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PMID: 11409696 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Association of DRD4 with attention problems in normal childhood development.

Psychiatric genetics ·Vol. 11 ·No. 1 ·2001-03-00 ·Pages 25-9

Schmidt LA, Fox NA, Perez-Edgar K, Hu S, Hamer DH

Abstract

Several previous studies found an association of clinically diagnosed attention deficit hyperactivity disorder with long alleles of a variation in the DRD4 dopamine receptor gene exon III coding sequence. We evaluated the DRD4 polymorphism in a non-clinically selected sample of children for whom maternal reports of attention problems were available at 4 and 7 years of age. There was a significant elevation in attention problem scores in children carrying DRD4 long alleles that accounted for 3-4% of total variation at each age and for 5-7% of the temporally stable component of the phenotype. Our results show that the DRD4 gene influences normal as well as pathological attention processes, and the results highlight the utility of longitudinal measurements in psychiatric genetics.

MeSH Terms
Attention Deficit Disorder with Hyperactivity/genetics Child Child Development/physiology Child, Preschool Exons Genetic Variation Humans Longitudinal Studies Phenotype Polymorphism, Genetic Receptors, Dopamine D2/genetics Receptors, Dopamine D4
Chemicals
DRD4 protein, human Receptors, Dopamine D2 Receptors, Dopamine D4
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schmidt L A
Department of Psychology, McMaster University, Hamilton, Ontario, Canada.
Fox N A
Perez-Edgar K
Hu S
Hamer D H
Article Info
Journal
Psychiatric genetics
Abbr.
Psychiatr Genet
ISSN
0955-8829
Published
2001-03-00
Pages
25-9
Language
English
Region
England
NLM ID
9106748
Subset
IM
Grants
NICHD NIH HHS · HD 17899 · United States
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