Please cite this article as follows: Lee J, Laurin N, Crosbie J, Ickowicz A, Pathare T, Malone M, Tannock R, Kennedy JL, Schachar R, Barr CL. 2006. Association Study of the Brain-Derived Neurotropic Factor (BDNF) Gene in Attention Deficit Hyperactivity Disorder. Am J Med Genet Part B 144B:976–981.
Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder†
Article first published online: 4 OCT 2007
Copyright © 2007 Wiley-Liss, Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Volume 144B, Issue 8, pages 976–981, 5 December 2007
How to Cite
Lee, J., Laurin, N., Crosbie, J., Ickowicz, A., Pathare, T., Malone, M., Tannock, R., Kennedy, J. L., Schachar, R. and Barr, C. L. (2007), Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder. Am. J. Med. Genet., 144B: 976–981. doi: 10.1002/ajmg.b.30437
- Issue published online: 13 NOV 2007
- Article first published online: 4 OCT 2007
- Manuscript Accepted: 16 AUG 2006
- Manuscript Received: 11 MAY 2006
- Hospital for Sick Children Psychiatric Endowment Fund
- Canadian Institutes of Health Research. Grant Numbers: MT14336, MOP14336
- attention deficit hyperactivity disorder (ADHD);
- brain-derived neurotropic factor;
- transmission/disequilibrium test
Attention deficit hyperactivity disorder (ADHD) is a prevalent neurodevelopmental childhood psychiatric disorder. Brain-derived neurotropic factor (BDNF) has been suggested to play a role in the pathogenesis of ADHD and two family-based association studies demonstrated an association of BDNF polymorphisms with ADHD. The aim of the current study was to investigate the BDNF gene for association with ADHD in a large sample of families from Toronto. The transmission of three polymorphisms of the BDNF gene (rs6265, rs11030104, and rs2049046) was examined in 266 nuclear families ascertained through a proband with ADHD (315 affected children) using the transmission/disequilibrium test (TDT). In addition, we conducted quantitative analysis to assess the relationship between these marker alleles and the symptom dimensions of ADHD (inattention and hyperactivity/impulsivity) and cognitive measures of working memory. None of the individual marker alleles showed significant evidence of association with ADHD, dimensional symptom scores, or working memory ability in our sample of ADHD families. There was no significant evidence for biased transmission of individual haplotypes with frequency >10% (global χ2 for these three haplotypes: χ2 = 6.349, df = 3, P = 0.096). One uncommon haplotype (A-G-G; frequency 2.2%) showed a significant association with ADHD in the categorical (χ2 = 5.293, df = 1, P = 0.021) and quantitative analyses (parents' rated inattention: Z = −2.504, P = 0.012; and hyperactivity/impulsivity: Z = −2.651, P = 0.008). These results should be interpreted cautiously, however, because of the low haplotype frequency. In light of the evidence for an involvement of BDNF in ADHD, further analysis of the BDNF gene in ADHD is warranted. © 2007 Wiley-Liss, Inc.