Research, 10-4 (April 2017)  

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Global Sensory Features are Linked to Executive and Attentional Impairments in Autism Spectrum Disorders / Anna MARUANI ; Elise HUMEAU ; Pierre ELLUL ; Ariane CARTIGNY ; Aline LEFEBVRE ; Florine DELLAPIAZZA ; Richard DELORME ; Hugo PEYRE in Journal of Autism and Developmental Disorders, 55-8 (August 2025)  

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Longitudinal change in symptom severity in children with ASD: Results from the ELENA cohort / Florine DELLAPIAZZA in Autism Research, 17-11 (November 2024)  

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Maternal immigrant status and signs of neurodevelopmental problems in early childhood: The French representative ELFE birth cohort / Heiko SCHMENGLER in Autism Research, 12-12 (December)  

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Oculomotor behavior in children with autism spectrum disorders / Simona CALDANI in Autism, 24-3 (April 2020)  

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Regulatory T lymphocytes/Th17 lymphocytes imbalance in autism spectrum disorders: evidence from a meta-analysis / Pierre ELLUL in Molecular Autism, 12 (2021)  

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Spatial and temporal analysis of postural control in children with high functioning Autism Spectrum Disorder / Nathalie GOULÈME in Research in Autism Spectrum Disorders, 40 (August 2017)  

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Trustworthiness and Dominance Personality Traits' Judgments in Adults with Autism Spectrum Disorder / Alice LATIMIER in Journal of Autism and Developmental Disorders, 49-11 (November 2019)  

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