Serotonin transporter genotype is associated with cognitive performance but not regional 5-HT1A receptor binding in humans

Int J Neuropsychopharmacol. 2009 Jul;12(6):783-92. doi: 10.1017/S1461145708009759. Epub 2009 Jan 6.

Abstract

The human serotonin transporter (5-HTT) gene is one of the most extensively studied in psychiatry. A functional polymorphism in the promoter region of the 5-HTT gene (5-HTTLPR) has been associated with several psychiatric disorders as well as anxiety-related personality traits. In search of a mechanistic understanding of the functional implications of 5-HTTLPR, the influence of this polymorphism on regional 5-HT1A receptor density has previously been examined in two positron emission tomography (PET) studies in humans, yielding, however, contradictory results. In the present study, 54 control subjects were examined with [11C]WAY 100635 PET and a battery of cognitive tests. Regional binding potential (BP) of [11C]WAY 100635 to 5-HT1A receptor was calculated for the dorsal raphe nuclei, the hippocampus, the anterior cingulate, the insula, the temporal cortex and the frontal cortex. The influence of 5-HTTLPR genotype on regional 5-HT1A BP and cognitive performance was investigated. No differences in 5-HT1A receptor density between carriers and non-carriers of the S allele were found. Thus, we could not replicate any of the previously reported associations between 5-HTTLPR and 5-HT1A density. There was, however, a highly significant association between 5-HTTLPR genotype and performance in Wisconsin Card Sorting Test; carriers of the S allele had a superior performance compared to the LL carriers. These observations suggest that functional implications of the 5-HTTLPR polymorphism are not likely to be mediated by differences in 5-HT1A expression levels and that other biomarkers must be considered for future investigations at phenotype level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Analysis of Variance
  • Brain / anatomy & histology
  • Brain / diagnostic imaging
  • Brain / metabolism
  • Brain Mapping
  • Cognition / physiology*
  • Female
  • Genotype
  • Humans
  • Magnetic Resonance Imaging / methods
  • Male
  • Middle Aged
  • Neuropsychological Tests
  • Piperazines / metabolism
  • Polymorphism, Genetic*
  • Positron-Emission Tomography / methods
  • Protein Binding / physiology
  • Pyridines / metabolism
  • Receptor, Serotonin, 5-HT1A / metabolism*
  • Serotonin Plasma Membrane Transport Proteins / genetics*
  • Sex Factors
  • Statistics as Topic
  • Tritium / metabolism
  • Young Adult

Substances

  • Piperazines
  • Pyridines
  • Serotonin Plasma Membrane Transport Proteins
  • Tritium
  • Receptor, Serotonin, 5-HT1A
  • N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide