Further evidence of association between two NET single-nucleotide polymorphisms with ADHD

被引:41
|
作者
Kim, J. W. [1 ]
Biederman, J.
McGrath, C. L. [1 ]
Doyle, A. E.
Mick, E.
Fagerness, J. [1 ]
Purcell, S. [1 ]
Smoller, J. W. [1 ]
Sklar, P. [1 ]
Faraone, S. V. [2 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Ctr Human Genet Res, Psychiat & Neurodev Genet Unit,Med Sch, Boston, MA 02114 USA
[2] SUNY Upstate Med Univ, Dept Psychiat, Syracuse, NY USA
关键词
ADHD; NET; association; SNP; replication;
D O I
10.1038/sj.mp.4002090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The norepinephrine transporter (NET) gene is an attractive candidate gene for attention-deficit hyperactivity disorder (ADHD). Noradrenergic systems are critical to higher brain functions such as attention and executive function, which are defective in ADHD. The clinical efficacy of medications that target NET also supports its role in the etiology of ADHD. Here, we have applied a dense mapping strategy to capture all genetic variations within the NET gene in a large number of ADHD families (474 trios). As a result, we found association of the same alleles from two single-nucleotide polymorphisms (rs3785143 and rs11568324) previously identified in another large-scale ADHD genetic study (International Multisite ADHD Geneproject). Furthermore, the effect sizes were consistent across both studies. This is the first time that identical alleles of NET from different studies were implicated, and thus our report provides further evidence that the NET gene is involved in the etiology of ADHD.
引用
收藏
页码:624 / 630
页数:7
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