• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

注意力缺陷多动障碍与多巴胺β-羟化酶基因

Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase.

作者信息

Wigg Karen, Zai Gwyneth, Schachar Russell, Tannock Rosemary, Roberts Wendy, Malone Molly, Kennedy James L, Barr Cathy L

机构信息

Department of Psychiatry, Toronto Western Hospital, Ont., Canada.

出版信息

Am J Psychiatry. 2002 Jun;159(6):1046-8. doi: 10.1176/appi.ajp.159.6.1046.

DOI:10.1176/appi.ajp.159.6.1046
PMID:12042196
Abstract

OBJECTIVE

Attention deficit hyperactivity disorder (ADHD) has been shown to be highly heritable, and recent molecular genetics studies have focused on candidate genes in the dopaminergic and noradrenergic systems. One recent study reported an association of an allele of the TaqI polymorphism located in the fifth intron of the gene for dopamine beta-hydroxylase (DBH). The authors' goal was to replicate this finding.

METHOD

The authors investigated the linkage of the alleles and haplotypes of three polymorphisms at the DBH locus in 117 nuclear families with ADHD.

RESULTS

No significant evidence was found for linkage of the TaqI alleles or haplotypes in the 117 families. However, the authors observed some evidence for biased transmission of the same allele of the TaqI polymorphism, as previously reported.

CONCLUSIONS

These findings suggest that the gene for DBH should be investigated further.

摘要

目的

注意力缺陷多动障碍(ADHD)已被证明具有高度遗传性,近期的分子遗传学研究聚焦于多巴胺能和去甲肾上腺素能系统中的候选基因。最近一项研究报告称,位于多巴胺β-羟化酶(DBH)基因第五内含子的TaqI多态性的一个等位基因存在关联。作者的目标是重复这一发现。

方法

作者在117个患有ADHD的核心家庭中研究了DBH基因座上三个多态性的等位基因和单倍型的连锁情况。

结果

在这117个家庭中,未发现TaqI等位基因或单倍型连锁的显著证据。然而,正如之前所报道的,作者观察到了TaqI多态性相同等位基因的偏态传递的一些证据。

结论

这些发现表明,应进一步研究DBH基因。

相似文献

1
Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase.注意力缺陷多动障碍与多巴胺β-羟化酶基因
Am J Psychiatry. 2002 Jun;159(6):1046-8. doi: 10.1176/appi.ajp.159.6.1046.
2
Lack of significant association between -1021C-->T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder.多巴胺β羟化酶基因-1021C→T多态性与注意缺陷多动障碍之间缺乏显著关联。
Neurosci Lett. 2006 Jul 10;402(1-2):12-6. doi: 10.1016/j.neulet.2006.03.036. Epub 2006 Apr 17.
3
Further evidence for the association between attention-deficit/hyperactivity disorder and the dopamine-beta-hydroxylase gene.注意缺陷多动障碍与多巴胺-β-羟化酶基因之间关联的进一步证据。
Am J Med Genet. 2002 Mar 8;114(2):154-8. doi: 10.1002/ajmg.10194.
4
Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.多巴胺β羟化酶基因多态性分析:与印度儿童注意力缺陷多动障碍的关联
Indian Pediatr. 2005 Feb;42(2):123-9.
5
Association of the dopamine beta hydroxylase gene with attention deficit hyperactivity disorder: genetic analysis of the Milwaukee longitudinal study.多巴胺β羟化酶基因与注意力缺陷多动障碍的关联:密尔沃基纵向研究的基因分析
Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):77-85. doi: 10.1002/ajmg.b.20005.
6
Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.多巴胺转运体基因座上三个多态性的单倍型研究证实与注意力缺陷多动障碍存在连锁关系。
Biol Psychiatry. 2001 Feb 15;49(4):333-9. doi: 10.1016/s0006-3223(00)01053-2.
7
Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder.一种与注意力缺陷多动障碍相关的新型多巴胺β羟化酶基因变异体的鉴定及功能表征
World J Biol Psychiatry. 2015;16(8):610-8. doi: 10.3109/15622975.2015.1036771. Epub 2015 May 15.
8
[Association between dopamine beta hydroxylase gene and attention deficit hyperactivity disorder complicated with disruptive behavior disorder].多巴胺β羟化酶基因与注意缺陷多动障碍合并破坏性行为障碍之间的关联
Zhonghua Er Ke Za Zhi. 2005 Jan;43(1):26-30.
9
Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children.注意缺陷多动障碍儿童中多巴胺-β-羟化酶的多态性及低血浆活性
Neuro Endocrinol Lett. 2006 Dec;27(6):748-54.
10
Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder.注意缺陷多动障碍患者视觉注意力的时间分辨率受损与多巴胺β羟化酶基因型的关系
Biol Psychiatry. 2006 Nov 15;60(10):1039-45. doi: 10.1016/j.biopsych.2006.03.062. Epub 2006 Jul 28.

引用本文的文献

1
Catecholaminergic and cholinergic neuromodulation in autism spectrum disorder: A comparison to attention-deficit hyperactivity disorder.自闭症谱系障碍中的儿茶酚胺能和胆碱能神经调节:与注意力缺陷多动障碍的比较。
Front Neurosci. 2023 Jan 6;16:1078586. doi: 10.3389/fnins.2022.1078586. eCollection 2022.
2
Developmental Changes of Catecholamine-mediating Enzyme - Dopamine-β- Hydroxylase and Its Cofactors in Central and Peripheral Tissues and Serum of Long-Evans Rats.长 Evans 大鼠中枢和外周组织及血清中儿茶酚胺介导酶——多巴胺-β-羟化酶及其辅因子的发育变化
Int J Biomed Sci. 2012 Sep;8(3):194-203.
3
Molecular genetics of attention deficit hyperactivity disorder.
注意缺陷多动障碍的分子遗传学。
Psychiatr Clin North Am. 2010 Mar;33(1):159-80. doi: 10.1016/j.psc.2009.12.004.
4
Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India.东印度注意缺陷多动障碍患者的 DBH 基因多态性与血浆活性研究。
Cell Mol Neurobiol. 2010 Mar;30(2):265-74. doi: 10.1007/s10571-009-9448-5. Epub 2009 Sep 16.
5
Candidate gene studies of ADHD: a meta-analytic review.注意力缺陷多动障碍的候选基因研究:一项荟萃分析综述
Hum Genet. 2009 Jul;126(1):51-90. doi: 10.1007/s00439-009-0694-x. Epub 2009 Jun 9.
6
Genetic aspects in attention-deficit/hyperactivity disorder.注意缺陷多动障碍的遗传学方面
J Neural Transm (Vienna). 2008;115(2):305-15. doi: 10.1007/s00702-007-0839-9. Epub 2008 Jan 16.
7
Novel repeat polymorphisms of the dopaminergic neurotransmitter genes among dogs and wolves.犬类和狼类中多巴胺能神经递质基因的新型重复多态性
Mamm Genome. 2007 Dec;18(12):871-9. doi: 10.1007/s00335-007-9070-0. Epub 2007 Nov 30.
8
Family-based versus unrelated case-control designs for genetic associations.用于基因关联研究的基于家系与非亲缘病例对照设计
PLoS Genet. 2006 Aug;2(8):e123. doi: 10.1371/journal.pgen.0020123. Epub 2006 Jun 26.
9
An examination of the behavioral and neuropsychological correlates of three ADHD candidate gene polymorphisms (DRD4 7+, DBH TaqI A2, and DAT1 40 bp VNTR) in hyperactive and normal children followed to adulthood.对多动儿童和正常儿童的三种注意力缺陷多动障碍候选基因多态性(DRD4 7+、DBH TaqI A2和DAT1 40 bp VNTR)的行为和神经心理学相关性进行了研究,这些儿童随访至成年。
Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 5;141B(5):487-98. doi: 10.1002/ajmg.b.30326.
10
Brief report: pervasive developmental disorder can evolve into ADHD: case illustrations.简短报告:广泛性发育障碍可演变为注意力缺陷多动障碍:病例说明
J Autism Dev Disord. 2005 Aug;35(4):525-34. doi: 10.1007/s10803-005-5066-3.