DRD4 Gene Polymorphisms as a Risk Factor for Children with Attention Deficit Hyperactivity Disorder in Iranian Population.

International Scholarly Research Notices Pub Date : 2017-05-24 eCollection Date: 2017-01-01 DOI:10.1155/2017/2494537
Seyed Mahmoud Tabatabaei, Shahrokh Amiri, Sara Faghfouri, Seyed Gholamreza Noorazar, Shahin AbdollahiFakhim, Ali Fakhari
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引用次数: 12

Abstract

Background and objective: Dopamine dysfunction is known to be associated with attention deficit hyperactivity disorder (ADHD). Dopamine D4 receptor gene (DRD4) is one of the important genes in this pathway. This study intended to investigate the variable number of tandem repeats (VNTR) in exon 3 of the DRD4 gene in Iranian children and adolescents.

Materials and methods: In this study, 130 children with ADHD, aged 6-14 years, and 130 healthy children, within the same age range, were enrolled. All children were selected from northwest of Iran which have Caucasian ethnic background and are of a Turkic ethnic group. VNTR polymorphisms of the DRD4 gene were evaluated by PCR using exon 3-specific primers followed by agarose gel electrophoresis.

Findings: The Hardy-Weinberg principle and Chi-square test showed a significant difference in 4-repetition (4R) alleles between the ADHD (76.2%) and control (53.8%) groups (p = 0.004; X2 = 17.39; df = 5). The least percentage of repetition alleles in both groups was 2R.

Conclusion: There is a significant correlation between the 4R alleles of DRD4 and ADHD in the northwest of Iran.

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DRD4基因多态性是伊朗人群中儿童注意缺陷多动障碍的危险因素
背景和目的:多巴胺功能障碍与注意缺陷多动障碍(ADHD)有关。多巴胺D4受体基因(DRD4)是该通路的重要基因之一。本研究旨在调查伊朗儿童和青少年DRD4基因外显子3的串联重复序列(VNTR)的可变数量。材料与方法:本研究纳入130例6-14岁ADHD儿童和130例相同年龄的健康儿童。所有儿童均来自伊朗西北部,具有高加索民族背景,属于突厥民族。利用外显子3特异性引物和琼脂糖凝胶电泳对DRD4基因的VNTR多态性进行了PCR评价。结果:Hardy-Weinberg原理和卡方检验显示ADHD组(76.2%)和对照组(53.8%)的4重复(4R)等位基因差异有统计学意义(p = 0.004;X2 = 17.39;df = 5)。两组重复等位基因的最小百分比均为2R。结论:伊朗西北部地区DRD4 4R等位基因与ADHD存在显著相关性。
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