Association of tryptophan hydroxylase-2 polymorphisms with oppositional defiant disorder in a Chinese Han population

Behav Brain Funct. 2016 Nov 21;12(1):30. doi: 10.1186/s12993-016-0113-0.

Abstract

Background: Oppositional defiant disorder (ODD) is a behavioral disorder of school-age population. It is well known that 5-HT dysfunction is correlated with impulsivity, which is one of the common characteristics of ODD. The enzyme tryptophan hydroxylase-2 (TPH-2) synthesizes 5-HT in serotonergic neurons of the midbrain raphe. The purposes of this study were to investigate the potential association of TPH-2 polymorphisms with susceptibility to ODD in a Han Chinese school population.

Methods: Four polymorphisms (rs4570625, rs11178997, rs1386494 and rs7305115) of the TPH-2 gene were analyzed by using polymerase chain reaction and DNA microarray hybridization in a case-control study of 276 Han Chinese individuals (124 ODD and 152 controls).

Results: In single marker analyses,there was a significant difference in the genotype (χ 2 = 4.163, P = 0.041) and allele frequency (χ 2 = 3.930, P = 0.047) of rs1386494 between ODD and control groups. Haplotype analyses revealed higher frequencies of haplotypes TA (rs4570625-rs11178997), TAG (rs4570625-rs11178997-rs1386494), TAA (rs4570625-rs11178997-rs7305115) and TAGA (rs4570625-rs11178997-rs1386494-rs7305115), but lower frequencies of haplotypes GA (rs4570625-rs11178997) and GAG (rs4570625-rs11178997-rs1386494) in ODD compared to control groups.

Conclusions: These findings suggest the role of these TPH-2 gene variants in susceptibility to ODD. Some haplotypes might be the risk factors for Chinese Han children with ODD, while others might be preventable factors.

Keywords: Oppositional defiant disorder; Single nucleotide polymorphisms; Tryptophan hydroxylase-2 gene.

MeSH terms

  • Adolescent
  • Asian People / genetics
  • Attention Deficit and Disruptive Behavior Disorders / enzymology*
  • Attention Deficit and Disruptive Behavior Disorders / genetics*
  • Case-Control Studies
  • Child
  • China
  • Ethnicity / genetics
  • Female
  • Gene Frequency
  • Genetic Association Studies / methods
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Linkage Disequilibrium
  • Male
  • Polymorphism, Single Nucleotide
  • Tryptophan Hydroxylase / genetics*
  • Tryptophan Hydroxylase / metabolism

Substances

  • TPH2 protein, human
  • Tryptophan Hydroxylase