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Associations of serotonin transporter gene promoter polymorphisms and monoamine oxidase A gene polymorphisms with oppositional defiant disorder in a Chinese Han population

机译:血清素转运蛋白基因启动子多态性和单胺氧化酶A基因多态性与中国汉族人群对立违抗性的关联

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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. 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). 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. 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.
机译:反对抗辩障碍(ODD)是一种行为障碍,主要是指对权威人物的不服从,抗拒,消极和敌对行为的反复出现。先前的研究表明,血清素转运蛋白(5-HTT)和单胺氧化酶A(MAOA)与行为和精神疾病有关。这项研究的目的是调查在中国汉族人群中5-HTT基因启动子多态性(5-HTTLPR)和MAOA基因多态性与对ODD的易感性之间的潜在联系。在一项针对257名汉族儿童(123名ODD和134名健康对照)的病例对照研究中,对5-HTTLPR基因多态性和MAOA基因多态性进行了基因分型。在ODD组和对照组之间,5-HTTLPR的等位基因分布存在显着差异(χ2α=?7.849,P?=?0.005)。此外,可变数目串联重复的MAOA基因多态性的基因型(χ2β=?5.168,P?=?0.023)和等位基因分布(χ2?=?10.336,P?=?0.001)存在显着差异(两组之间的MAOA-uVNTR)。此外,仅在男性ODD组和健康组中,MAOA-uVNTR的基因型(χ2α=α4.624,Pα=α0.032)和等位基因分布(χ2α=α9.248,Pα= 0.002)有显着差异。我们的研究结果表明5-HTTLPR和MAOA-uVNTR基因变异可能有助于对ODD的易感性。此外,MAOA-uVNTR基因多态性可能仅在男性儿童中对ODD易感性中起作用。

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