No association between Cholinergic Muscarinic Receptor 2 (CHRM2) genetic variation and cognitive abilities in three independent samples

Behav Genet. 2009 Sep;39(5):513-23. doi: 10.1007/s10519-009-9274-z. Epub 2009 May 6.

Abstract

Cognitive ability has a substantial genetic component and more than 15 candidate genes have been identified over the past 8 years. One gene that has been associated with general cognitive ability is the cholinergic muscarinic 2 receptor (CHRM2). In an attempt to replicate this finding we typed marker rs8191992 (the originally reported CHRM2 SNP) in two population based cohorts-one Scottish aged over 50 years (N = 2,091) and the other English comprising non-demented elderly participants (N = 758)-and a family-based Australian adolescent sample (N = 1,537). An additional 29 SNPs in CHRM2 were typed in the Australian sample and a further seven in the English cohort. No significant association was found between CHRM2 and diverse measures of cognitive ability in any of the samples. In conclusion, this study does not support a role for CHRM2 in cognitive ability.

Publication types

  • Research Support, Non-U.S. Gov't
  • Twin Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Australia
  • Cognition / physiology*
  • Cohort Studies
  • England
  • Family Health
  • Female
  • Genetic Markers
  • Genetic Variation*
  • Humans
  • Intelligence / genetics
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Receptor, Muscarinic M2 / genetics*
  • Scotland

Substances

  • CHRM2 protein, human
  • Genetic Markers
  • Receptor, Muscarinic M2