首页> 外文期刊>Genetic testing and molecular biomarkers >Association Between HTR1A Gene Polymorphisms and Attention Deficit Hyperactivity Disorder in Korean Children;
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Association Between HTR1A Gene Polymorphisms and Attention Deficit Hyperactivity Disorder in Korean Children;

机译:HTR1A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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摘要

Attention deficit hyperactivity disorder (ADHD) is a common disorder of the school age population. ADHD has been shown to be familial, and genetic studies estimate its heritability at 80%-90%. The aim of the present study was to investigate the association between the genetic type and alleles for the HTR1A gene in Korean children with ADHD. The sample consisted of 142 ADHD children and 139 control children. We diagnosed ADHD according to the Diagnostic and Statistical Manual of Mental Disorders-4th edition. ADHD symptoms were evaluated with Conners' Parent Rating Scales and Dupaul Parent ADHD Rating Scales. Blood samples were taken from the 281 subjects, DNA was extracted from blood lymphocytes, and polymerase chain reaction was performed for HTR1A polymorphism. Alleles and genotype frequencies were compared using the chi-square test. We compared the allele and genotype frequencies of HTR1A gene polymorphism in the ADHD and control groups. This study showed that there was a significant correlation among the frequencies of the rsl0042486 (OR = 1.55, 95% CI =1.02-2.30, p = 0.041), rs1423691(OR = 1.55, 95% CI = 1.02-2.30, p = 0.041),and rs878567(OR=1.60, 95% CI=1.06-2.43, p = 0.027) alleles of HTR1A, but the final conclusions are not definite. Follow-up studies with larger patient or pure subgroups are expected. These results suggested that HTR1A might be related to ADHD symptoms.
机译:注意缺陷多动障碍(ADHD)是学龄人群的常见疾病。多动症已被证明是家族性的,遗传研究估计其遗传力为80%-90%。本研究的目的是调查韩国多动症儿童HTR1A基因的遗传类型与等位基因之间的关联。样本由142名ADHD儿童和139名对照儿童组成。我们根据《精神疾病诊断和统计手册》第4版诊断了多动症。用Conners父母父母评定量表和Dupaul父母ADHD评定量表评估ADHD症状。从281名受试者中采集血样,从血淋巴细胞中提取DNA,并进行HTR1A多态性的聚合酶链反应。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HTR1A基因多态性的等位基因和基因型频率。这项研究表明rsl0042486的频率之间存在显着相关性(OR = 1.55,95%CI = 1.02-2.30,p = 0.041),rs1423691(rs = 1.55,95%CI = 1.02-2.30,p = 0.041) )和rs878567(OR = 1.60,95%CI = 1.06-2.43,p = 0.027)等位基因,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。这些结果表明HTR1A可能与ADHD症状有关。

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  • 来源
    《Genetic testing and molecular biomarkers》 |2013年第3期|178-182|共5页
  • 作者单位

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea,Eumseong Somang Hospital, Eumseong, South Korea;

    Department of Psychiatry, College of Medicine, Dankook University, Cheonan City, South Korea;

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea,Department of Preventive Medicine, College of Medicine, Dankook University, Cheonan City, South Korea;

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea,Department of Preventive Medicine, College of Medicine, Dankook University, Cheonan City, South Korea;

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea;

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea;

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea,Department of Psychiatry, College of Medicine, Dankook University, Cheonan City, South Korea;

    Environmental Health Center, Dankook Medical Hospital, Cheonan City, South Korea,Department of Psychiatry College of Medicine Dankook University Manghyang Rho 359 Cheonan City 330-715 South Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
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  • 正文语种 eng
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