Abstract
Attention deficit hyperactivity disorder (ADHD) is a developmental syndrome expressed along three domains: inattention, hyperactive-impulsive, and combined type. Several investigations have recently examined the role of the dopamine 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 case 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. However, in the current study we fail to observe preferential transmission of the DRD4 exon III long 7 repeat allele, χ2 = 0.142, P < 0.1, df = 1. Nor was any preferential transmission observed when genotypes were compared, χ2 = 0.180, P > 0.1, df = 1. Possible reasons are discussed, especially lack of sufficient power in analying more refined phenotypes, why the current 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. (C) 2000 Wiley-Liss, Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 258-261 |
| Number of pages | 4 |
| Journal | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics |
| Volume | 96 |
| Issue number | 3 |
| DOIs | |
| State | Published - 12 Jun 2000 |
| Externally published | Yes |
Keywords
- Association
- Attention deficit hyperactivity disorder (ADHD)
- Complex genetic disease
- Dopamine D4 receptor exon III
- Haplotype relative risk
- Impulsive
- Polymorphism
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