A Common Polymorphism in SCN2A Predicts General Cognitive Ability through Effects on PFC Physiology

J Cogn Neurosci. 2015 Sep;27(9):1766-74. doi: 10.1162/jocn_a_00826. Epub 2015 May 11.

Abstract

Here we provide novel convergent evidence across three independent cohorts of healthy adults (n = 531), demonstrating that a common polymorphism in the gene encoding the α2 subunit of neuronal voltage-gated type II sodium channels (SCN2A) predicts human general cognitive ability or "g." Using meta-analysis, we demonstrate that the minor T allele of a common polymorphism (rs10174400) in SCN2A is associated with significantly higher "g" independent of gender and age. We further demonstrate using resting-state fMRI data from our discovery cohort (n = 236) that this genetic advantage may be mediated by increased capacity for information processing between the dorsolateral PFC and dorsal ACC, which support higher cognitive functions. Collectively, these findings fill a gap in our understanding of the genetics of general cognitive ability and highlight a specific neural mechanism through which a common polymorphism shapes interindividual variation in "g."

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Brain / physiology*
  • Brain Mapping
  • Cognition / physiology*
  • Cohort Studies
  • Female
  • Genotyping Techniques
  • Humans
  • Individuality
  • Magnetic Resonance Imaging
  • Male
  • NAV1.2 Voltage-Gated Sodium Channel / genetics*
  • Neural Pathways / physiology
  • Neuropsychological Tests
  • Polymorphism, Genetic*
  • Rest
  • Young Adult

Substances

  • NAV1.2 Voltage-Gated Sodium Channel
  • SCN2A protein, human