• 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

注意缺陷多动障碍症状的神经机制存在 MAOA 基因型分层。

Neural mechanisms of attention-deficit/hyperactivity disorder symptoms are stratified by MAOA genotype.

机构信息

Medical Research Council-Social, Genetic and Developmental Psychiatry Centre (CN, TJ, SL, BR, SD, GB, AC, PC, EL, GS), Institute of Psychiatry, King's College London, London, United Kingdom.

出版信息

Biol Psychiatry. 2013 Oct 15;74(8):607-14. doi: 10.1016/j.biopsych.2013.03.027. Epub 2013 Jun 5.

DOI:10.1016/j.biopsych.2013.03.027
PMID:23746540
Abstract

BACKGROUND

Attention-deficit/hyperactivity disorder (ADHD) is characterized by deficits in reward sensitivity and response inhibition. The relative contribution of these frontostriatal mechanisms to ADHD symptoms and their genetic determinants is largely unexplored.

METHODS

Using functional magnetic resonance imaging and genetic analysis of the monoamine oxidase A (MAOA) gene, we investigated how striatal and inferior frontal activation patterns contribute to ADHD symptoms depending on MAOA genotype in a sample of adolescent boys (n = 190).

RESULTS

We demonstrate an association of ADHD symptoms with distinct blood oxygen level-dependent (BOLD) responses depending on MAOA genotype. In A hemizygotes of the expression single nucleotide polymorphism rs12843268, which express lower levels of MAOA, ADHD symptoms are associated with lower ventral striatal BOLD response during the monetary incentive delay task and lower inferior frontal gyrus BOLD response during the stop signal task. In G hemizygotes, ADHD symptoms are associated with increased inferior frontal gyrus BOLD response during the stop signal task in the presence of increased ventral striatal BOLD response during the monetary incentive delay task.

CONCLUSIONS

Depending on MAOA genotype, ADHD symptoms in adolescent boys are associated with either reward deficiency or insufficient response inhibition. Apart from its mechanistic interest, our finding may aid in developing pharmacogenetic markers for ADHD.

摘要

背景

注意力缺陷多动障碍(ADHD)的特征是奖赏敏感性和反应抑制缺陷。这些额-纹状体机制对 ADHD 症状及其遗传决定因素的相对贡献在很大程度上尚未得到探索。

方法

我们使用功能磁共振成像和单胺氧化酶 A(MAOA)基因的遗传分析,在一组青少年男孩(n = 190)中,根据 MAOA 基因型,研究了纹状体和额下回的激活模式如何根据 MAOA 基因型对 ADHD 症状产生影响。

结果

我们证明了 ADHD 症状与 MAOA 基因型相关的不同血氧水平依赖(BOLD)反应有关。在表达单核苷酸多态性 rs12843268 的 A 半合子中,MAOA 表达水平较低,ADHD 症状与金钱奖励延迟任务期间腹侧纹状体 BOLD 反应降低以及停止信号任务期间额下回 BOLD 反应降低有关。在 G 半合子中,ADHD 症状与停止信号任务期间额下回 BOLD 反应增加有关,同时在金钱奖励延迟任务期间腹侧纹状体 BOLD 反应增加。

结论

在青少年男孩中,ADHD 症状与 MAOA 基因型有关,要么与奖赏缺乏有关,要么与反应抑制不足有关。除了其机制上的兴趣外,我们的发现可能有助于开发 ADHD 的药物遗传学标志物。

相似文献

1
Neural mechanisms of attention-deficit/hyperactivity disorder symptoms are stratified by MAOA genotype.注意缺陷多动障碍症状的神经机制存在 MAOA 基因型分层。
Biol Psychiatry. 2013 Oct 15;74(8):607-14. doi: 10.1016/j.biopsych.2013.03.027. Epub 2013 Jun 5.
2
The Altered Brain Activation of Phonological Working Memory, Dual Tasking, and Distraction Among Participants With Adult ADHD and the Effect of the MAOA Polymorphism.成年 ADHD 患者在语音工作记忆、双重任务和分心时大脑激活的改变,以及 MAOA 多态性的影响。
J Atten Disord. 2018 Feb;22(3):240-249. doi: 10.1177/1087054715572609. Epub 2015 Mar 16.
3
Striatal sensitivity during reward processing in attention-deficit/hyperactivity disorder.纹状体在注意缺陷多动障碍的奖励处理过程中的敏感性。
J Am Acad Child Adolesc Psychiatry. 2012 Jul;51(7):722-732.e9. doi: 10.1016/j.jaac.2012.05.006. Epub 2012 Jun 5.
4
Differential association between MAOA, ADHD and neuropsychological functioning in boys and girls.男孩和女孩中MAOA、注意力缺陷多动障碍(ADHD)与神经心理功能之间的差异关联。
Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1524-30. doi: 10.1002/ajmg.b.30845.
5
Association of Monoamine Oxidase A (MAOA) Gene uVNTR and rs6323 Polymorphisms with Attention Deficit and Hyperactivity Disorder in Korean Children.单胺氧化酶 A(MAOA)基因 uVNTR 和 rs6323 多态性与韩国儿童注意缺陷多动障碍的关联。
Medicina (Kaunas). 2018 May 18;54(3):32. doi: 10.3390/medicina54030032.
6
Response inhibition and reward anticipation in medication-naïve adults with attention-deficit/hyperactivity disorder: a within-subject case-control neuroimaging study.药物初治注意缺陷多动障碍成年患者的反应抑制和奖励预期:一项基于个体的病例对照神经影像学研究。
Hum Brain Mapp. 2012 Oct;33(10):2350-61. doi: 10.1002/hbm.21368. Epub 2011 Aug 8.
7
Impact of a Common Genetic Variation Associated With Putamen Volume on Neural Mechanisms of Attention-Deficit/Hyperactivity Disorder.与壳核体积相关的常见遗传变异对注意缺陷多动障碍神经机制的影响。
J Am Acad Child Adolesc Psychiatry. 2017 May;56(5):436-444.e4. doi: 10.1016/j.jaac.2017.02.009. Epub 2017 Mar 8.
8
Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity.中国汉族注意缺陷多动障碍患者 MAOA 基因的关联分析:基于家系的关联检验、病例对照研究和冲动性的定量特征。
Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):737-48. doi: 10.1002/ajmg.b.31217. Epub 2011 Jul 14.
9
MAOA is associated with methylphenidate improvement of oppositional symptoms in boys with attention deficit hyperactivity disorder.MAOA 与哌醋甲酯改善注意缺陷多动障碍男孩的对立症状有关。
Int J Neuropsychopharmacol. 2009 Jun;12(5):709-14. doi: 10.1017/S1461145709000212. Epub 2009 Mar 24.
10
Gene-gene interaction between COMT and MAOA potentially predicts the intelligence of attention-deficit hyperactivity disorder boys in China.COMT 和 MAOA 基因之间的相互作用可能预测中国注意缺陷多动障碍男孩的智力。
Behav Genet. 2010 May;40(3):357-65. doi: 10.1007/s10519-009-9314-8. Epub 2009 Nov 26.

引用本文的文献

1
Interference of default mode on attention networks in adults with attention-deficit/hyperactivity disorder and its association with genetic variants and treatment outcomes.注意缺陷多动障碍患者注意网络中默认模式的干扰及其与遗传变异和治疗效果的关系。
CNS Neurosci Ther. 2024 Aug;30(8):e14900. doi: 10.1111/cns.14900.
2
Modeling genotype-protein interaction and correlation for Alzheimer's disease: a multi-omics imaging genetics study.阿尔茨海默病的基因型-蛋白相互作用和相关性建模:一项多组学影像遗传学研究。
Brief Bioinform. 2024 Jan 22;25(2). doi: 10.1093/bib/bbae038.
3
Genetic Variant and Major Depressive Disorder: A Systematic Review.
遗传变异与重度抑郁症:系统评价。
Cells. 2022 Oct 17;11(20):3267. doi: 10.3390/cells11203267.
4
Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder.遗传变异影响注意缺陷多动障碍患者的大脑变化。
Transl Psychiatry. 2021 Jun 5;11(1):349. doi: 10.1038/s41398-021-01473-w.
5
Monoamine Oxidase A is a Major Mediator of Mitochondrial Homeostasis and Glycolysis in Gastric Cancer Progression.单胺氧化酶A是胃癌进展中线粒体稳态和糖酵解的主要调节因子。
Cancer Manag Res. 2020 Sep 4;12:8023-8035. doi: 10.2147/CMAR.S257848. eCollection 2020.
6
The IMAGEN study: a decade of imaging genetics in adolescents.IMAGEN 研究:青少年影像遗传学十年。
Mol Psychiatry. 2020 Nov;25(11):2648-2671. doi: 10.1038/s41380-020-0822-5. Epub 2020 Jun 29.
7
The role of monoamine oxidase A in the neurobiology of aggressive, antisocial, and violent behavior: A tale of mice and men.单胺氧化酶 A 在攻击性行为、反社会行为和暴力行为的神经生物学中的作用:一个关于老鼠和人类的故事。
Prog Neurobiol. 2020 Nov;194:101875. doi: 10.1016/j.pneurobio.2020.101875. Epub 2020 Jun 20.
8
Neurobehavioural characterisation and stratification of reinforcement-related behaviour.神经行为特征与强化相关行为的分层。
Nat Hum Behav. 2020 May;4(5):544-558. doi: 10.1038/s41562-020-0846-5. Epub 2020 Apr 20.
9
Disrupted brain functional networks in drug-naïve children with attention deficit hyperactivity disorder assessed using graph theory analysis.采用图论分析评估未经药物治疗的注意缺陷多动障碍儿童的大脑功能网络紊乱。
Hum Brain Mapp. 2019 Dec 1;40(17):4877-4887. doi: 10.1002/hbm.24743. Epub 2019 Jul 30.
10
Reward Processing in Drug-Naive Youth with Various Levels of Risk for Substance Use Disorders: A Pilot Study.不同物质使用障碍风险水平的未使用药物青少年的奖赏处理:一项初步研究。
J Child Adolesc Psychopharmacol. 2019 Aug;29(7):516-525. doi: 10.1089/cap.2018.0175. Epub 2019 Jun 10.