Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population
<p>Abstract</p> <p>Background</p> <p>Tryptophan hydroxylase-2 (TPH2) is a potential candidate gene for screening tic disorder (TD).</p> <p>Methods</p> <p>A case–control study was performed to examine the association between the TPH2 gene and TD....
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doaj-0179eb3471fe44f4ba8cb16ec8478b3f2020-11-25T00:14:38ZengBMCBehavioral and Brain Functions1744-90812013-01-0191610.1186/1744-9081-9-6Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han populationZheng PingLi ErzhenWang JianhuaCui XiaodaiWang Liwen<p>Abstract</p> <p>Background</p> <p>Tryptophan hydroxylase-2 (TPH2) is a potential candidate gene for screening tic disorder (TD).</p> <p>Methods</p> <p>A case–control study was performed to examine the association between the TPH2 gene and TD. The Sequenom® Mass ARRAY iPLEX GOLD System was used to genotype two single nucleotide polymorphisms (SNPs) of the TPH2 gene in 149 TD children and in 125 normal controls.</p> <p>Results</p> <p>For rs4565946, individuals with the TT genotype showed a significantly higher risk of TD than those with TC plus CC genotypes [odds ratio (OR) =3.077, 95% confidence interval (CI): 1.273–7.437; <it>P</it> = 0.009], as did male TD children with the TT genotype (OR = 3.228, 95% CI: 1.153–9.040; <it>P</it> = 0.020). The G allele of rs4570625 was significantly more frequent in TD children with higher levels of tic symptoms (Yale Global Tic Severity Scale, YGTSS) than those in controls among the male children (OR = 1.684, 95%: 1.097–2.583; <it>P</it> = 0.017]. TD children with severe tic symptoms had significantly higher frequencies of rs4546946 TT genotype than did normal controls in boys (OR = 3.292, 95% CI: 1.139–9.513; <it>P</it> = 0.022). We also found that genotype distributions of both SNPs were different between the Asian and European populations.</p> <p>Conclusions</p> <p>Our results indicated that the TT genotype of rs4565946 is a potential genetic risk factor for TD, and the allele G of rs4570625 might be associated with the severity of tic symptoms in boys. These polymorphisms might be susceptibility loci for TD in the Chinese Han population. Because of the confounding of co-existing attention deficit hyperactivity disorder (ADHD),these findings need to be confirmed by studies in much larger samples.</p> http://www.behavioralandbrainfunctions.com/content/9/1/6Tic disorderTryptophan hydroxylase 2Single nucleotide polymorphisms |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zheng Ping Li Erzhen Wang Jianhua Cui Xiaodai Wang Liwen |
spellingShingle |
Zheng Ping Li Erzhen Wang Jianhua Cui Xiaodai Wang Liwen Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population Behavioral and Brain Functions Tic disorder Tryptophan hydroxylase 2 Single nucleotide polymorphisms |
author_facet |
Zheng Ping Li Erzhen Wang Jianhua Cui Xiaodai Wang Liwen |
author_sort |
Zheng Ping |
title |
Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population |
title_short |
Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population |
title_full |
Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population |
title_fullStr |
Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population |
title_full_unstemmed |
Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population |
title_sort |
involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in chinese han population |
publisher |
BMC |
series |
Behavioral and Brain Functions |
issn |
1744-9081 |
publishDate |
2013-01-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Tryptophan hydroxylase-2 (TPH2) is a potential candidate gene for screening tic disorder (TD).</p> <p>Methods</p> <p>A case–control study was performed to examine the association between the TPH2 gene and TD. The Sequenom® Mass ARRAY iPLEX GOLD System was used to genotype two single nucleotide polymorphisms (SNPs) of the TPH2 gene in 149 TD children and in 125 normal controls.</p> <p>Results</p> <p>For rs4565946, individuals with the TT genotype showed a significantly higher risk of TD than those with TC plus CC genotypes [odds ratio (OR) =3.077, 95% confidence interval (CI): 1.273–7.437; <it>P</it> = 0.009], as did male TD children with the TT genotype (OR = 3.228, 95% CI: 1.153–9.040; <it>P</it> = 0.020). The G allele of rs4570625 was significantly more frequent in TD children with higher levels of tic symptoms (Yale Global Tic Severity Scale, YGTSS) than those in controls among the male children (OR = 1.684, 95%: 1.097–2.583; <it>P</it> = 0.017]. TD children with severe tic symptoms had significantly higher frequencies of rs4546946 TT genotype than did normal controls in boys (OR = 3.292, 95% CI: 1.139–9.513; <it>P</it> = 0.022). We also found that genotype distributions of both SNPs were different between the Asian and European populations.</p> <p>Conclusions</p> <p>Our results indicated that the TT genotype of rs4565946 is a potential genetic risk factor for TD, and the allele G of rs4570625 might be associated with the severity of tic symptoms in boys. These polymorphisms might be susceptibility loci for TD in the Chinese Han population. Because of the confounding of co-existing attention deficit hyperactivity disorder (ADHD),these findings need to be confirmed by studies in much larger samples.</p> |
topic |
Tic disorder Tryptophan hydroxylase 2 Single nucleotide polymorphisms |
url |
http://www.behavioralandbrainfunctions.com/content/9/1/6 |
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1725389562828554240 |