Further evidence for the association between attention-deficit/hyperactivity disorder and the dopamine-beta-hydroxylase gene

Am J Med Genet. 2002 Mar 8;114(2):154-8. doi: 10.1002/ajmg.10194.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a very common and heterogeneous psychiatric disorder of childhood with marked inattentive, hyperactive, and impulsive symptoms. The DBH gene, the locus that encodes the enzyme dopamine-beta-hydroxylase (DbetaH), seems to be an important candidate gene for association studies, since DbetaH catalyzes the conversion of dopamine to norepinephrine. The aim of this study was to test for association between the DBH gene and ADHD in a sample of 88 Brazilian nuclear families. Haplotype relative risk (HRR) analysis of the DBH TaqI restriction site polymorphism showed a preferential transmission of the TaqI A2 allele in our whole ADHD sample (chi(2)=3.61, one-tailed P=0.03). The significant effect of the A2 allele was stronger when only families with no ADHD parental diagnosis were considered (chi(2)=5.42, one-tailed P=0.01). Our results suggest a contribution of this gene to ADHD susceptibility, partially replicating previous findings that have demonstrated an association between the DBH TaqI A2 allele and ADHD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Attention Deficit Disorder with Hyperactivity / enzymology
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • DNA / genetics
  • DNA / metabolism
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Dopamine beta-Hydroxylase / genetics*
  • Family Health
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Male
  • Nuclear Family
  • Polymorphism, Genetic

Substances

  • DNA
  • Dopamine beta-Hydroxylase
  • Deoxyribonucleases, Type II Site-Specific
  • TCGA-specific type II deoxyribonucleases