TY - JOUR
T1 - Conduct disorder and ADHD
T2 - evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
AU - Anney, Richard J L
AU - Lasky-Su, Jessica
AU - O'Dúshláine, Colm
AU - Kenny, Elaine
AU - Neale, Benjamin M
AU - Mulligan, Aisling
AU - Franke, Barbara
AU - Zhou, Kaixin
AU - Chen, Wai
AU - Christiansen, Hanna
AU - Arias-Vásquez, Alejandro
AU - Banaschewski, Tobias
AU - Buitelaar, Jan
AU - Ebstein, Richard
AU - Miranda, Ana
AU - Mulas, Fernando
AU - Oades, Robert D
AU - Roeyers, Herbert
AU - Rothenberger, Aribert
AU - Sergeant, Joseph
AU - Sonuga-Barke, Edmund
AU - Steinhausen, Hans
AU - Asherson, Philip
AU - Faraone, Stephen V
AU - Gill, Michael
N1 - Copyright 2008 Wiley-Liss, Inc.
PY - 2008/12/5
Y1 - 2008/12/5
N2 - Attention-deficit/hyperactivity disorder (ADHD) is typically characterized by inattention, excessive motor activity, impulsivity, and distractibility. Individuals with ADHD have significant impairment in family and peer relations, academic functioning, and show high co-morbidity with a wide range of psychiatric disorders including oppositional defiant disorder (ODD), conduct disorder (CD), anxiety disorder, depression, substance abuse, and pervasive developmental disorder (PDD). Family studies suggest that ADHD + CD represents a specific subtype of the ADHD disorder with familial risk factors only partly overlapping with those of ADHD alone. We performed a hypothesis-free analysis of the GAIN-ADHD sample to identify markers and genes important in the development of conduct problems in a European cohort of individuals with ADHD. Using the Family-Based Association Test (FBAT) package we examined three measures of conduct problems in 1,043,963 autosomal markers. This study is part of a series of exploratory analyses to identify candidate genes that may be important in ADHD and ADHD-related traits, such as conduct problems. We did not find genome-wide statistical significance (P < 5 x 10(-7)) for any of the tested markers and the three conduct problem traits. Fifty-four markers reached strong GWA signals (P < 10(-5)). We discuss these findings in the context of putative candidate genes and the implications of these findings in the understanding of the etiology of ADHD + CD. We aimed to achieve insight into the genetic etiology of a trait using a hypothesis-free study design and were able to identify a number of biologically interesting markers and genes for follow-up studies.
AB - Attention-deficit/hyperactivity disorder (ADHD) is typically characterized by inattention, excessive motor activity, impulsivity, and distractibility. Individuals with ADHD have significant impairment in family and peer relations, academic functioning, and show high co-morbidity with a wide range of psychiatric disorders including oppositional defiant disorder (ODD), conduct disorder (CD), anxiety disorder, depression, substance abuse, and pervasive developmental disorder (PDD). Family studies suggest that ADHD + CD represents a specific subtype of the ADHD disorder with familial risk factors only partly overlapping with those of ADHD alone. We performed a hypothesis-free analysis of the GAIN-ADHD sample to identify markers and genes important in the development of conduct problems in a European cohort of individuals with ADHD. Using the Family-Based Association Test (FBAT) package we examined three measures of conduct problems in 1,043,963 autosomal markers. This study is part of a series of exploratory analyses to identify candidate genes that may be important in ADHD and ADHD-related traits, such as conduct problems. We did not find genome-wide statistical significance (P < 5 x 10(-7)) for any of the tested markers and the three conduct problem traits. Fifty-four markers reached strong GWA signals (P < 10(-5)). We discuss these findings in the context of putative candidate genes and the implications of these findings in the understanding of the etiology of ADHD + CD. We aimed to achieve insight into the genetic etiology of a trait using a hypothesis-free study design and were able to identify a number of biologically interesting markers and genes for follow-up studies.
KW - Algorithms
KW - Antisocial Personality Disorder
KW - Attention Deficit Disorder with Hyperactivity
KW - Attention Deficit and Disruptive Behavior Disorders
KW - Child
KW - Child Behavior Disorders
KW - Cohort Studies
KW - Comorbidity
KW - Conduct Disorder
KW - Europe
KW - Genetic Markers
KW - Genome, Human
KW - Genome-Wide Association Study
KW - Humans
KW - Linkage Disequilibrium
KW - Oligonucleotide Array Sequence Analysis
KW - Pedigree
KW - Polymorphism, Single Nucleotide
KW - Psychiatric Status Rating Scales
KW - Quantitative Trait Loci
KW - Journal Article
KW - Multicenter Study
KW - Research Support, N.I.H., Extramural
U2 - 10.1002/ajmg.b.30871
DO - 10.1002/ajmg.b.30871
M3 - Article
C2 - 18951430
SN - 1552-4841
VL - 147B
SP - 1369
EP - 1378
JO - American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
JF - American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
IS - 8
ER -