• 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

两个多巴胺基因与童年期回顾性注意力不集中和品行障碍症状的报告相关。

Two dopamine genes related to reports of childhood retrospective inattention and conduct disorder symptoms.

作者信息

Rowe D C, Stever C, Chase D, Sherman S, Abramowitz A, Waldman I D

机构信息

Graduate Committee in Genetics and Division of Family Studies and Human Development, Campus Box 210033, University of Arizona, Tucson, AZ 85721, USA.

出版信息

Mol Psychiatry. 2001 Jul;6(4):429-33. doi: 10.1038/sj.mp.4000874.

DOI:10.1038/sj.mp.4000874
PMID:11443528
Abstract

The 7-repeat allele of the dopamine receptor D4 gene (DRD4) and the 10 repeat allele of the dopamine transporter gene (DAT1) have shown association and linkage with symptoms of attention deficit hyperactivity disorder (ADHD) in childhood. The parents of ADHD children (clinic group, n = 80 fathers and 107 mothers) and control children (control group, n = 42 fathers and 51 mothers) were the focus of this study. These parents reported retrospectively on their level of ADHD Inattention and Conduct Disorder symptoms in adolescence. In analyses of the relation of symptom levels to the DRD4 and DAT1 genotypes, fathers possessing the 7 repeat DRD4 allele had greater levels of both inattention and conduct disorder symptoms. Mothers with the 10/10 genotype had higher levels of inattention symptoms. Thus, genetic associations found in children may be replicable in their parents.

摘要

多巴胺受体D4基因(DRD4)的7重复等位基因和多巴胺转运体基因(DAT1)的10重复等位基因已显示出与儿童注意力缺陷多动障碍(ADHD)症状的关联和连锁关系。本研究的重点是ADHD儿童的父母(临床组,80名父亲和107名母亲)和对照儿童的父母(对照组,42名父亲和51名母亲)。这些父母回顾性报告了他们在青少年时期ADHD注意力不集中和品行障碍症状的水平。在分析症状水平与DRD4和DAT1基因型的关系时,拥有7重复DRD4等位基因的父亲在注意力不集中和品行障碍症状方面的水平更高。具有10/10基因型的母亲注意力不集中症状水平更高。因此,在儿童中发现的基因关联可能在其父母中得到复制。

相似文献

1
Two dopamine genes related to reports of childhood retrospective inattention and conduct disorder symptoms.两个多巴胺基因与童年期回顾性注意力不集中和品行障碍症状的报告相关。
Mol Psychiatry. 2001 Jul;6(4):429-33. doi: 10.1038/sj.mp.4000874.
2
Transmission disequilibrium testing of dopamine-related candidate gene polymorphisms in ADHD: confirmation of association of ADHD with DRD4 and DRD5.注意缺陷多动障碍中多巴胺相关候选基因多态性的传递不平衡检验:注意缺陷多动障碍与多巴胺受体D4和多巴胺受体D5关联的确认
Mol Psychiatry. 2004 Jul;9(7):711-7. doi: 10.1038/sj.mp.4001466.
3
Genetic interaction analysis for DRD4 and DAT1 genes in a group of Mexican ADHD patients.一组墨西哥多动症患者中DRD4和DAT1基因的遗传相互作用分析。
Neurosci Lett. 2009 Feb 27;451(3):257-60. doi: 10.1016/j.neulet.2009.01.004. Epub 2009 Jan 8.
4
Dopamine risk and paternal ADHD symptomatology associated with ADHD symptoms in four and a half-year-old boys.多巴胺风险及父亲的多动症症状与四岁半男孩的多动症症状相关。
Psychiatr Genet. 2010 Aug;20(4):160-5. doi: 10.1097/YPG.0b013e32833a1f27.
5
[Distribution of DRD4 and DAT1 alleles from dopaminergic system in a mixed Chilean population].[智利混合人群中多巴胺能系统DRD4和DAT1等位基因的分布]
Rev Med Chil. 2003 Feb;131(2):135-43.
6
Family-based association study between bipolar disorder and DRD2, DRD4, DAT, and SERT in Sardinia.撒丁岛双相情感障碍与多巴胺受体D2、多巴胺受体D4、多巴胺转运体和5-羟色胺转运体的家系关联研究。
Am J Med Genet. 1999 Oct 15;88(5):522-6.
7
A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder.一项关于注意力缺陷多动障碍中多巴胺D4受体基因和多巴胺转运体基因的基于家系和病例对照的关联研究。
Mol Psychiatry. 2000 Sep;5(5):523-30. doi: 10.1038/sj.mp.4000751.
8
[Combination of DRD4 and DAT1 genotypes is an important risk factor for attention deficit disorder with hyperactivity families living in Santiago, Chile].[DRD4和DAT1基因组合是智利圣地亚哥患有多动症的注意力缺陷障碍家庭的重要风险因素]
Rev Med Chil. 2008 Jun;136(6):719-24. Epub 2008 Aug 26.
9
The dopamine transporter gene and the impulsivity phenotype in attention deficit hyperactivity disorder: a case-control association study in a Korean sample.注意力缺陷多动障碍中的多巴胺转运体基因与冲动性表型:韩国样本中的病例对照关联研究
J Psychiatr Res. 2006 Dec;40(8):730-7. doi: 10.1016/j.jpsychires.2005.11.002. Epub 2005 Dec 20.
10
Double dissociation between lab measures of inattention and impulsivity and the dopamine transporter gene (DAT1) and dopamine D4 receptor gene (DRD4).注意缺陷多动障碍的实验室测量与多巴胺转运体基因(DAT1)和多巴胺 D4 受体基因(DRD4)之间的双重分离。
J Abnorm Psychol. 2012 Nov;121(4):1011-23. doi: 10.1037/a0028225. Epub 2012 May 7.

引用本文的文献

1
Adult attention deficit hyperactivity disorder symptom profiles and concurrent problems with alcohol and cannabis: sex differences in a representative, population survey.成人注意力缺陷多动障碍症状特征以及与酒精和大麻相关的并发问题:一项具有代表性的人群调查中的性别差异
BMC Psychiatry. 2016 Feb 27;16:50. doi: 10.1186/s12888-016-0746-4.
2
Structure and etiology of co-occurring internalizing and externalizing disorders in adolescents.青少年共病的内化和外化障碍的结构和病因。
J Abnorm Child Psychol. 2011 Jan;39(1):109-23. doi: 10.1007/s10802-010-9444-8.
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
Catechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHD.儿茶酚氧位甲基转移酶(COMT)Val108/158 Met基因多态性不会调节多动症儿童的执行功能。
BMC Med Genet. 2004 Dec 21;5:30. doi: 10.1186/1471-2350-5-30.
5
A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men.烟碱型乙酰胆碱受体α4亚基基因的一种常见单倍型与男性对尼古丁成瘾的易感性相关。
Am J Hum Genet. 2004 Jul;75(1):112-21. doi: 10.1086/422194. Epub 2004 May 20.
6
A drosophila model for attention deficit hyperactivity disorder (ADHD): No evidence of association with PRKG1 gene.一种注意力缺陷多动障碍(ADHD)的果蝇模型:无证据表明与PRKG1基因有关联。
Neuromolecular Med. 2002;2(3):281-7. doi: 10.1385/NMM:2:3:281.