Chang-Hong Wang, Qiu-Fen Ning, Cong Liu, Ting-Ting Lv, En-Zhao Cong, Jing-Yang Gu, Ying-Li Zhang, Hui-Yao Nie, Xiao-Li Zhang, Yan Li, Xiang-Yang Zhang, Lin-Yan Su
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The purposes of this study were to investigate the potential association of 5-HTT gene promoter polymorphism (5-HTTLPR) and MAOA gene polymorphism with susceptibility to ODD in a Han Chinese school population.</p><p><strong>Methods: </strong>The 5-HTTLPR gene polymorphism and the MAOA gene polymorphism were genotyped in a case-control study of 257 Han Chinese children (123 ODD and 134 healthy controls).</p><p><strong>Results: </strong>There was significant difference in the allele distribution of 5-HTTLPR (χ<sup>2</sup> = 7.849, P = 0.005) between the ODD and control groups. Further, there were significant differences in genotype (χ<sup>2</sup> = 5.168, P = 0.023) and allele distributions (χ<sup>2</sup> = 10.336, P = 0.001) of the MAOA gene polymorphism that is variable-number tandem repeat (MAOA-uVNTR) between two groups. Moreover, there were significant differences in genotype (χ<sup>2</sup> = 4.624, P = 0.032) and allele distributions (χ<sup>2</sup> = 9.248, P = 0.002) of MAOA-uVNTR only in the male ODD and healthy groups.</p><p><strong>Conclusions: </strong>Our results suggest that 5-HTTLPR and MAOA-uVNTR gene variants may contribute to susceptibility to ODD. Further, MAOA-uVNTR gene polymorphism may play a role in susceptibility to ODD only in male children.</p>","PeriodicalId":8729,"journal":{"name":"Behavioral and Brain Functions","volume":"14 1","pages":"15"},"PeriodicalIF":4.7000,"publicationDate":"2018-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12993-018-0147-6","citationCount":"5","resultStr":"{\"title\":\"Associations of serotonin transporter gene promoter polymorphisms and monoamine oxidase A gene polymorphisms with oppositional defiant disorder in a Chinese Han population.\",\"authors\":\"Chang-Hong Wang, Qiu-Fen Ning, Cong Liu, Ting-Ting Lv, En-Zhao Cong, Jing-Yang Gu, Ying-Li Zhang, Hui-Yao Nie, Xiao-Li Zhang, Yan Li, Xiang-Yang Zhang, Lin-Yan Su\",\"doi\":\"10.1186/s12993-018-0147-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Oppositional defiant disorder (ODD) is a behavioral disorder that mainly refers to a recurrent pattern of disobedient, defiant, negativistic and hostile behaviors toward authority figures. Previous studies have showed associations of serotonin transporter (5-HTT) and monoamine oxidase A (MAOA) with behavioral and psychiatric disorders. The purposes of this study were to investigate the potential association of 5-HTT gene promoter polymorphism (5-HTTLPR) and MAOA gene polymorphism with susceptibility to ODD in a Han Chinese school population.</p><p><strong>Methods: </strong>The 5-HTTLPR gene polymorphism and the MAOA gene polymorphism were genotyped in a case-control study of 257 Han Chinese children (123 ODD and 134 healthy controls).</p><p><strong>Results: </strong>There was significant difference in the allele distribution of 5-HTTLPR (χ<sup>2</sup> = 7.849, P = 0.005) between the ODD and control groups. Further, there were significant differences in genotype (χ<sup>2</sup> = 5.168, P = 0.023) and allele distributions (χ<sup>2</sup> = 10.336, P = 0.001) of the MAOA gene polymorphism that is variable-number tandem repeat (MAOA-uVNTR) between two groups. Moreover, there were significant differences in genotype (χ<sup>2</sup> = 4.624, P = 0.032) and allele distributions (χ<sup>2</sup> = 9.248, P = 0.002) of MAOA-uVNTR only in the male ODD and healthy groups.</p><p><strong>Conclusions: </strong>Our results suggest that 5-HTTLPR and MAOA-uVNTR gene variants may contribute to susceptibility to ODD. 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引用次数: 5
摘要
背景:对立违抗性障碍(ODD)是一种行为障碍,主要指对权威人物反复出现不服从、违抗、消极和敌对行为。先前的研究表明5-羟色胺转运体(5-HTT)和单胺氧化酶A (MAOA)与行为和精神疾病有关。本研究旨在探讨中国汉族学校人群5-HTT基因启动子多态性(5-HTTLPR)和MAOA基因多态性与ODD易感性的潜在关联。方法:对257例汉族儿童(残疾儿童123例,健康儿童134例)进行5-HTTLPR基因多态性和MAOA基因多态性的病例对照研究。结果:ODD组与对照组5-HTTLPR等位基因分布差异有统计学意义(χ2 = 7.849, P = 0.005)。MAOA基因可变数串联重复序列(MAOA- uvntr)基因型(χ2 = 5.168, P = 0.023)和等位基因分布(χ2 = 10.336, P = 0.001)差异均有统计学意义。moaa - uvntr基因型(χ2 = 4.624, P = 0.032)和等位基因分布(χ2 = 9.248, P = 0.002)在男性ODD组和健康组之间存在显著差异。结论:5-HTTLPR和MAOA-uVNTR基因变异可能与ODD易感性有关。此外,MAOA-uVNTR基因多态性可能仅在男性儿童中对ODD易感性起作用。
Associations of serotonin transporter gene promoter polymorphisms and monoamine oxidase A gene polymorphisms with oppositional defiant disorder in a Chinese Han population.
Background: Oppositional defiant disorder (ODD) is a behavioral disorder that mainly refers to a recurrent pattern of disobedient, defiant, negativistic and hostile behaviors toward authority figures. Previous studies have showed associations of serotonin transporter (5-HTT) and monoamine oxidase A (MAOA) with behavioral and psychiatric disorders. The purposes of this study were to investigate the potential association of 5-HTT gene promoter polymorphism (5-HTTLPR) and MAOA gene polymorphism with susceptibility to ODD in a Han Chinese school population.
Methods: The 5-HTTLPR gene polymorphism and the MAOA gene polymorphism were genotyped in a case-control study of 257 Han Chinese children (123 ODD and 134 healthy controls).
Results: There was significant difference in the allele distribution of 5-HTTLPR (χ2 = 7.849, P = 0.005) between the ODD and control groups. Further, there were significant differences in genotype (χ2 = 5.168, P = 0.023) and allele distributions (χ2 = 10.336, P = 0.001) of the MAOA gene polymorphism that is variable-number tandem repeat (MAOA-uVNTR) between two groups. Moreover, there were significant differences in genotype (χ2 = 4.624, P = 0.032) and allele distributions (χ2 = 9.248, P = 0.002) of MAOA-uVNTR only in the male ODD and healthy groups.
Conclusions: Our results suggest that 5-HTTLPR and MAOA-uVNTR gene variants may contribute to susceptibility to ODD. Further, MAOA-uVNTR gene polymorphism may play a role in susceptibility to ODD only in male children.
期刊介绍:
A well-established journal in the field of behavioral and cognitive neuroscience, Behavioral and Brain Functions welcomes manuscripts which provide insight into the neurobiological mechanisms underlying behavior and brain function, or dysfunction. The journal gives priority to manuscripts that combine both neurobiology and behavior in a non-clinical manner.