• 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

缬氨酸158蛋氨酸多态性与社会功能损害交互影响健康青少年的注意力缺陷多动症状。

Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents.

作者信息

Millenet Sabina K, Nees Frauke, Heintz Stefan, Bach Christiane, Frank Josef, Vollstädt-Klein Sabine, Bokde Arun, Bromberg Uli, Büchel Christian, Quinlan Erin B, Desrivières Sylvane, Fröhner Juliane, Flor Herta, Frouin Vincent, Garavan Hugh, Gowland Penny, Heinz Andreas, Ittermann Bernd, Lemaire Herve, Martinot Jean-Luc, Martinot Marie-Laure P, Papadoulos Dimitri O, Paus Tomáš, Poustka Luise, Rietschel Marcella, Smolka Michael N, Walter Henrik, Whelan Rob, Schumann Gunter, Banaschewski Tobias, Hohmann Sarah

机构信息

Department of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Department of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

出版信息

Front Genet. 2018 Jul 31;9:284. doi: 10.3389/fgene.2018.00284. eCollection 2018.

DOI:10.3389/fgene.2018.00284
PMID:30108607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6079264/
Abstract

The dopaminergic system has been shown to have substantial effects on the etiology of attention-deficit hyperactivity disorder (ADHD). However, while some studies found a significant direct effect, others did not. In this context, social behavior might play an important role as a factor that is related both to the dopaminergic system and ADHD. In a large epidemiological sample of adolescents ( = 462; 16-17 years), we assessed the level of ADHD symptoms using the Strengths and Difficulties Questionnaire, social behavior using the Social Responsiveness Scale, and the allelic distribution of the dopaminergic catechol--methyltransferase () Val158Met polymorphism. We found a significant association between and social impairment, insofar as Met-allele carriers showed increased levels of social impairment. Moreover, social impairment significantly determined an association between and ADHD (explained variance: 19.09%). This effect did not significantly differ between males and females. and social impairment might interactively affect ADHD symptomatology, and could thus represent significant gene-phenotypic risk factors for ADHD symptomatology. This might have interesting implications for prevention and intervention strategies with a focus on social behavior in genetically at-risk individuals.

摘要

多巴胺能系统已被证明对注意力缺陷多动障碍(ADHD)的病因有重大影响。然而,虽然一些研究发现了显著的直接影响,但其他研究则未发现。在这种情况下,社会行为可能作为一个与多巴胺能系统和ADHD都相关的因素发挥重要作用。在一个大型青少年流行病学样本(n = 462;16 - 17岁)中,我们使用优势与困难问卷评估ADHD症状水平,使用社会反应量表评估社会行为,并评估多巴胺能儿茶酚 - O - 甲基转移酶(COMT)Val158Met多态性的等位基因分布。我们发现COMT与社会功能损害之间存在显著关联,因为携带Met等位基因者的社会功能损害水平有所增加。此外,社会功能损害显著决定了COMT与ADHD之间的关联(解释方差:19.09%)。这种效应在男性和女性之间没有显著差异。COMT和社会功能损害可能相互作用影响ADHD症状表现,因此可能是ADHD症状表现的重要基因 - 表型风险因素。这可能对以遗传易患个体的社会行为为重点的预防和干预策略具有有趣的启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7799/6079264/2950777e1d06/fgene-09-00284-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7799/6079264/164f807631ab/fgene-09-00284-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7799/6079264/2950777e1d06/fgene-09-00284-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7799/6079264/164f807631ab/fgene-09-00284-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7799/6079264/2950777e1d06/fgene-09-00284-g002.jpg

相似文献

1
Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents.缬氨酸158蛋氨酸多态性与社会功能损害交互影响健康青少年的注意力缺陷多动症状。
Front Genet. 2018 Jul 31;9:284. doi: 10.3389/fgene.2018.00284. eCollection 2018.
2
Catechol--methyltransferase Genotype and Early-Life Family Adversity Interactively Affect Attention-Deficit Hyperactivity Symptoms Across Childhood.儿茶酚 - 甲基转移酶基因型与童年早期家庭逆境对儿童期注意缺陷多动症状产生交互影响。
Front Genet. 2020 Jul 10;11:724. doi: 10.3389/fgene.2020.00724. eCollection 2020.
3
The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.儿茶酚-O-甲基转移酶(COMT)基因多态性的甲硫氨酸等位基因会损害患有注意力缺陷多动障碍(ADHD)的儿童和青少年的前额叶认知功能。
Exp Brain Res. 2005 Jun;163(3):352-60. doi: 10.1007/s00221-004-2180-y. Epub 2005 Jan 15.
4
Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.儿茶酚-O-甲基转移酶(COMT)单倍型与成人多动症状严重程度之间的关联。
Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):403-10. doi: 10.1002/ajmg.b.30831.
5
No association between catechol-O-methyltransferase (COMT) genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children.日本儿童中儿茶酚-O-甲基转移酶(COMT)基因型与注意力缺陷多动障碍(ADHD)之间无关联。
Brain Dev. 2014 Aug;36(7):620-5. doi: 10.1016/j.braindev.2013.08.006. Epub 2013 Sep 12.
6
White matter alterations related to attention-deficit hyperactivity disorder and COMT val(158)met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus).与注意力缺陷多动障碍及儿茶酚-O-甲基转移酶(COMT)基因val(158)met多态性相关的白质改变:缬氨酸纯合子型注意力缺陷多动障碍儿童右侧扣带束(扣带回)的白质连接性发生改变。
Neuropsychiatr Dis Treat. 2016 Apr 21;12:969-81. doi: 10.2147/NDT.S104450. eCollection 2016.
7
[Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene].注意缺陷多动障碍与儿茶酚-O-甲基转移酶基因Val158Met多态性的关联分析
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):322-4.
8
A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD).一项基于家庭的儿茶酚-O-甲基转移酶(COMT)与注意力缺陷多动障碍(ADHD)的研究。
Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):64-7. doi: 10.1002/ajmg.b.30123.
9
Association of Val158Met polymorphism in COMT gene with attention-deficit hyperactive disorder: An updated meta-analysis.儿茶酚-O-甲基转移酶(COMT)基因Val158Met多态性与注意缺陷多动障碍的关联:一项更新的荟萃分析。
Medicine (Baltimore). 2020 Nov 25;99(48):e23400. doi: 10.1097/MD.0000000000023400.
10
Structural correlates of COMT Val158Met polymorphism in childhood ADHD: a voxel-based morphometry study.儿童注意力缺陷多动障碍中儿茶酚-O-甲基转移酶(COMT)基因Val158Met多态性的结构相关性:一项基于体素的形态学研究
World J Biol Psychiatry. 2015 Apr;16(3):190-9. doi: 10.3109/15622975.2014.984629. Epub 2014 Dec 15.

引用本文的文献

1
Environmental enrichment promotes adaptive responding during tests of behavioral regulation in male heterogeneous stock rats.环境丰容可促进雄性异质 stock 大鼠行为调节测试中的适应性反应。
Sci Rep. 2024 Feb 20;14(1):4182. doi: 10.1038/s41598-024-53943-y.
2
Pharmacodynamic Gene Testing in Prader-Willi Syndrome.普拉德-威利综合征的药效基因检测
Front Genet. 2020 Nov 20;11:579609. doi: 10.3389/fgene.2020.579609. eCollection 2020.
3
Catechol--methyltransferase Genotype and Early-Life Family Adversity Interactively Affect Attention-Deficit Hyperactivity Symptoms Across Childhood.

本文引用的文献

1
Association between COMT Val158Met and psychiatric disorders: A comprehensive meta-analysis.儿茶酚-O-甲基转移酶(COMT)基因Val158Met与精神疾病的关联:一项综合荟萃分析。
Am J Med Genet B Neuropsychiatr Genet. 2018 Mar;177(2):199-210. doi: 10.1002/ajmg.b.32556. Epub 2017 Jun 13.
2
The Emerging Neuroscience of Intrinsic Motivation: A New Frontier in Self-Determination Research.内在动机的新兴神经科学:自我决定研究的新前沿。
Front Hum Neurosci. 2017 Mar 24;11:145. doi: 10.3389/fnhum.2017.00145. eCollection 2017.
3
Adolescent externalizing behaviour, psychological control, and peer rejection: Transactional links and dopaminergic moderation.
儿茶酚 - 甲基转移酶基因型与童年早期家庭逆境对儿童期注意缺陷多动症状产生交互影响。
Front Genet. 2020 Jul 10;11:724. doi: 10.3389/fgene.2020.00724. eCollection 2020.
4
The effect of alcohol use on neuroimaging correlates of cognitive and emotional processing in human adolescence.酒精使用对人类青少年认知和情感处理的神经影像学相关性的影响。
Neuropsychology. 2019 Sep;33(6):781-794. doi: 10.1037/neu0000555.
青少年外化行为、心理控制与同伴排斥:相互作用的关系及多巴胺能的调节作用
Br J Dev Psychol. 2017 Sep;35(3):420-438. doi: 10.1111/bjdp.12184. Epub 2017 Mar 24.
4
Social Functioning in Children With or At Risk for Attention Deficit/Hyperactivity Disorder: A Meta-Analytic Review.注意缺陷多动障碍患儿或有患病风险儿童的社会功能:一项荟萃分析综述。
J Clin Child Adolesc Psychol. 2018 Mar-Apr;47(2):213-235. doi: 10.1080/15374416.2016.1266644. Epub 2017 Jan 27.
5
Hierarchical prediction errors in midbrain and septum during social learning.社交学习过程中中脑和隔膜的分层预测误差
Soc Cogn Affect Neurosci. 2017 Apr 1;12(4):618-634. doi: 10.1093/scan/nsw171.
6
Effect of trait anxiety on cognitive test performance in adolescents with and without attention-deficit/hyperactivity disorder.特质焦虑对患有和未患有注意力缺陷/多动障碍青少年认知测试表现的影响。
J Clin Exp Neuropsychol. 2017 Jun;39(5):434-448. doi: 10.1080/13803395.2016.1232373. Epub 2016 Oct 3.
7
Evidence for increased behavioral control by punishment in children with attention-deficit hyperactivity disorder.注意缺陷多动障碍儿童中惩罚增强行为控制的证据。
J Child Psychol Psychiatry. 2017 Mar;58(3):248-257. doi: 10.1111/jcpp.12635. Epub 2016 Sep 9.
8
Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.成人注意力缺陷多动障碍:一项关于遗传、药物遗传学和生化研究的系统评价与荟萃分析。
Mol Psychiatry. 2016 Jul;21(7):872-84. doi: 10.1038/mp.2016.74. Epub 2016 May 24.
9
Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention.自闭症高风险兄弟姐妹中的多巴胺能变异:与发起共同注意的关联。
Autism Res. 2016 Nov;9(11):1142-1150. doi: 10.1002/aur.1623. Epub 2016 Mar 15.
10
Genetics of attention-deficit/hyperactivity disorder: an update.注意力缺陷多动障碍的遗传学:最新进展
Expert Rev Neurother. 2016;16(2):145-56. doi: 10.1586/14737175.2016.1130626. Epub 2016 Jan 11.