首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder.
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Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder.

机译:成人注意缺陷多动障碍中多巴胺D5受体基因(DRD5)的研究。

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摘要

Several lines of evidence from neuroimaging, pharmacology and genetics support the involvement of the dopaminergic system in the etiology of Attention Deficit Hyperactivity Disorder (ADHD). Previous candidate gene studies have investigated the association between a dinucleotide (CA)(n) repeat polymorphism, located 18.5 kb from the start codon of the DRD5 gene, and ADHD. Association between the 148 bp allele and ADHD has been reported in some studies, however replication of the finding has not been consistent. We tested for an association between the (CA)(n) repeat and adult ADHD in a sample comprised of 119 families with adult ADHD probands and 88 unrelated adult ADHD cases with a corresponding number of controls matched for age, ethnicity and sex. In the family sample we found a non-significant trend for association between the 148 bp allele and ADHD (Z=1.91, p=0.055). An excess of non-transmissions was detected for the 150 and 152bp alleles (Z=-2.26, p=0.023; Z=-2.20, p=0.028). Quantitative analysis performed using the Brown Attention Deficit Disorder Scale (BADDS) showed association between the 150 bp allele and lower total score (p=0.011), and lower effort (p=0.008), activation (p=0.008) and attention (p=0.01) cluster scores. We did not replicate association findings in the case-control group, likely due to the lack of statistical power of this sample. Our findings add to the literature suggesting DRD5 (CA)(n) repeat has a modest effect in modulating susceptibility to adult ADHD but further studies are required.
机译:来自神经影像学,药理学和遗传学的几条证据支持多巴胺能系统参与注意力缺陷多动障碍(ADHD)的病因。先前的候选基因研究已经研究了距DRD5基因起始密码子18.5 kb的二核苷酸(CA)(n)重复多态性与ADHD的关联。在一些研究中已经报道了148 bp等位基因与ADHD之间的关联,但是该发现的重复性并不一致。我们在一个样本中测试了(CA)(n)重复与成人ADHD之间的关联,该样本包括119个有成人ADHD先证者的家庭和88个无关的成人ADHD病例,并有相应数量的对照进行了年龄,种族和性别的匹配。在家庭样本中,我们发现148 bp等位基因与ADHD之间的关联趋势不显着(Z = 1.91,p = 0.055)。对于150和152bp等位基因检测到过量的非传输(Z = -2.26,p = 0.023; Z = -2.20,p = 0.028)。使用布朗注意缺陷障碍量表(BADDS)进行的定量分析显示,150 bp等位基因与较低的总分(p = 0.011)和较低的努力(p = 0.008),激活(p = 0.008)和注意力(p = 0.01)聚类得分。我们没有在病例对照组中重复关联发现,可能是由于该样本缺乏统计能力所致。我们的发现增加了文献资料,表明DRD5(CA)(n)重复在调节成人ADHD易感性方面具有适度的作用,但需要进一步的研究。

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