Cited by 100Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on BehaviorGenetic Associations and Epidemiology

Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: A preliminary study

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Biederman, Joseph, Kim, Jang Woo, Doyle, Alysa E., Mick, Eric, Fagerness, Jesen, Smoller, Jordan W., Faraone, Stephen V.·2008·American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Abstract

A growing body of literature finds gender differences in ADHD. However, little is known about the causes of these differences. One possibility is that ADHD risk genes have sexually dimorphic effects. We have investigated four ADHD candidate genes (COMT, SLC6A2, MAOA, SLC6A4) for which there is evidence of sexually dimorphic effects. Past neurobiological and genetic studies suggest that COMT, and SLC6A4 variants may have a greater influence on males and that SLC6A2, and MAOA variants may have a greater influence on females. Our results indicate that genetic associations are stronger when stratified by sex and in the same direction as the previous neurobiological studies indicate: associations were stronger in males for COMT, SLC6A4 and stronger in females for SLC6A2, MAOA. Moreover, we found a statistically significant gender effect in the case of COMT (P = 0.007) when we pooled our work with a prior study. In conclusion, we have found some evidence suggesting that the genetic association for these genes with ADHD may be influenced by the sex of the affected individual. Although our results are not fully validated yet, they should motivate further investigation of gender effects in ADHD genetic association studies. © 2008 Wiley‐Liss, Inc.

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References 67 · Cited by 100

Research works printed but not linked: 3

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Authors
Biederman, J., Kim, J. W., Doyle, A. E., Mick, E., Fagerness, J., Smoller, J. W., & Faraone, S. V.
Affiliations
  • Harvard University (US)
  • SUNY Upstate Medical University (US)
Corresponding author
Biederman, Joseph
Venue
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Publisher
Wiley
Published
2008-10-20
Volume
147B
Issue
8
Pages
1511-1518
ISSN
  • 1552-4841 (ISSN-L)
  • 1552-485X
OpenAlex
W2099784662
Cited by
100
References
67
Citations by year
2026: 1 · 2025: 1 · 2024: 1 · 2023: 4 · 2022: 2 · 2021: 3 · 2020: 1 · 2019: 2 · 2018: 4 · 2017: 8 · 2016: 7 · 2015: 12 · 2014: 8 · 2013: 7 · 2012: 9
FWCI
7.03
Type
journal article
Language
en
Open access
Locations
  • American Journal of Medical Genetics Part B Neuropsychiatric Genetics (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Alliance for Research on Schizophrenia and Depression
  • National Institutes of Health
  • National Institute of Mental Health (R01MH066877, R01MH66877)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD37999, R01HD37694, R01HD037694, R01HD037999)
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, sex differences, catechol-O-methyltransferase, norepinephrine transporter, monoamine oxidase A, serotonin transporter, genetic association, candidate genes, sex-stratified analysis
MeSH terms
Adolescent, Adult, Alleles, Attention Deficit Disorder with Hyperactivity, Catechol O-Methyltransferase, Child, Child, Preschool, Female, Genetic Markers, Genotype, Humans, Interviews as Topic, Male, Monoamine Oxidase, Sex Factors, Linkage Disequilibrium, Chi-Square Distribution, Case-Control Studies, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Siblings, Dopamine Plasma Membrane Transport Proteins, Serotonin Plasma Membrane Transport Proteins, Young Adult

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