The DRD2 Taql polymorphism and symptoms of attention deficit hyperactivity disorder

D. C. Rowe, E. J.C.G. Van Den Oord, C. Stever, L. N. Giedinghagen, J. M.C. Gard, Hobart H. Cleveland, III, M. Gilson, S. T. Terris, J. H. Mohr, S. Sherman, A. Abramowitz, I. D. Waldman

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Abstract

The relationship of the DRD2 Taql-A1 hyperactive/impulsive and inattentive attention deficit hyperactivity disorder (ADHD) in children and adolescents was examined in a sample of clinic-referred children and their siblings, and control children and their siblings (n = 236). The contribution of genetic dominance and additivity to mean differences among the A2A2, A1A2, and A1A1 genotypes was estimated using structural equation modeling. The effect of genetic additivity was statistically significant for both traits in an analysis of all children. The heritability from the DRD2 locus was estimated at 4.27% for hyperactive-impulsive symptoms and 2.12% for inattentive symptoms. Children with the A2A2 genotype had the highest mean level of symptoms. To control for any possible effects of population stratification, this analysis was repeated with parental genotypes as controls. In this smaller sample, although the direction of the effect was the same as that in the whole sample, the genotypic differences failed to reach conventional significance levels and the effect sizes were smaller (h2 =1.62% and 0.79%, respectively). Furthermore, a genotype relative risk test of children who had questionnaire-based diagnoses of ADHD also failed to yield evidence of either association or linkage. Given that the A1 allele was expected to be the high risk allele, and that results were non-significant in tests that controlled for population heterogeneity, we doubt that this DRD2 polymorphism influences symptoms of ADHD in childhood.

Original languageEnglish (US)
Pages (from-to)580-586
Number of pages7
JournalMolecular Psychiatry
Volume4
Issue number6
DOIs
StatePublished - Jan 1 1999

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Attention Deficit Disorder with Hyperactivity
Genotype
Siblings
Alleles
Population Characteristics
Population

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience

Cite this

Rowe, D. C., Van Den Oord, E. J. C. G., Stever, C., Giedinghagen, L. N., Gard, J. M. C., Cleveland, III, H. H., ... Waldman, I. D. (1999). The DRD2 Taql polymorphism and symptoms of attention deficit hyperactivity disorder. Molecular Psychiatry, 4(6), 580-586. https://doi.org/10.1038/sj.mp.4000567
Rowe, D. C. ; Van Den Oord, E. J.C.G. ; Stever, C. ; Giedinghagen, L. N. ; Gard, J. M.C. ; Cleveland, III, Hobart H. ; Gilson, M. ; Terris, S. T. ; Mohr, J. H. ; Sherman, S. ; Abramowitz, A. ; Waldman, I. D. / The DRD2 Taql polymorphism and symptoms of attention deficit hyperactivity disorder. In: Molecular Psychiatry. 1999 ; Vol. 4, No. 6. pp. 580-586.
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Rowe, DC, Van Den Oord, EJCG, Stever, C, Giedinghagen, LN, Gard, JMC, Cleveland, III, HH, Gilson, M, Terris, ST, Mohr, JH, Sherman, S, Abramowitz, A & Waldman, ID 1999, 'The DRD2 Taql polymorphism and symptoms of attention deficit hyperactivity disorder', Molecular Psychiatry, vol. 4, no. 6, pp. 580-586. https://doi.org/10.1038/sj.mp.4000567

The DRD2 Taql polymorphism and symptoms of attention deficit hyperactivity disorder. / Rowe, D. C.; Van Den Oord, E. J.C.G.; Stever, C.; Giedinghagen, L. N.; Gard, J. M.C.; Cleveland, III, Hobart H.; Gilson, M.; Terris, S. T.; Mohr, J. H.; Sherman, S.; Abramowitz, A.; Waldman, I. D.

In: Molecular Psychiatry, Vol. 4, No. 6, 01.01.1999, p. 580-586.

Research output: Contribution to journalArticle

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T1 - The DRD2 Taql polymorphism and symptoms of attention deficit hyperactivity disorder

AU - Rowe, D. C.

AU - Van Den Oord, E. J.C.G.

AU - Stever, C.

AU - Giedinghagen, L. N.

AU - Gard, J. M.C.

AU - Cleveland, III, Hobart H.

AU - Gilson, M.

AU - Terris, S. T.

AU - Mohr, J. H.

AU - Sherman, S.

AU - Abramowitz, A.

AU - Waldman, I. D.

PY - 1999/1/1

Y1 - 1999/1/1

N2 - The relationship of the DRD2 Taql-A1 hyperactive/impulsive and inattentive attention deficit hyperactivity disorder (ADHD) in children and adolescents was examined in a sample of clinic-referred children and their siblings, and control children and their siblings (n = 236). The contribution of genetic dominance and additivity to mean differences among the A2A2, A1A2, and A1A1 genotypes was estimated using structural equation modeling. The effect of genetic additivity was statistically significant for both traits in an analysis of all children. The heritability from the DRD2 locus was estimated at 4.27% for hyperactive-impulsive symptoms and 2.12% for inattentive symptoms. Children with the A2A2 genotype had the highest mean level of symptoms. To control for any possible effects of population stratification, this analysis was repeated with parental genotypes as controls. In this smaller sample, although the direction of the effect was the same as that in the whole sample, the genotypic differences failed to reach conventional significance levels and the effect sizes were smaller (h2 =1.62% and 0.79%, respectively). Furthermore, a genotype relative risk test of children who had questionnaire-based diagnoses of ADHD also failed to yield evidence of either association or linkage. Given that the A1 allele was expected to be the high risk allele, and that results were non-significant in tests that controlled for population heterogeneity, we doubt that this DRD2 polymorphism influences symptoms of ADHD in childhood.

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