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SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families
Author(s) -
Kollins S.H.,
Anastopoulos A.D.,
Lachiewicz A.M.,
FitzGerald D.,
MorrisseyKane E.,
Garrett M.E.,
Keatts S.L.,
AshleyKoch A.E.
Publication year - 2008
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.30876
Subject(s) - single nucleotide polymorphism , candidate gene , haplotype , snp , endophenotype , genetics , biology , gene , proband , monoaminergic , phenotype , genetic association , norepinephrine transporter , genotype , neuroscience , receptor , transporter , mutation , cognition , serotonin
Haplotype‐tagging SNP analyses were conducted to identify molecular genetic substrates of quantitative phenotypes derived from performance on a Continuous Performance Task (CPT). Three hundred sixty‐four individuals were sampled from 152 families ascertained on the basis of at least one child having ADHD. Probands, their affected and unaffected siblings, and parents were administered a CPT. Four different components of performance were analyzed and tested for association with SNPs from 10 candidate genes involved in monoaminergic function. After correcting for multiple comparisons and controlling for multiple individuals from the same family, significant associations were identified between commission errors and SNPs in the DRD2 gene (rs2075654, rs1079596), and between reaction time variability and a SNP in the NET gene (rs3785155). These findings suggest that commission errors and reaction time variability are excellent candidates as ADHD endophenotypes based on previously published criteria. Results also shed light on the molecular genetic basis of specific processes that may underlie the disorder. © 2008 Wiley‐Liss, Inc.