TY - JOUR
T1 - High loading of polygenic risk for ADHD in children with comorbid aggression
AU - Hamshere, Marian L
AU - Langley, Kate
AU - Martin, Joanna
AU - Agha, Sharifah Shameem
AU - Stergiakouli, Evangelia
AU - Anney, Richard J L
AU - Buitelaar, Jan
AU - Faraone, Stephen V
AU - Lesch, Klaus-Peter
AU - Neale, Benjamin M
AU - Franke, Barbara
AU - Sonuga-Barke, Edmund
AU - Asherson, Philip
AU - Merwood, Andrew
AU - Kuntsi, Jonna
AU - Medland, Sarah E
AU - Ripke, Stephan
AU - Steinhausen, Hans-Christoph
AU - Freitag, Christine
AU - Reif, Andreas
AU - Renner, Tobias J
AU - Romanos, Marcel
AU - Romanos, Jasmin
AU - Warnke, Andreas
AU - Meyer, Jobst
AU - Palmason, Haukur
AU - Vasquez, Alejandro Arias
AU - Lambregts-Rommelse, Nanda
AU - Roeyers, Herbert
AU - Biederman, Joseph
AU - Doyle, Alysa E
AU - Hakonarson, Hakon
AU - Rothenberger, Aribert
AU - Banaschewski, Tobias
AU - Oades, Robert D
AU - McGough, James J
AU - Kent, Lindsey
AU - Williams, Nigel
AU - Owen, Michael J
AU - Holmans, Peter
AU - O'Donovan, Michael C
AU - Thapar, Anita
PY - 2013/8
Y1 - 2013/8
N2 - OBJECTIVE Although attention deficit hyperactivity disorder (ADHD) is highly heritable, genome-wide association studies (GWAS) have not yet identified any common genetic variants that contribute to risk. There is evidence that aggression or conduct disorder in children with ADHD indexes higher genetic loading and clinical severity. The authors examine whether common genetic variants considered en masse as polygenic scores for ADHD are especially enriched in children with comorbid conduct disorder. METHOD Polygenic scores derived from an ADHD GWAS meta-analysis were calculated in an independent ADHD sample (452 case subjects, 5,081 comparison subjects). Multivariate logistic regression analyses were employed to compare polygenic scores in the ADHD and comparison groups and test for higher scores in ADHD case subjects with comorbid conduct disorder relative to comparison subjects and relative to those without comorbid conduct disorder. Association with symptom scores was tested using linear regression. RESULTS Polygenic risk for ADHD, derived from the meta-analysis, was higher in the independent ADHD group than in the comparison group. Polygenic score was significantly higher in ADHD case subjects with conduct disorder relative to ADHD case subjects without conduct disorder. ADHD polygenic score showed significant association with comorbid conduct disorder symptoms. This relationship was explained by the aggression items. CONCLUSIONS Common genetic variation is relevant to ADHD, especially in individuals with comorbid aggression. The findings suggest that the previously published ADHD GWAS meta-analysis contains weak but true associations with common variants, support for which falls below genome-wide significance levels. The findings also highlight the fact that aggression in ADHD indexes genetic as well as clinical severity.
AB - OBJECTIVE Although attention deficit hyperactivity disorder (ADHD) is highly heritable, genome-wide association studies (GWAS) have not yet identified any common genetic variants that contribute to risk. There is evidence that aggression or conduct disorder in children with ADHD indexes higher genetic loading and clinical severity. The authors examine whether common genetic variants considered en masse as polygenic scores for ADHD are especially enriched in children with comorbid conduct disorder. METHOD Polygenic scores derived from an ADHD GWAS meta-analysis were calculated in an independent ADHD sample (452 case subjects, 5,081 comparison subjects). Multivariate logistic regression analyses were employed to compare polygenic scores in the ADHD and comparison groups and test for higher scores in ADHD case subjects with comorbid conduct disorder relative to comparison subjects and relative to those without comorbid conduct disorder. Association with symptom scores was tested using linear regression. RESULTS Polygenic risk for ADHD, derived from the meta-analysis, was higher in the independent ADHD group than in the comparison group. Polygenic score was significantly higher in ADHD case subjects with conduct disorder relative to ADHD case subjects without conduct disorder. ADHD polygenic score showed significant association with comorbid conduct disorder symptoms. This relationship was explained by the aggression items. CONCLUSIONS Common genetic variation is relevant to ADHD, especially in individuals with comorbid aggression. The findings suggest that the previously published ADHD GWAS meta-analysis contains weak but true associations with common variants, support for which falls below genome-wide significance levels. The findings also highlight the fact that aggression in ADHD indexes genetic as well as clinical severity.
KW - Aggression
KW - Anxiety Disorders
KW - Attention Deficit Disorder with Hyperactivity
KW - Child
KW - Child, Preschool
KW - Comorbidity
KW - Conduct Disorder
KW - Depressive Disorder
KW - Female
KW - Genetic Predisposition to Disease
KW - Genetic Variation
KW - Great Britain
KW - Humans
KW - Male
KW - Multifactorial Inheritance
U2 - 10.1176/appi.ajp.2013.12081129
DO - 10.1176/appi.ajp.2013.12081129
M3 - Article (Academic Journal)
C2 - 23599091
SN - 0002-953X
VL - 170
SP - 909
EP - 916
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 8
ER -