5-HTTLPR polymorphism influences prefrontal neurochemical metabolites in autism spectrum disorder

Psychiatry Res. 2010 Aug 30;183(2):170-3. doi: 10.1016/j.pscychresns.2010.04.015. Epub 2010 Jul 8.

Abstract

We investigated whether the promoter region of the serotonin transporter gene (5-HTTLPR) polymorphism influenced neurochemical metabolism in 26 individuals with autism spectrum disorder. Individuals with the S/S genotype of the 5-HTTLPR polymorphism showed significantly lower levels of N-acetylaspartate/creatine in the right medial prefrontal cortex compared with those with the S/L genotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Analysis of Variance
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / metabolism
  • Child
  • Child Development Disorders, Pervasive / genetics*
  • Child Development Disorders, Pervasive / pathology*
  • Creatine / metabolism
  • Female
  • Humans
  • Magnetic Resonance Spectroscopy / methods
  • Male
  • Neurochemistry*
  • Polymorphism, Genetic / genetics*
  • Prefrontal Cortex / metabolism*
  • Protons
  • Serotonin Plasma Membrane Transport Proteins / genetics*

Substances

  • Protons
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins
  • Aspartic Acid
  • N-acetylaspartate
  • Creatine