5-HTTLPR variants not associated with autistic spectrum disorders

Neurogenetics. 1999 Apr;2(2):129-31. doi: 10.1007/s100480050064.

Abstract

To determine whether there is an association of polymorphic variants of the serotonin transporter (5-HTT) gene-linked polymorphic region (5-HTTLPR) and autistic spectrum disorders, we analyzed the 5-HTTLPR genotypes of 72 autistic subjects, 11 fragile X syndrome patients with autistic behavior, 43 normal subjects, and 49 fragile X syndrome non-autistic subjects. The distribution frequency of 5-HTTLPR long allele (L) and the short allele (S) variants showed no differences between subjects. Our findings do not support the hypothesis that polymorphic 5-HTTLPR variants are a susceptibility factor for autistic disorders.

MeSH terms

  • Alleles
  • Autistic Disorder / genetics*
  • Carrier Proteins / genetics*
  • Child
  • Ethnicity
  • Fragile X Syndrome / genetics*
  • Genetic Predisposition to Disease
  • Genetic Variation*
  • Genotype
  • Germany
  • Humans
  • Membrane Glycoproteins / genetics*
  • Membrane Transport Proteins*
  • Nerve Tissue Proteins*
  • Polymorphism, Genetic*
  • Racial Groups
  • Reference Values
  • Serotonin / genetics
  • Serotonin Plasma Membrane Transport Proteins
  • United States

Substances

  • Carrier Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins
  • Serotonin