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The possible involvement of genetic variants of NET1 in the etiology of attention-deficit/hyperactivity disorder comorbid with oppositional defiant disorder / Lu LIU in Journal of Child Psychology and Psychiatry, 56-1 (January 2015)
[article]
Titre : The possible involvement of genetic variants of NET1 in the etiology of attention-deficit/hyperactivity disorder comorbid with oppositional defiant disorder Type de document : Texte imprimé et/ou numérique Auteurs : Lu LIU, Auteur ; Jia CHENG, Auteur ; Haimei LI, Auteur ; Li YANG, Auteur ; Qiujin QIAN, Auteur ; Yufeng WANG, Auteur Article en page(s) : p.58-66 Langues : Anglais (eng) Mots-clés : ADHD ODD NET1 association Index. décimale : PER Périodiques Résumé : Background Attention-deficit/hyperactivity disorder (ADHD) and oppositional defiant disorder (ODD) often coexist and shared some genetic influences. Evidence from the existing literature indicated that comorbid with ODD may increase the heterogeneity of ADHD genetics. Our present study sought to investigate the role of norepinephrine transporter gene (NET1) for ADHD comorbid with ODD. Methods Six single nucleotide polymorphisms (SNPs) of NET1 were genotyped for a total of 1,815 ADHD cases, including 587 subjects (32.3%) with ODD. Chi-square tests were conducted for pseudo case–control study comparing allelic and genotypic distributions between ADHD with and without ODD. Among them, there were 1,249 probands together with their parents composing trios for family-based association studies using transmission disequilibrium tests (TDTs). In addition, 1,337 ADHD probands have detailed information of ODD symptoms and were included for quantitative analyses with genotypes using analyses of covariance (ANCOVA). To consider the overlap and correlation of other comorbidities with ODD and eliminate their potential confounding effect, we further repeated above analyses for ‘pure ADHD+ODD’ versus ‘ADHD-only’ after excluding other comorbidities except for ODD. Results The pseudo case–control study showed different allelic and genotypic distributions of SNP rs3785143 between ADHD with ODD and those without ODD. Family-based association tests indicated overtransmission of the T allele of rs3785143 in ADHD with ODD trios, but no biased transmission in those without ODD. ANCOVA showed association between genotypes of rs3785143 with ODD symptoms in ADHD probands, especially with ‘Argumentative/Defiant Behavior (ADB)’ dimension after controlling gender, age, clinical subtypes and intelligence. Above association still existed after removing the samples with other comorbidities. Conclusion NET1 was associated with comorbidity of ODD and ODD symptoms in ADHD probands. Our findings emphasize the importance of considering the comorbidity of ODD in ADHD genetic studies, especially ADHD with ADB. However, further replication in independent sample or different populations is still needed. En ligne : http://dx.doi.org/10.1111/jcpp.12278 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=259
in Journal of Child Psychology and Psychiatry > 56-1 (January 2015) . - p.58-66[article] The possible involvement of genetic variants of NET1 in the etiology of attention-deficit/hyperactivity disorder comorbid with oppositional defiant disorder [Texte imprimé et/ou numérique] / Lu LIU, Auteur ; Jia CHENG, Auteur ; Haimei LI, Auteur ; Li YANG, Auteur ; Qiujin QIAN, Auteur ; Yufeng WANG, Auteur . - p.58-66.
Langues : Anglais (eng)
in Journal of Child Psychology and Psychiatry > 56-1 (January 2015) . - p.58-66
Mots-clés : ADHD ODD NET1 association Index. décimale : PER Périodiques Résumé : Background Attention-deficit/hyperactivity disorder (ADHD) and oppositional defiant disorder (ODD) often coexist and shared some genetic influences. Evidence from the existing literature indicated that comorbid with ODD may increase the heterogeneity of ADHD genetics. Our present study sought to investigate the role of norepinephrine transporter gene (NET1) for ADHD comorbid with ODD. Methods Six single nucleotide polymorphisms (SNPs) of NET1 were genotyped for a total of 1,815 ADHD cases, including 587 subjects (32.3%) with ODD. Chi-square tests were conducted for pseudo case–control study comparing allelic and genotypic distributions between ADHD with and without ODD. Among them, there were 1,249 probands together with their parents composing trios for family-based association studies using transmission disequilibrium tests (TDTs). In addition, 1,337 ADHD probands have detailed information of ODD symptoms and were included for quantitative analyses with genotypes using analyses of covariance (ANCOVA). To consider the overlap and correlation of other comorbidities with ODD and eliminate their potential confounding effect, we further repeated above analyses for ‘pure ADHD+ODD’ versus ‘ADHD-only’ after excluding other comorbidities except for ODD. Results The pseudo case–control study showed different allelic and genotypic distributions of SNP rs3785143 between ADHD with ODD and those without ODD. Family-based association tests indicated overtransmission of the T allele of rs3785143 in ADHD with ODD trios, but no biased transmission in those without ODD. ANCOVA showed association between genotypes of rs3785143 with ODD symptoms in ADHD probands, especially with ‘Argumentative/Defiant Behavior (ADB)’ dimension after controlling gender, age, clinical subtypes and intelligence. Above association still existed after removing the samples with other comorbidities. Conclusion NET1 was associated with comorbidity of ODD and ODD symptoms in ADHD probands. Our findings emphasize the importance of considering the comorbidity of ODD in ADHD genetic studies, especially ADHD with ADB. However, further replication in independent sample or different populations is still needed. En ligne : http://dx.doi.org/10.1111/jcpp.12278 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=259 The possible role of the kynurenine pathway in adolescent depression with melancholic features / Vilma GABBAY in Journal of Child Psychology and Psychiatry, 51-8 (August 2010)
[article]
Titre : The possible role of the kynurenine pathway in adolescent depression with melancholic features Type de document : Texte imprimé et/ou numérique Auteurs : Vilma GABBAY, Auteur ; Rachel G. KLEIN, Auteur ; Yisrael KATZ, Auteur ; Sandra MENDOZA, Auteur ; Leah E. GUTTMAN, Auteur ; Carmen M. ALONSO, Auteur ; James S. BABB, Auteur ; Glenn S. HIRSCH, Auteur ; Leonard LIEBES, Auteur Année de publication : 2010 Article en page(s) : p.935-943 Langues : Anglais (eng) Mots-clés : Adolescent-depression indoleamine dioxygenase IDO kynurenine-(KYN) tryptophan(TRP) melancholic MDD subtypes Index. décimale : PER Périodiques Résumé : Background: Although adolescent major depressive disorder (MDD) is acknowledged to be a heterogeneous disorder, no studies have reported on biological correlates of its clinical subgroups. This study addresses this issue by examining whether adolescent MDD with and without melancholic features (M-MDD and NonM-MDD) have distinct biological features in the kynurenine pathway (KP). The KP is initiated by pro-inflammatory cytokines via induction of the enzyme indoleamine 2,3-dioxygenase (IDO), which degrades tryptophan (TRP) into kynurenine (KYN). KYN is further metabolized into neurotoxins linked to neuronal dysfunction in MDD. Hypotheses were that, compared to healthy controls and to NonM-MDD adolescents, adolescents with M-MDD would exhibit: (i) increased activation of the KP [i.e., increased KYN and KYN/TRP (reflecting IDO activity)]; (ii) greater neurotoxic loads [i.e., increased 3-hydroxyanthranilic acid (3-HAA, neurotoxin) and 3-HAA/KYN (reflecting production of neurotoxins)]; and (iii) decreased TRP. We also examined relationships between severity of MDD and KP metabolites.
Methods: Subjects were 20 adolescents with M-MDD, 30 adolescents with NonM-MDD, and 22 healthy adolescents. MDD episode duration had to be ≥ 6 weeks and Children’s Depression Rating Scale-Revised (CDRS-R) scores were ≥ 36. Blood samples were collected at AM after an overnight fast and analyzed using high-performance liquid chromatography. Group contrasts relied on analysis of covariance based on ranks, adjusted for age, gender, and CDRS-R scores. Analyses were repeated excluding medicated patients. Fisher’s protected least significant difference was used for multiple comparisons.
Results: As hypothesized, KYN/TRP ratios were elevated and TRP concentrations were reduced in adolescents with M-MDD compared to NonM-MDD adolescents (p = .001 and .006, respectively) and to healthy controls (p = .008 and .022, respectively). These findings remained significant when medicated patients were excluded from the analyses. Significant correlations were obtained exclusively in the M-MDD group between KYN and 3-HAA/KYN and CDRS-R.
Conclusions: Findings support the notion that adolescent M-MDD may represent a biologically distinct clinical syndrome.En ligne : http://dx.doi.org/10.1111/j.1469-7610.2010.02245.x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=108
in Journal of Child Psychology and Psychiatry > 51-8 (August 2010) . - p.935-943[article] The possible role of the kynurenine pathway in adolescent depression with melancholic features [Texte imprimé et/ou numérique] / Vilma GABBAY, Auteur ; Rachel G. KLEIN, Auteur ; Yisrael KATZ, Auteur ; Sandra MENDOZA, Auteur ; Leah E. GUTTMAN, Auteur ; Carmen M. ALONSO, Auteur ; James S. BABB, Auteur ; Glenn S. HIRSCH, Auteur ; Leonard LIEBES, Auteur . - 2010 . - p.935-943.
Langues : Anglais (eng)
in Journal of Child Psychology and Psychiatry > 51-8 (August 2010) . - p.935-943
Mots-clés : Adolescent-depression indoleamine dioxygenase IDO kynurenine-(KYN) tryptophan(TRP) melancholic MDD subtypes Index. décimale : PER Périodiques Résumé : Background: Although adolescent major depressive disorder (MDD) is acknowledged to be a heterogeneous disorder, no studies have reported on biological correlates of its clinical subgroups. This study addresses this issue by examining whether adolescent MDD with and without melancholic features (M-MDD and NonM-MDD) have distinct biological features in the kynurenine pathway (KP). The KP is initiated by pro-inflammatory cytokines via induction of the enzyme indoleamine 2,3-dioxygenase (IDO), which degrades tryptophan (TRP) into kynurenine (KYN). KYN is further metabolized into neurotoxins linked to neuronal dysfunction in MDD. Hypotheses were that, compared to healthy controls and to NonM-MDD adolescents, adolescents with M-MDD would exhibit: (i) increased activation of the KP [i.e., increased KYN and KYN/TRP (reflecting IDO activity)]; (ii) greater neurotoxic loads [i.e., increased 3-hydroxyanthranilic acid (3-HAA, neurotoxin) and 3-HAA/KYN (reflecting production of neurotoxins)]; and (iii) decreased TRP. We also examined relationships between severity of MDD and KP metabolites.
Methods: Subjects were 20 adolescents with M-MDD, 30 adolescents with NonM-MDD, and 22 healthy adolescents. MDD episode duration had to be ≥ 6 weeks and Children’s Depression Rating Scale-Revised (CDRS-R) scores were ≥ 36. Blood samples were collected at AM after an overnight fast and analyzed using high-performance liquid chromatography. Group contrasts relied on analysis of covariance based on ranks, adjusted for age, gender, and CDRS-R scores. Analyses were repeated excluding medicated patients. Fisher’s protected least significant difference was used for multiple comparisons.
Results: As hypothesized, KYN/TRP ratios were elevated and TRP concentrations were reduced in adolescents with M-MDD compared to NonM-MDD adolescents (p = .001 and .006, respectively) and to healthy controls (p = .008 and .022, respectively). These findings remained significant when medicated patients were excluded from the analyses. Significant correlations were obtained exclusively in the M-MDD group between KYN and 3-HAA/KYN and CDRS-R.
Conclusions: Findings support the notion that adolescent M-MDD may represent a biologically distinct clinical syndrome.En ligne : http://dx.doi.org/10.1111/j.1469-7610.2010.02245.x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=108 The Potential Effectiveness of Social Skills Groups for Adults with Autism / Patricia HOWLIN in Autism, 3-3 (September 1999)
[article]
Titre : The Potential Effectiveness of Social Skills Groups for Adults with Autism Type de document : Texte imprimé et/ou numérique Auteurs : Patricia HOWLIN, Auteur ; Pamela YATES, Auteur Article en page(s) : p.299-307 Langues : Anglais (eng) Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1177/1362361399003003007 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=208
in Autism > 3-3 (September 1999) . - p.299-307[article] The Potential Effectiveness of Social Skills Groups for Adults with Autism [Texte imprimé et/ou numérique] / Patricia HOWLIN, Auteur ; Pamela YATES, Auteur . - p.299-307.
Langues : Anglais (eng)
in Autism > 3-3 (September 1999) . - p.299-307
Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1177/1362361399003003007 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=208 The potential role for emergence in autism / George M. ANDERSON in Autism Research, 1-1 (February 2008)
[article]
Titre : The potential role for emergence in autism Type de document : Texte imprimé et/ou numérique Auteurs : George M. ANDERSON, Auteur Année de publication : 2008 Article en page(s) : p.18-30 Langues : Anglais (eng) Mots-clés : autism emergence emergent dimensional fractionable intellectual-disability epilepsy Index. décimale : PER Périodiques Résumé : Although most research on autistic behavior has considered autism categorically, the increasingly apparent genetic and phenotypic complexities of autism are prompting a more dimensional approach to this area. The long-standing interest in a less categorical approach is made clear from a review of literature. The accumulating empirical support for viewing autism-related phenomena as separable and fractionable is outlined and includes data indicating that many of the behaviors occur in isolation in family members and the general population, are not highly correlated within individuals, and appear to be inherited separately. However, it is emphasized that some of the most common and characteristic phenomena observed in individuals diagnosed with autism do not run in their families. It is suggested that these novel, emergent, phenomena may arise in the individual from interacting configurations of co-occurring traits or from the interaction of genetic and biological factors underlying the traits. A number of autism-related phenomena including intellectual disability, seizures, persistence of primitive reflexes, stereotypies, self-injurious behavior, savant abilities, and morphological abnormalities, among others, are discussed as potentially being emergent. It is concluded that consideration of the role of emergence in autistic behavior and related phenomena should complement a reductionist approach and might help illuminate the components and complexities of autism. En ligne : http://dx.doi.org/10.1002/aur.2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=929
in Autism Research > 1-1 (February 2008) . - p.18-30[article] The potential role for emergence in autism [Texte imprimé et/ou numérique] / George M. ANDERSON, Auteur . - 2008 . - p.18-30.
Langues : Anglais (eng)
in Autism Research > 1-1 (February 2008) . - p.18-30
Mots-clés : autism emergence emergent dimensional fractionable intellectual-disability epilepsy Index. décimale : PER Périodiques Résumé : Although most research on autistic behavior has considered autism categorically, the increasingly apparent genetic and phenotypic complexities of autism are prompting a more dimensional approach to this area. The long-standing interest in a less categorical approach is made clear from a review of literature. The accumulating empirical support for viewing autism-related phenomena as separable and fractionable is outlined and includes data indicating that many of the behaviors occur in isolation in family members and the general population, are not highly correlated within individuals, and appear to be inherited separately. However, it is emphasized that some of the most common and characteristic phenomena observed in individuals diagnosed with autism do not run in their families. It is suggested that these novel, emergent, phenomena may arise in the individual from interacting configurations of co-occurring traits or from the interaction of genetic and biological factors underlying the traits. A number of autism-related phenomena including intellectual disability, seizures, persistence of primitive reflexes, stereotypies, self-injurious behavior, savant abilities, and morphological abnormalities, among others, are discussed as potentially being emergent. It is concluded that consideration of the role of emergence in autistic behavior and related phenomena should complement a reductionist approach and might help illuminate the components and complexities of autism. En ligne : http://dx.doi.org/10.1002/aur.2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=929 The potential role of insulin-like growth factor-1 and zinc in brain growth of autism spectrum disorder children / R. B. KHALIL in Autism, 23-1 (January 2019)
[article]
Titre : The potential role of insulin-like growth factor-1 and zinc in brain growth of autism spectrum disorder children Type de document : Texte imprimé et/ou numérique Auteurs : R. B. KHALIL, Auteur Article en page(s) : p.267-268 Langues : Anglais (eng) Mots-clés : Psychology Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1177/1362361317753565 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=379
in Autism > 23-1 (January 2019) . - p.267-268[article] The potential role of insulin-like growth factor-1 and zinc in brain growth of autism spectrum disorder children [Texte imprimé et/ou numérique] / R. B. KHALIL, Auteur . - p.267-268.
Langues : Anglais (eng)
in Autism > 23-1 (January 2019) . - p.267-268
Mots-clés : Psychology Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1177/1362361317753565 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=379 The potential role of a retrotransposed gene and a long noncoding RNA in regulating an X-linked chromatin gene (KDM5C): Novel epigenetic mechanism in autism / Zohreh TALEBIZADEH in Autism Research, 12-7 (July 2019)
PermalinkThe Power of Positivity: Predictors of Relationship Satisfaction for Parents of Children with Autism Spectrum Disorder / Naomi V. EKAS in Journal of Autism and Developmental Disorders, 45-7 (July 2015)
PermalinkThe power of words: Is qualitative research as important as quantitative research in the study of autism? / Sven BÖLTE in Autism, 18-2 (February 2014)
PermalinkThe predictive capacity of psychiatric and psychological polygenic risk scores for distinguishing cases in a child and adolescent psychiatric sample from controls / A. G. JANSEN in Journal of Child Psychology and Psychiatry, 62-9 (September 2021)
PermalinkThe Predictive Relationship Between Sensory Reactivity and Depressive Symptoms in Young Autistic Children with Few to No Words / Timothy Rossow ; Keren MACLENNAN ; Teresa TAVASSOLI in Journal of Autism and Developmental Disorders, 53-6 (June 2023)
PermalinkThe predictive significance of early caregiving experiences for symptoms of psychopathology through midadolescence: Enduring or transient effects? / John D. HALTIGAN in Development and Psychopathology, 25-1 (February 2013)
PermalinkThe Predictive Value of Microcephaly During the First Year of Life for Mental Retardation at Seven Years / H. DOLK in Developmental Medicine & Child Neurology, 33-11 (November 1991)
PermalinkThe Predictive Value of the AQ and the SRS-A in the Diagnosis of ASD in Adults in Clinical Practice / M. L. BEZEMER in Journal of Autism and Developmental Disorders, 51-7 (July 2021)
PermalinkThe predictors of change in reflective parenting therapy: Uncovering the influence of parental reflective functioning and child temperament in predicting the improvement in parent-child relationship and child outcome following DUET group intervention / Naama ATZABA-PORIA in Development and Psychopathology, 35-4 (October 2023)
PermalinkThe presence of migraines and its association with sensory hyperreactivity and anxiety symptomatology in children with autism spectrum disorder / Jillian C SULLIVAN in Autism, 18-6 (August 2014)
PermalinkThe Prevalence and Associations of Psychiatric Disorder in Children in Kerala, South India / Richard HACKETT in Journal of Child Psychology and Psychiatry, 40-5 (July 1999)
PermalinkThe Prevalence and Correlates of Involvement in the Criminal Justice System Among Youth on the Autism Spectrum / Julianna RAVA in Journal of Autism and Developmental Disorders, 47-2 (February 2017)
PermalinkThe prevalence and developmental course of auditory processing differences in autistic children / Bonnie K. LAU in Autism Research, 16-7 (July 2023)
PermalinkThe prevalence and incidence of early-onset dementia among adults with autism spectrum disorder / G. VIVANTI in Autism Research, 14-10 (October 2021)
PermalinkThe Prevalence and Incidence of Mental Ill-Health in Adults with Autism and Intellectual Disabilities / Craig MELVILLE in Journal of Autism and Developmental Disorders, 38-9 (October 2008)
PermalinkThe Prevalence and Phenomenology of Repetitive Behavior in Genetic Syndromes / Joanna MOSS in Journal of Autism and Developmental Disorders, 39-4 (April 2009)
PermalinkThe prevalence and profile of autism in Sturge-Weber syndrome / Jenny SLONEEM in Journal of Autism and Developmental Disorders, 52-5 (May 2022)
PermalinkThe Prevalence and Psychopathological Correlates of Sibling Bullying in Children with and without Autism Spectrum Disorder / U. TOSEEB in Journal of Autism and Developmental Disorders, 48-7 (July 2018)
PermalinkThe Prevalence of ADHD, ODD, Depression, and Anxiety in a Community Sample of 4-Year-Olds / John V. LAVIGNE in Journal of Clinical Child & Adolescent Psychology, 38-3 (May 2009)
PermalinkThe Prevalence of Anxiety and Mood Problems among Children with Autism and Asperger Syndrome / Joseph A. KIM in Autism, 4-2 (June 2000)
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