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

Authors :
Chang-Hong Wang
Cong Liu
En-Zhao Cong
Gai-Ling Xu
Ting-Ting Lv
Ying-Li Zhang
Qiu-Fen Ning
Ji-Kang Wang
Hui-Yao Nie
Yan Li
Source :
Behavioral & Brain Functions. 11/21/2016, Vol. 12, p1-12. 12p.
Publication Year :
2016

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 (χ2 = 4.163, P = 0.041) and allele frequency (χ2 = 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17449081
Volume :
12
Database :
Academic Search Index
Journal :
Behavioral & Brain Functions
Publication Type :
Academic Journal
Accession number :
119659415
Full Text :
https://doi.org/10.1186/s12993-016-0113-0