Biased paternal transmission of SNAP-25 risk alleles in attention-deficit hyperactivity disorder

被引:93
|
作者
Kustanovich, V
Merriman, B
McGough, J
McCracken, JT
Smalley, SL
Nelson, SF [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Psychiat & Biobehav Sci, Div Child & Adolescent Psychiat, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Human Genet, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Sch Med, Ctr Neurobehav Genet, Los Angeles, CA 90024 USA
关键词
attention-deficit hyperactivity disorder; ADHD; SNAP-25; genetics; neuropsychiatric genetics;
D O I
10.1038/sj.mp.4001247
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
Attention-deficit hyperactivity disorder (ADHD) is the most common childhood psychiatric disorder, affecting 5-10% of school-age children. Although the biological basis of this disorder is unknown, twin and family studies provide strong evidence that ADHD has a genetic basis involving multiple genes. A previous study found an association between ADHD and two polymorphisms in the 3' untranslated region (UTR) of SNAP-25, a gene encoding a synaptic vesicle docking protein known to play a role in the hyperactivity observed in the Coloboma mouse strain. In this paper, we test biased transmission of the 3' UTR SNAP-25 haplotype using a larger ADHI) sample of 113 families with 207 affected children. Using the transmission disequilibrium test (TDT), we found a trend consistent with biased transmission of the TC haplotype of SNAP-25 in all transmissions and detected a significant distortion (P=0.027) when paternal transmissions were evaluated.
引用
收藏
页码:309 / 315
页数:7
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