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注意缺陷多动障碍中哌甲酯反应的药物遗传学:与多巴胺转运体基因(SLC6A3)的关联

Pharmacogenetics of methylphenidate response in attention deficit/hyperactivity disorder: association with the dopamine transporter gene (SLC6A3).

作者信息

Purper-Ouakil D, Wohl M, Orejarena S, Cortese S, Boni C, Asch M, Mouren M C, Gorwood P

机构信息

AP-HP, Robert Debré Hospital, Paris, France.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1425-30. doi: 10.1002/ajmg.b.30809.

Abstract

Pharmacogenetic studies investigating the 40-bp VNTR polymorphism at SLC6A3 and methylphenidate response have shown conflicting results and large differences in study design and efficacy endpoints. Our objective was to investigate the relation between the 3'-VNTR at SLC6A3 and variability in methylphenidate response in a sample of 141 ADHD children and adolescents, assessed before and after methylphenidate treatment with both clinical and neuropsychological outcome measures. 10-R homozygotes were significantly overrepresented in the low response group, but no genotype effect was shown in cognitive variables improvement. A meta-analysis of pharmacogenetic studies with comparable data (responders vs. non-responders) on a total of 475 subjects showed a significant association between the 10-10 genotype and low rates of methylphenidate response (mean Odds Ratio = 0.46; 95% CI [0.28-0.76]). Heterogeneity between these studies did not reach a significant level but, as publications with different endpoints were excluded from this meta-analysis, our results do not rule out a possible influence of study design.

摘要

研究SLC6A3基因40bp可变数目串联重复序列(VNTR)多态性与哌甲酯反应的药物遗传学研究结果相互矛盾,且在研究设计和疗效终点方面存在很大差异。我们的目的是在141名多动症儿童和青少年样本中,研究SLC6A3基因3'-VNTR与哌甲酯反应变异性之间的关系,使用临床和神经心理学结局指标对哌甲酯治疗前后进行评估。低反应组中10-R纯合子的比例显著过高,但在认知变量改善方面未显示出基因型效应。对总共475名受试者的具有可比数据(反应者与无反应者)的药物遗传学研究进行的荟萃分析表明,10-10基因型与哌甲酯低反应率之间存在显著关联(平均优势比=0.46;95%置信区间[0.28-0.76])。这些研究之间的异质性未达到显著水平,但由于该荟萃分析排除了具有不同终点的出版物,我们的结果不能排除研究设计可能产生的影响。

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