Phenotype studies of the DRD4 gene Polymorphisms in ADHD:: Association with oppositional defiant disorder and positive family history

被引:52
作者
Kirley, A
Lowe, N
Mullins, C
McCarron, M
Daly, G
Waldman, I
Fitzgerald, M
Gill, M
Hawi, Z [1 ]
机构
[1] Univ Dublin Trinity Coll, Dept Genet, Dublin 2, Ireland
[2] Univ Dublin Trinity Coll, Dept Psychiat, Dublin 2, Ireland
[3] Emory Univ, Dept Psychol, Atlanta, GA 30322 USA
关键词
DRD4; polymorphisms; ADHD; ODD; transmission disequilibrium test (TDT); endophenotype;
D O I
10.1002/ajmg.b.30072
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 (chi(2)=6.74, df=1, P=0.01, OR=2.45) The DRD4 7-repeat allele was also significantly associated with family history positive ADHD (chi(2)=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. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:38 / 42
页数:5
相关论文
共 34 条
[1]  
ANGOLD A, 1995, PSYCHOL MED, V25, P739, DOI 10.1017/S003329170003498X
[2]   THE ADOLESCENT OUTCOME OF HYPERACTIVE-CHILDREN DIAGNOSED BY RESEARCH CRITERIA .3. MOTHER-CHILD INTERACTIONS, FAMILY CONFLICTS AND MATERNAL PSYCHOPATHOLOGY [J].
BARKLEY, RA ;
FISCHER, M ;
EDELBROCK, C ;
SMALLISH, L .
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES, 1991, 32 (02) :233-255
[3]  
BIEDERMAN J, 1995, ARCH GEN PSYCHIAT, V52, P464
[4]   CONVERGENCE OF THE CHILD-BEHAVIOR CHECKLIST WITH STRUCTURED INTERVIEW-BASED PSYCHIATRIC DIAGNOSES OF ADHD CHILDREN WITH AND WITHOUT COMORBIDITY [J].
BIEDERMAN, J ;
FARAONE, SV ;
DOYLE, A ;
LEHMAN, BK ;
KRAUS, I ;
PERRIN, J ;
TSUANG, MT .
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES, 1993, 34 (07) :1241-1251
[5]  
BIRD HR, 1997, J AM ACAD CHILD ADOL, V26, P207
[6]   DIAGNOSTIC-ACCURACY OF THE CHILD-BEHAVIOR CHECKLIST SCALES FOR ATTENTION-DEFICIT HYPERACTIVITY DISORDER - A RECEIVER-OPERATING CHARACTERISTIC ANALYSIS [J].
CHEN, WJ ;
FARAONE, SV ;
BIEDERMAN, J ;
TSUANG, MT .
JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1994, 62 (05) :1017-1025
[7]   QTL association analysis of the DRD4 exon 3 VNTR polymorphism in a population sample of children screened with a parent rating scale for ADHD symptoms [J].
Curran, S ;
Mill, J ;
Sham, P ;
Rijsdijk, F ;
Marusic, K ;
Taylor, E ;
Asherson, P .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (04) :387-393
[8]   BEHAVIORAL RATINGS OF CHILDREN DIAGNOSED FOR ATTENTION-DEFICIT DISORDER [J].
EDELBROCK, C .
PSYCHIATRIC ANNALS, 1986, 16 (01) :36-40
[9]   Genetics of childhood disorders: XX. ADHD, part 4: Is ADHD genetically heterogeneous? [J].
Faraone, SV .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2000, 39 (11) :1455-1457
[10]   Meta-analysis of the association between the 7-repeat allele of the dopamine D4 receptor gene and attention deficit hyperactivity disorder [J].
Faraone, SV ;
Doyle, AE ;
Mick, E ;
Biederman, J .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (07) :1052-1057