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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Association of glutathione S-transferases M1, T1 and P1 gene polymorphisms with attention deficit and hyperactivity disorder in Korean children
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Association of glutathione S-transferases M1, T1 and P1 gene polymorphisms with attention deficit and hyperactivity disorder in Korean children

机译:谷胱甘肽S-转移酶M1,T1和P1基因多态性与韩国儿童注意缺陷和多动障碍的关系

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摘要

Attention deficit and hyperactivity disorder (ADHD) is highly heritable disorder and common in school-age children characterized by inattention, hyperactivity and impulsivity. Although its heritability was estimated at 80-90% from family, adoption and twin studies, the molecular etiology of this disorder has not elucidated. Meanwhile, an impaired balance of oxidant-antioxidant status and increased oxidative stress is observed in ADHD, and it may imply a possible relationship between oxidative stress and etiology of ADHD. Glutathione S-transferase (GST) is antioxidant enzymes that play a key role in the cellular detoxification. In the present study, we examined the association between the genetic polymorphisms of GSTM1, GSTP1 and GSTT1, and ADHD in Korean children. Case-control study was conducted with 243 ADHD children and 327 controls. There were no significant associations between the polymorphisms and the incidence of ADHD (p>0.05). However, significant associations were observed in the stratified analyses. The frequency of GSTP1 Ile/Ile genotype is reached to the significant level in the hyperactivity subtype (88.2%) compared to controls (64.8%) (p = 0.035) and the frequency of GSTT1-null genotype is significantly higher in the inattentive boys (p = 0.005). Similarly, GSTT1-null genotype showed significant associations in combined subtype (p = 0.016) and hyperactivity subtype (p = 0.036) of the ADHD girls. Thus our result imply that the polymorphisms in the GST genes may affect ADHD, however, replication study for larger sample set and functional studies are crucial to confirm these findings. (C) 2016 Elsevier B.V. All rights reserved.
机译:注意缺陷和多动障碍(ADHD)是高度可遗传的疾病,常见于学龄儿童,其特征为注意力不集中,多动和冲动。尽管从家庭,收养和双生子研究中估计其遗传力为80-90%,但尚未阐明该疾病的分子病因。同时,在ADHD中观察到氧化-抗氧化剂状态的平衡受损和氧化应激增加,这可能暗示氧化应激与ADHD病因之间可能存在关系。谷胱甘肽S-转移酶(GST)是抗氧化酶,在细胞排毒中起关键作用。在本研究中,我们检查了韩国儿童中GSTM1,GSTP1和GSTT1和ADHD遗传多态性之间的关联。对243名ADHD儿童和327名对照进行了病例对照研究。多态性与ADHD的发生率之间无显着相关性(p> 0.05)。但是,在分层分析中观察到显着的关联。 GSTP1 Ile / Ile基因型的频率在多动症亚型中达到显着水平(88.2%),而对照组(64.8%)(p = 0.035),而注意力不集中的男孩中GSTT1空基因型的频率显着更高( p = 0.005)。同样,GSTT1无效基因型在多动症女孩的合并亚型(p = 0.016)和多动症亚型(p = 0.036)中显示显着关联。因此,我们的结果暗示GST基因中的多态性可能会影响ADHD,但是,对较大样本集进行的复制研究和功能研究对于确认这些发现至关重要。 (C)2016 Elsevier B.V.保留所有权利。

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