A haplotype relative risk study of the dopamine D4 receptor (DRD4) Exon III repeat polymorphism and attention deficit hyperactivity disorder (ADHD)

Citation
J. Eisenberg et al., A haplotype relative risk study of the dopamine D4 receptor (DRD4) Exon III repeat polymorphism and attention deficit hyperactivity disorder (ADHD), AM J MED G, 96(3), 2000, pp. 258-261
Citations number
29
Categorie Soggetti
Molecular Biology & Genetics
Journal title
AMERICAN JOURNAL OF MEDICAL GENETICS
ISSN journal
01487299 → ACNP
Volume
96
Issue
3
Year of publication
2000
Pages
258 - 261
Database
ISI
SICI code
0148-7299(20000612)96:3<258:AHRRSO>2.0.ZU;2-P
Abstract
Attention deficit hyperactivity disorder (ADHD) is a developmental syndrome expressed along three domains: inattention, hyperactive-impulsive, and com bined type. Several investigations have recently examined the role of the d opamine DRD4 exon III repeat polymorphism in ADHD. The long 7 repeat allele of this receptor was shown in three family-based studies, but not in one c ase control design, to be a risk factor for this disorder. We now report an additional family-based study of DRD4 exon III repeat region and ADHD, How ever, in the current study we fail to observe preferential transmission of the DRD4 exon III long 7 repeat allele, chi(2) = 0.142, P < 0.1 df = 1. Nor was any preferential transmission observed when genotypes were compared, c hi(2) = 0.180, P > 0.1, df = 1, Possible reasons are discussed, especially lack of sufficient power in analying more refined phenotypes, why the curre nt results in contrast to previous findings fail to support a role for the long form of the DRD4 receptor as a putative risk factor for ADHD. Am. J, M ed, Genet. (Neuropsychiatr, Genet.) 96:258-261, 2000, (C) 2000 Wiley-Liss, Inc.