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Association between GABA3 Gene Polymorphisms and Attention Deficit Hyperactivity Disorder in Korean Children

机译:GABA3基因多态性与韩国儿童注意缺陷多动障碍之间的关联。

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Objective Attention deficit hyperactivity disorder (ADHD) is common disorder of the school-age population. ADHD is familial and genetic studies estimate heritability at 80–90%. The aim of the present study was to investigate the association between the genetic type and alleles for gamma-aminobutyric acid receptor subunit beta-3 (GABA3) gene in Korean children with ADHD. Methods The sample consisted of 180 ADHD children and 159 control children. We diagnosed ADHD according to DSM-IV. ADHD symptoms were evaluated with Conners' Parent Rating Scales and Dupaul Parent ADHD Rating Scales. Blood samples were taken from the 339 subjects, DNA was extracted from blood lymphocytes, and PCR was performed for GABA3 rs2081648, rs1426217 and rs981778 Polymorphism. Alleles and genotype frequencies were compared using the chi-square test. We compared the allele and genotype frequencies of GABA3 gene polymorphism in the ADHD and control groups. Results This study showed that there was a significant correlation among the frequencies of the rs2081648 (OR=0.71, 95% CI=0.51–0.98, p=0.040) of alleles of MAO, but the final conclusions are not definite. Follow up studies with larger patient or pure subgroups are expected. Conclusion These results suggested that GABA3 might be related to ADHD symptoms.
机译:目的注意缺陷多动障碍(ADHD)是学龄人群的常见疾病。 ADHD是家族性的,遗传研究估计遗传率在80-90%之间。本研究的目的是调查韩国多动症儿童γ-氨基丁酸受体亚基β-3(GABA3)基因的遗传类型与等位基因之间的关联。方法样本由180名ADHD儿童和159名对照儿童组成。我们根据DSM-IV诊断出多动症。使用Conners的父母评定量表和Dupaul父母ADHD评定量表评估ADHD症状。从339名受试者中采集血样,从血液淋巴细胞中提取DNA,并对GABA3 rs2081648,rs1426217和rs981778多态性进行PCR。使用卡方检验比较等位基因和基因型频率。我们比较了ADHD组和对照组中GABA3基因多态性的等位基因和基因型频率。结果本研究表明,MAO等位基因rs2081648的频率(OR = 0.71,95%CI = 0.51–0.98,p = 0.040)之间存在显着相关性,但最终结论尚不确定。预期对较大患者或纯亚组的随访研究。结论这些结果提示GABA3可能与ADHD症状有关。

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