Arcos-Burgos M, Castellanos F X, Konecki D, Lopera F, Pineda D, Palacio J D, Rapoport J L, Berg K, Bailey-Wilson J, Muenke M
National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-1852, USA.
Mol Psychiatry. 2004 Mar;9(3):252-9. doi: 10.1038/sj.mp.4001396.
Association/linkage between dopamine D4 receptor (DRD4) polymorphisms and attention-deficit/hyperactivity disorder (ADHD) has been suggested by case-control- and nuclear-family-based studies. Here, we present a candidate gene analysis for DRD4 using 14 extended and multigenerational families segregating ADHD derived from the 'Paisa' community of Antioquia, Colombia, a genetic isolate. Two DRD4 polymorphisms (a 120 bp tandem duplication at the promoter and a 48 bp-VNTR at exon 3), reported associated to ADHD, were genotyped. Parametric and non-parametric linkage analyses, and a family-based association test (FBAT), the pedigree disequilibrium test (PDT), were applied to search for evidence of association/linkage. Two-point LOD scores were significantly negative, with values ranging from -3.21 (P=0.011158) to -7.66 (P=0.000091 at theta=0). Non-parametrical analysis resulted in nonsignificant evidence for linkage. The PDT showed a moderate trend toward significance of association/linkage between the 7-repeat (7R) allele at the 48 bp VNTR and ADHD (P=0.0578). Furthermore, the haplotype analysis shows a significant association/linkage of the 7R-240 bp haplotype (P=0.0467) with ADHD. Results suggest that either a moderate DRD4 genetic effect, or linkage disequilibrium of DRD4 with an ADHD disease locus in the vicinity or the linkage to a phenotypic component of the ADHD spectrum could be underlying this association/linkage. These results provide further evidence for the association of ADHD to genetic variation in or near to DRD4 and replicate the previously reported association between ADHD and the 7R allele.
基于病例对照研究和核心家庭研究,已表明多巴胺D4受体(DRD4)基因多态性与注意力缺陷多动障碍(ADHD)之间存在关联/连锁。在此,我们对来自哥伦比亚安蒂奥基亚省“派萨”社区(一个遗传隔离群体)的14个患有ADHD的扩展性多代家庭进行了DRD4候选基因分析。对两个已报道与ADHD相关的DRD4基因多态性(启动子区120bp串联重复和外显子3区48bp可变数目串联重复序列(VNTR))进行了基因分型。应用参数和非参数连锁分析以及基于家系的关联检验(FBAT)、家系不平衡检验(PDT)来寻找关联/连锁的证据。两点连锁分析的LOD值显著为负,范围从-3.21(P = 0.011158)到-7.66(在θ = 0时,P = 0.000091)。非参数分析未得出显著的连锁证据。PDT显示48bp VNTR的7重复(7R)等位基因与ADHD之间存在关联/连锁的中度显著趋势(P = 0.0578)。此外,单倍型分析显示7R - 240bp单倍型与ADHD存在显著关联/连锁(P = 0.0467)。结果表明,可能是DRD4适度的遗传效应,或者DRD4与附近ADHD疾病位点的连锁不平衡,又或者是与ADHD谱系表型成分的连锁,构成了这种关联/连锁的基础。这些结果为ADHD与DRD4或其附近基因变异的关联提供了进一步证据,并重复了先前报道的ADHD与7R等位基因之间的关联。