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[对患有注意力缺陷障碍的哥伦比亚儿童的脑源性神经营养因子(BDNF)、儿茶酚-O-甲基转移酶(COMT)、多巴胺转运体1(DAT1)和5-羟色胺转运体(SERT)基因中的遗传变异的研究]

[Study of genetic variants in the BDNF, COMT, DAT1 and SERT genes in Colombian children with attention deficit disorder].

作者信息

Ortega-Rojas Jenny, Arboleda-Bustos Carlos E, Morales Luis, Benítez Bruno A, Beltrán Diana, Izquierdo Álvaro, Arboleda Humberto, Vásquez Rafael

机构信息

Grupo de Neurociencias, Facultad de Medicina, Universidad Nacional de Colombia, Bogotá, Colombia; Instituto de Genética, Universidad Nacional de Colombia, Bogotá, Colombia.

Grupo de Neurociencias, Facultad de Medicina, Universidad Nacional de Colombia, Bogotá, Colombia; Instituto de Genética, Universidad Nacional de Colombia, Bogotá, Colombia.

出版信息

Rev Colomb Psiquiatr. 2017 Oct-Dec;46(4):222-228. doi: 10.1016/j.rcp.2016.08.006. Epub 2016 Sep 30.

Abstract

BACKGROUND

Attention deficit and hyperactive disorder (ADHD) is highly prevalent among children in Bogota City. Both genetic and environmental factors play a very important role in the etiology of ADHD. However, to date few studies have addressed the association of genetic variants and ADHD in the Colombian population.

OBJECTIVES

To test the genetic association between polymorphisms in the DAT1, HTTLPR, COMT and BDNF genes and ADHD in a sample from Bogota City.

METHODS

We genotyped the most common polymorphisms in DAT1, SERT, COMT and BDNF genes associated with ADHD using conventional PCR followed by restriction fragment length polymorphism (RFLP) in 97 trios recruited in a medical center in Bogota. The transmission disequilibrium test (TDT) was used to determine the association between such genetic variants and ADHD.

RESULTS

The TDT analysis showed that no individual allele of any variant studied has a preferential transmission.

CONCLUSIONS

Our results suggest that the etiology of the ADHD may be complex and involves several genetic factors. Further studies in other candidate polymorphisms in a larger sample size will improve our knowledge of the ADHD in Colombian population.

摘要

背景

注意缺陷多动障碍(ADHD)在波哥大市儿童中极为普遍。遗传和环境因素在ADHD的病因中均起着非常重要的作用。然而,迄今为止,很少有研究探讨哥伦比亚人群中基因变异与ADHD的关联。

目的

在来自波哥大市的样本中,检测多巴胺转运体1(DAT1)、5-羟色胺转运体基因连锁多态性区域(HTTLPR)、儿茶酚-O-甲基转移酶(COMT)和脑源性神经营养因子(BDNF)基因多态性与ADHD之间的遗传关联。

方法

我们对97个三联体进行了常规聚合酶链反应(PCR)及随后的限制性片段长度多态性(RFLP)分析,以对DAT1、5-羟色胺转运体(SERT)、COMT和BDNF基因中与ADHD相关的最常见多态性进行基因分型,这些三联体来自波哥大的一个医疗中心。采用传递不平衡检验(TDT)来确定此类基因变异与ADHD之间的关联。

结果

TDT分析表明,所研究的任何变异的单个等位基因均无优先传递现象。

结论

我们的结果表明,ADHD的病因可能很复杂,涉及多种遗传因素。对更大样本量的其他候选多态性进行进一步研究,将增进我们对哥伦比亚人群中ADHD的了解。

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