Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes

Naomi Lowe, Aiveen Kirley, Ziarih Hawi, Pak Sham, Harvey Wickham, Christopher J. Kratochvil, Shelley D. Smith, Saretta Y. Lee, Florence Levy, Lindsey Kent, Fiona Middle, Luis A. Rohde, Tatiana Roman, Eda Tahir, Yanke Yazgan, Philip Asherson, Jonathan Mil, Anita Thapar, Antony Payton, Richard D. ToddTimothy Stephens, Richard P. Ebstein, Iris Manor, Cathy L. Barr, Karen G. Wigg, Richard J. Sinke, Jan K. Buitelaar, Susan L. Smalley, Stan F. Nelson, Joseph Biederman, Stephen V. Faraone, Michael Gill

Research output: Contribution to journalArticle

159 Scopus citations

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a highly heritable, heterogeneous disorder of early onset, consisting of a triad of symptoms: inattention, hyperactivity, and impulsivity. The disorder has a significant genetic component, and theories of etiology include abnormalities in the dopaminergic system, with DRD4, DAT1, SNAP25, and DRD5 being implicated as major susceptibility genes. An initial report of association between ADHD and the common 148-bp allele of a microsatellite marker located 18.5 kb from the DRD5 gene has been followed by several studies showing nonsignificant trends toward association with the same allele. To establish the postulated association of the (CA)n repeat with ADHD, we collected genotypic information from 14 independent samples of probands and their parents, analyzed them individually and, in the absence of heterogeneity, analyzed them as a joint sample. The joint analysis showed association with the DRD5 locus (P = .00005; odds ratio 1.24; 95% confidence interval 1.12-1.38). This association appears to be confined to the predominantly inattentive and combined clinical subtypes.

Original languageEnglish (US)
Pages (from-to)348-356
Number of pages9
JournalAmerican Journal of Human Genetics
Volume74
Issue number2
DOIs
StatePublished - Feb 2004

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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