No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD

J Neural Transm (Vienna). 2007;114(4):523-6. doi: 10.1007/s00702-006-0616-1. Epub 2007 Jan 15.

Abstract

Attention deficit/hyperactivity disorder (ADHD) is a highly heritable common neurodevelopmental disorder with onset in childhood. A coding SNP (rs6265, Val66Met) of the brain-derived neurotrophic factor gene (BDNF) has recently been associated with ADHD. More specifically, paternal over-transmission of the common Val66 allele to affected children had been observed. We aimed to confirm these findings in a large, sufficiently powered, and well characterized German ADHD family sample. The Val66Met polymorphism of BDNF was genotyped in 294 families comprising one or more affected sibs (468 children). Contrary to previous reports, we did not observe over-transmission of the common Val66 allele, from either parent to affected children. We did not find support for an involvement of the Val66 allele of the Val66Met polymorphism of BDNF in the pathogenesis of ADHD in our sample.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Brain-Derived Neurotrophic Factor / genetics*
  • Child
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Pedigree
  • Polymorphism, Single Nucleotide*
  • Valine / genetics

Substances

  • Brain-Derived Neurotrophic Factor
  • Valine