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Possible effect of norepinephrine transporter polymorphisms on methylphenidate-induced changes in neuropsychological function in attention-deficit hyperactivity disorder

机译:去甲肾上腺素转运蛋白多态性对哌醋甲酯引起的注意力缺陷多动障碍神经心理功能变化的可能影响

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Background Dysregulation of noradrenergic system may play important roles in pathophysiology of attention-deficit/hyperactivity disorder (ADHD). We examined the relationship between polymorphisms in the norepinephrine transporter SLC6A2 gene and attentional performance before and after medication in children with ADHD. Methods Fifty-three medication-na?ve children with ADHD were genotyped and evaluated using the continuous performance test (CPT). After 8-weeks of methylphenidate treatment, these children were evaluated by CPT again. We compared the baseline CPT measures and the post-treatment changes in the CPT measures based on the G1287A and the A-3081T polymorphisms of SLC6A2. Results There was no significant difference in the baseline CPT measures associated with the G1287A or A-3081T polymorphisms. After medication, however, ADHD subjects with the G/G genotype at the G1287A polymorphism showed a greater decrease in the mean omission error scores (p?=?0.006) than subjects with the G/A or A/A genotypes, and subjects with the T allele at the A-3081T polymorphism (T/T or A/T) showed a greater decrease in the mean commission error scores (p?=?0.003) than those with the A/A genotypes. Conclusions Our results provide evidence for the possible role of the G1287A and A-3081T genotypes of SLC6A2 in methylphenidate-induced improvement in attentional performance and support the noradrenergic hypothesis for the pathophysiology of ADHD.
机译:背景去甲肾上腺素能系统的失调可能在注意缺陷/多动障碍(ADHD)的病理生理中起重要作用。我们检查了多动症儿童用药前后去甲肾上腺素转运蛋白SLC6A2基因多态性与注意力表现之间的关系。方法对53名未接受过药物治疗的多动症儿童进行基因分型,并使用持续表现测试(CPT)进行评估。哌醋甲酯治疗8周后,再次通过CPT评估了这些儿童。我们比较了基准CPT措施和基于GLC1A2的G1287A和A-3081T多态性的CPT措施的治疗后变化。结果与G1287A或A-3081T多态性相关的基线CPT指标无显着差异。但是,服药后,G1287A基因多态性为G / G基因型的ADHD受试者,其平均遗漏错误评分的下降幅度较大(p?=?0.006),高于具有G / A或A / A基因型的受试者以及A-3081T基因多态性(T / T或A / T)的T等位基因显示平均佣金错误得分的下降幅度更大(p?=?0.003)。结论我们的结果提供了SLC6A2的G1287A和A-3081T基因型在哌醋甲酯诱导的注意力改善中可能发挥的作用的证据,并支持去甲肾上腺素能假说对ADHD的病理生理作用。

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