Literature DB >> 17075359

COMT Val108/158Met gene variant, birth weight, and conduct disorder in children with ADHD.

Sarojini M Sengupta1, Natalie Grizenko1, Norbert Schmitz1, George Schwartz1, Leila Ben Amor1, Johanne Bellingham1, Rosherrie DE Guzman1, Anna Polotskaia1, Marina Ter Stepanian1, Geeta Thakur1, Ridha Joober2.   

Abstract

OBJECTIVE: In a recent study, Thapar and colleagues reported that COMT "gene variant and birth weight predict early-onset antisocial behavior in children" with attention-deficit/hyperactivity disorder. We have attempted to replicate these findings in a group of ADHD children using a similar research design.
METHOD: Children (n=191) between 6 and 12 years of age who were diagnosed with ADHD were included in the study. Conduct disorder was diagnosed according to DSM-IV criteria based on clinical evaluation and a structured interview (Diagnostic Interview Schedule for Children-IV). The mother's report on the child's birth weight was used in the analysis. Logistic regression analysis, with genotype and birth weight as independent variables and DSM-IV conduct disorder as the dependent variable, was conducted.
RESULTS: No significant main effects of genotype and birth weight or interaction effects on conduct disorder were observed.
CONCLUSION: In this sample of children diagnosed with ADHD, we find no association between the COMT ValMet gene variant, birth weight, and conduct disorder. Further investigations are required before using birth weight and COMT genotype as predictors of conduct disorder in children with attention-deficit/hyperactivity disorder, especially given the societal and legal ramifications of conduct disorder.

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Year:  2006        PMID: 17075359     DOI: 10.1097/01.chi.0000251212.44491.46

Source DB:  PubMed          Journal:  J Am Acad Child Adolesc Psychiatry        ISSN: 0890-8567            Impact factor:   8.829


  16 in total

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3.  Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes.

Authors:  Patricia A Brennan; Constance Hammen; Patrick Sylvers; William Bor; Jake Najman; Penelope Lind; Grant Montgomery; Alicia K Smith
Journal:  Biol Psychol       Date:  2011-02-26       Impact factor: 3.251

4.  Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.

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5.  The association between the catechol-O-methyltransferase Val108/158Met polymorphism and hyperactive-impulsive and inattentive symptoms in youth.

Authors:  Matea Nikolac Perkovic; Evelyn Kiive; Gordana Nedic Erjavec; Toomas Veidebaum; Mario Curkovic; Katarina Dodig-Curkovic; Dorotea Muck-Seler; Jaanus Harro; Nela Pivac
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6.  Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant.

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7.  COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10-14.

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Review 8.  ADHD genetics: 2007 update.

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9.  A Meta-Analysis of the Association Between Birth Weight and Attention Deficit Hyperactivity Disorder.

Authors:  Allison M Momany; Jaclyn M Kamradt; Molly A Nikolas
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Review 10.  Research review: DSM-V conduct disorder: research needs for an evidence base.

Authors:  Terrie E Moffitt; Louise Arseneault; Sara R Jaffee; Julia Kim-Cohen; Karestan C Koenen; Candice L Odgers; Wendy S Slutske; Essi Viding
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