【目的】 分析儿童注意缺陷多动障碍(attention deficit hyperactivity disorder, ADHD)与儿茶酚-O-甲基转移酶(catechol-O-methyltransferase, COMT)基因第158位密码子G→A点突变所引起的缬氨酸→甲硫氨酸(Val158Met)的错义突变多态性的关系。 【方法】 采用实时荧光定量PCR技术,分析了110例ADHD儿童与90例正常儿童COMT基因Val158Met多态性的位点频率。 【结果】 病例组A等位基因的频率为22.73%,而对照组为23.33%,两组差异无统计学意义(χ2=0.021,P>0.05)。COMT各基因型的分布频率在病例组和对照组之间差异也无统计学意义(χ2=3.668,P>0.05)。 【结论】 COMT基因Val158Met多态性可能与儿童ADHD无关联。
Abstract
【Objective】 To analyze the correlation between attention deficit hyperactivity disorder(ADHD) in children and Val158Met polymorphism of catechol-O-methyltransferase(COMT) gene caused by the missense mutation of G158A. 【Methods】 The Val158Met polymorphism of COMT gene was tested in 110 children with ADHD and 90 non-ADHD by using quantitative PCR technique. 【Results】 The frequencies of A allele were 22.73% and 23.33% in case and controlled group respectively, which showed no significant difference between the two groups(χ2=0.021,P>0.05). There was also no significant difference in the distribution of all genotypes of COMT gene between the two groups(χ2=3.668,P>0.05). 【Conclusions】 It is suggested that there is no association between ADHD in children and Val158Met polymorphism of COMT gene in this study.
关键词
注意缺陷多动障碍 /
儿茶酚-O-甲基转移酶 /
遗传多态性
Key words
attention deficit hyperactivity disorder /
catechol-O-methyl transferase /
genetic polymorphism
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参考文献
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基金
湖北省卫生厅青年科技人才基金资助项目(QJX2005-12)
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