Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population

Neurosci Lett. 2017 Sep 29:658:161-164. doi: 10.1016/j.neulet.2017.08.041. Epub 2017 Aug 19.

Abstract

Although Tourette syndrome (TS) is a chronic neuropsychiatric disorder whose pathogenesis remains unclear, genetic factors play an important role in the occurrence and development. A variety of studies have been shown that the candidate genes related to cholinergic neurons may be associated with the onset of TS. To investigate the association between the SLC5A7 polymorphisms and Tourette syndrome (TS) in the Chinese Han population, the SNP rs1013940, rs2433718, and rs4676169 were genotyped in 401 TS trios and 400 controls. The transmission disequilibrium test (TDT) and haplotype relative risk (HRR) compared genetic distributions of trios, while the chi-square test compared patients and controls. However, no transmission disequilibrium was found between the three SLC5A7 SNPs and TS. Therefore, we think that this gene may not be the main risk factor on the onset of TS. However, these results should be further validated in different populations.

Keywords: Case–control study; Family-based study; Haplotype relative risk; SLC5A7 gene; Tourette syndrome; Transmission disequilibrium test.

MeSH terms

  • Adolescent
  • Asian People / genetics
  • Child
  • Child, Preschool
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Linkage Disequilibrium / genetics*
  • Male
  • Polymorphism, Single Nucleotide / genetics
  • Symporters / genetics*
  • Tourette Syndrome / genetics*

Substances

  • SLC5A7 protein, human
  • Symporters