Cited by 153Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on BehaviorGenetic Associations and Epidemiology

Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis

Kent, L, Doerry, U, Hardy, E, Parmar, R, Gingell, K, Hawi, Z, Kirley, A, Lowe, N +3 more·2002·Molecular Psychiatry

Abstract

Reduced central serotonergic activity has been implicated in poor impulse regulation and aggressive behaviour in animals, adults and also young children.(1,2) Two recently published studies have implicated variation at a polymorphism in the promoter of the serotonin transporter (5HTT; hSERT) in influencing susceptibility to ADHD.(3,4) Consistent with these results we have also found a trend for the long allele of the promoter polymorphism to influence susceptibility to ADHD in a sample of 113 ADHD parent proband trios (65 transmissions vs 49 non-transmissions, chi(2) = 2.25, P = 0.13). A pooled analysis of our, and these published results demonstrated a significant over representation of the long allele of the promoter in ADHD probands compared to controls (chi(2) = 7.14, P = 0.008). We have also examined two other 5HTT polymorphisms (the VNTR in intron 2 and the 3' UTR SNP). TDT analysis demonstrated preferential transmission of the T allele of the 3' UTR SNP (chi(2) = 4.06, P = 0.04). In addition, ETDT analysis of haplotypes demonstrated significant preferential transmission of haplotypes containing the T allele of the 3' UTR SNP with the long allele of the promoter polymorphism (chi(2) = 13.18, 3 df, P = 0.004) and the 10 repeat of the VNTR (chi(2) = 8.77, 3 df, P = 0.03). This study provides further evidence for the possible involvement of the serotonin transporter in susceptibility to ADHD.

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References 27 · Cited by 153

Authors
Kent, L., Doerry, U., Hardy, E., Parmar, R., Gingell, K., Hawi, Z., Kirley, A., Lowe, N., Fitzgerald, M., Gill, M., & Craddock, N.
Affiliations
  • University of Birmingham (GB)
  • Birmingham Children's Hospital (GB)
  • Trinity College Dublin (IE)
Corresponding author
Kent, L
Venue
Molecular Psychiatry
Published
2002-09-01
Volume
7
Issue
8
Pages
908-912
ISSN
  • 1359-4184 (ISSN-L)
  • 1476-5578
OpenAlex
W2072476269
Cited by
153
References
27
Citations by year
2026: 1 · 2025: 1 · 2024: 3 · 2023: 3 · 2022: 2 · 2021: 2 · 2020: 3 · 2019: 1 · 2018: 3 · 2017: 1 · 2016: 6 · 2015: 6 · 2014: 1 · 2013: 4 · 2012: 4
FWCI
7.99
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
  • Arrow@dit (Dublin Institute of Technology) (submittedVersion)
  • ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
Funders
Wellcome Trust
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
Keywords
attention deficit hyperactivity disorder, serotonin transporter, promoter polymorphism, long allele, variable number tandem repeats, haplotype transmission, genetic susceptibility, transmission disequilibrium test, serotonergic system
MeSH terms
Adult, Attention Deficit Disorder with Hyperactivity, Carrier Proteins, Child, Gene Frequency, Haplotypes, Humans, Membrane Glycoproteins, Nerve Tissue Proteins, Promoter Regions, Genetic, Genetic Variation, Genetic Predisposition to Disease, Membrane Transport Proteins, Serotonin Plasma Membrane Transport Proteins

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