TY - JOUR
T1 - Phenotype studies of the DRD4 gene polymorphisms in ADHD
T2 - Association with oppositional defiant disorder and positive family history
AU - Kirley, Aiveen
AU - Lowe, Naomi
AU - Mullins, Céline
AU - McCarron, Mary
AU - Daly, Grainne
AU - Waldman, Irwin
AU - Fitzgerald, Michael
AU - Gill, Michael
AU - Hawi, Ziarih
PY - 2004/11/15
Y1 - 2004/11/15
N2 - The objective of this study was to investigate association of DRD4 polymorphisms with ADHD subtypes for which there is evidence for increased heritability. The genetic variants tested were the 120 bp insertion/deletion, the -616, -521, -376, and the 48 bp DRD4 VNTR. The primary analyses were of association with oppositional defiant disorder (ODD), conduct disorder (CD), and diagnostic subtypes. Secondary analyses of clinical subtype were exploratory in nature and included analysis of association of DRD4 polymorphisms with family history of ADHD. We observed significant association between DRD4 7-repeat allele transmission and ADHD children with comorbid ODD (χ2 = 6.74, df = 1, P = 0-01, OR = 2.45) The DRD4 7-repeat allele was also significantly associated with family history positive ADHD (χ2 =10.12, df = 1, P = 0.0021, OR = 3.57). We observed no significant distortion in the transmission of any of the tested DRD4 variants with inattentive or hyperactive-impulsive subtypes or symptom dimensions. In conclusion, our findings of increased DRD4 7-repeat allele transmission in ODD extend those reported by Holmes et al. [2002: Am J Med Genet Neuropsychiatr 114:150-153]. To our knowledge, this is the first study to report association of the DRD4 7-repeat allele with ADHD children who have a positive family history of ADHD. Overall, the results from this study support the investigation of clinical subtypes in molecular genetic studies of ADHD.
AB - The objective of this study was to investigate association of DRD4 polymorphisms with ADHD subtypes for which there is evidence for increased heritability. The genetic variants tested were the 120 bp insertion/deletion, the -616, -521, -376, and the 48 bp DRD4 VNTR. The primary analyses were of association with oppositional defiant disorder (ODD), conduct disorder (CD), and diagnostic subtypes. Secondary analyses of clinical subtype were exploratory in nature and included analysis of association of DRD4 polymorphisms with family history of ADHD. We observed significant association between DRD4 7-repeat allele transmission and ADHD children with comorbid ODD (χ2 = 6.74, df = 1, P = 0-01, OR = 2.45) The DRD4 7-repeat allele was also significantly associated with family history positive ADHD (χ2 =10.12, df = 1, P = 0.0021, OR = 3.57). We observed no significant distortion in the transmission of any of the tested DRD4 variants with inattentive or hyperactive-impulsive subtypes or symptom dimensions. In conclusion, our findings of increased DRD4 7-repeat allele transmission in ODD extend those reported by Holmes et al. [2002: Am J Med Genet Neuropsychiatr 114:150-153]. To our knowledge, this is the first study to report association of the DRD4 7-repeat allele with ADHD children who have a positive family history of ADHD. Overall, the results from this study support the investigation of clinical subtypes in molecular genetic studies of ADHD.
KW - ADHD
KW - DRD4 polymorphisms
KW - Endophenotype
KW - ODD
KW - Transmission disequilibrium test (TDT)
UR - http://www.scopus.com/inward/record.url?scp=7644232651&partnerID=8YFLogxK
U2 - 10.1002/ajmg.b.30072
DO - 10.1002/ajmg.b.30072
M3 - Article
C2 - 15389763
AN - SCOPUS:7644232651
VL - 131 B
SP - 38
EP - 42
JO - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
JF - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
SN - 1552-4841
IS - 1
ER -