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以及注意缺陷多动障碍儿童的VNTR基因分型

and VNTR Genotyping in Children with Attention Deficit Hyperactivity Disorder.

作者信息

Stanley Ashley, Chavda K, Subramanian A, Prabhu S V, Ashavaid T F

机构信息

Research Laboratories, P. D. Hinduja Hospital and Medical Research Centre, Veer Savarkar Marg, Mahim, Mumbai, 400016 India.

Department of Medicine, P. D. Hinduja Hospital and Medical Research Centre, Veer Savarkar Marg, Mahim, Mumbai, 400016 India.

出版信息

Indian J Clin Biochem. 2017 Jun;32(2):239-242. doi: 10.1007/s12291-016-0587-4. Epub 2016 Jun 24.

DOI:10.1007/s12291-016-0587-4
PMID:28428702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5382072/
Abstract

The dopamine receptor-D4 and the dopamine transporter have been investigated for their role in attention deficit hyperactivity disorder (ADHD) in children. Reports of their genetic association with ADHD have shown mixed results. The aim of the study was to evaluate the association of variable number tandem repeats (VNTRs) of the and genes with ADHD in children. A pilot 1:1 case control study, with 44 clinically confirmed ADHD cases and 44 age/gender matched healthy controls, was conducted at a tertiary care centre in Mumbai. Variable number tandem repeats of exon 3, intron 8 and 3'UTR were genotyped by PCR-AGE. Several allele repeats of the genes were observed in the screened subjects. Statistical significance was observed for the 10R/10R genotype of the 3'UTR VNTR between cases and controls.

摘要

多巴胺受体D4和多巴胺转运体在儿童注意力缺陷多动障碍(ADHD)中的作用已得到研究。关于它们与ADHD的基因关联的报告结果不一。本研究的目的是评估儿童中 和 基因的可变数目串联重复序列(VNTRs)与ADHD的关联。在孟买的一家三级医疗中心进行了一项初步的1:1病例对照研究,有44例临床确诊的ADHD病例和44例年龄/性别匹配的健康对照。通过PCR-AGE对 外显子3、 内含子8和3'UTR的可变数目串联重复序列进行基因分型。在筛查的受试者中观察到了这些基因的几个等位基因重复。病例组和对照组之间在 3'UTR VNTR的10R/10R基因型上观察到统计学显著性。

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Iran J Psychiatry. 2024 Jan;19(1):99-106. doi: 10.18502/ijps.v19i1.14345.
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ADHD: Reviewing the Causes and Evaluating Solutions.注意力缺陷多动障碍:病因回顾与解决方案评估
J Pers Med. 2021 Mar 1;11(3):166. doi: 10.3390/jpm11030166.
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Association study and a systematic meta-analysis of the VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder.多巴胺转运体基因 3'-UTR 区 VNTR 多态性与注意缺陷多动障碍的关联研究及系统荟萃分析。
J Neural Transm (Vienna). 2019 Apr;126(4):517-529. doi: 10.1007/s00702-019-01998-x. Epub 2019 Mar 28.
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Genes Genomics. 2018 Dec;40(12):1309-1317. doi: 10.1007/s13258-018-0726-9. Epub 2018 Aug 11.

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Fitting the pieces together: current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD).将碎片拼合在一起:当前关于注意缺陷多动障碍(ADHD)遗传基础的研究。
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Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): increased prevalence of the 2-repeat allele.中国汉族注意缺陷多动障碍(ADHD)儿童的多巴胺受体D4(DRD4)基因:2重复等位基因的患病率增加
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