• 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

儿茶酚-O-甲基转移酶(COMT)基因Val108/158Met变异、出生体重与注意缺陷多动障碍(ADHD)儿童的品行障碍

COMT Val108/158Met gene variant, birth weight, and conduct disorder in children with ADHD.

作者信息

Sengupta Sarojini M, Grizenko Natalie, Schmitz Norbert, Schwartz George, Ben Amor Leila, Bellingham Johanne, DE Guzman Rosherrie, Polotskaia Anna, Ter Stepanian Marina, Thakur Geeta, Joober Ridha

机构信息

Drs. Sengupta, Ben Amor, and Joober are with the Department of Human Genetics, Drs. Grizenko and Joober and Mr. Schwartz are with the Department of Psychiatry, Dr. Joober and Ms. Thakur are with the Department of Neurology and Neurosurgery, McGill University; and Drs. Sengupta, Schmitz, and Joober, Mr. Schwartz, Ms. Bellingham, Ms. de Guzman, Ms. Polotskaia, and Ms. Ter Stepanian are with Douglas Hospital Research Centre, Montreal, Quebec, Canada.

Drs. Sengupta, Ben Amor, and Joober are with the Department of Human Genetics, Drs. Grizenko and Joober and Mr. Schwartz are with the Department of Psychiatry, Dr. Joober and Ms. Thakur are with the Department of Neurology and Neurosurgery, McGill University; and Drs. Sengupta, Schmitz, and Joober, Mr. Schwartz, Ms. Bellingham, Ms. de Guzman, Ms. Polotskaia, and Ms. Ter Stepanian are with Douglas Hospital Research Centre, Montreal, Quebec, Canada..

出版信息

J Am Acad Child Adolesc Psychiatry. 2006 Nov;45(11):1363-1369. doi: 10.1097/01.chi.0000251212.44491.46.

DOI:10.1097/01.chi.0000251212.44491.46
PMID:17075359
Abstract

OBJECTIVE

In a recent study, Thapar and colleagues reported that COMT "gene variant and birth weight predict early-onset antisocial behavior in children" with attention-deficit/hyperactivity disorder. We have attempted to replicate these findings in a group of ADHD children using a similar research design.

METHOD

Children (n=191) between 6 and 12 years of age who were diagnosed with ADHD were included in the study. Conduct disorder was diagnosed according to DSM-IV criteria based on clinical evaluation and a structured interview (Diagnostic Interview Schedule for Children-IV). The mother's report on the child's birth weight was used in the analysis. Logistic regression analysis, with genotype and birth weight as independent variables and DSM-IV conduct disorder as the dependent variable, was conducted.

RESULTS

No significant main effects of genotype and birth weight or interaction effects on conduct disorder were observed.

CONCLUSION

In this sample of children diagnosed with ADHD, we find no association between the COMT ValMet gene variant, birth weight, and conduct disorder. Further investigations are required before using birth weight and COMT genotype as predictors of conduct disorder in children with attention-deficit/hyperactivity disorder, especially given the societal and legal ramifications of conduct disorder.

摘要

目的

在最近的一项研究中,萨帕尔及其同事报告称,儿茶酚-O-甲基转移酶(COMT)“基因变异和出生体重可预测患有注意力缺陷多动障碍(ADHD)儿童的早发性反社会行为”。我们试图采用类似的研究设计,在一组ADHD儿童中复制这些研究结果。

方法

本研究纳入了191名年龄在6至12岁之间、被诊断患有ADHD的儿童。根据《精神疾病诊断与统计手册》第四版(DSM-IV)标准,通过临床评估和结构化访谈(儿童诊断访谈量表第四版)对品行障碍进行诊断。分析中采用母亲报告的孩子出生体重。以基因型和出生体重作为自变量,以DSM-IV品行障碍作为因变量,进行了逻辑回归分析。

结果

未观察到基因型和出生体重的显著主效应,也未观察到它们对品行障碍的交互效应。

结论

在这个被诊断患有ADHD的儿童样本中,我们发现COMT ValMet基因变异、出生体重与品行障碍之间没有关联。在将出生体重和COMT基因型用作注意力缺陷多动障碍儿童品行障碍的预测指标之前,还需要进一步研究,尤其是考虑到品行障碍的社会和法律影响。

相似文献

1
COMT Val108/158Met gene variant, birth weight, and conduct disorder in children with ADHD.儿茶酚-O-甲基转移酶(COMT)基因Val108/158Met变异、出生体重与注意缺陷多动障碍(ADHD)儿童的品行障碍
J Am Acad Child Adolesc Psychiatry. 2006 Nov;45(11):1363-1369. doi: 10.1097/01.chi.0000251212.44491.46.
2
Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder.儿茶酚-O-甲基转移酶基因变异与出生体重可预测注意力缺陷多动障碍儿童的早发性反社会行为。
Arch Gen Psychiatry. 2005 Nov;62(11):1275-8. doi: 10.1001/archpsyc.62.11.1275.
3
Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.青少年男性违法者中,儿茶酚-O-甲基转移酶Val 158 Met多态性的变异与品行障碍和多动症症状相关。
Psychiatr Genet. 2010 Feb;20(1):20-4. doi: 10.1097/YPG.0b013e32833511e4.
4
Genotype link with extreme antisocial behavior: the contribution of cognitive pathways.基因型与极端反社会行为的关联:认知途径的作用
Arch Gen Psychiatry. 2010 Dec;67(12):1317-23. doi: 10.1001/archgenpsychiatry.2010.163.
5
A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder.注意缺陷多动障碍儿童反社会行为亚型的复制分子遗传基础。
Arch Gen Psychiatry. 2008 Feb;65(2):203-10. doi: 10.1001/archgenpsychiatry.2007.24.
6
Study of the catechol-o-methyltransferase (COMT) gene with high aggression in children.研究具有高攻击性的儿童的儿茶酚氧位甲基转移酶(COMT)基因。
Aggress Behav. 2013 Jan;39(1):45-51. doi: 10.1002/ab.21448. Epub 2012 Sep 12.
7
Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant.注意缺陷多动障碍表型受儿茶酚-O-甲基转移酶功能变体的影响。
J Neural Transm (Vienna). 2010 Feb;117(2):259-67. doi: 10.1007/s00702-009-0338-2. Epub 2009 Nov 28.
8
Genetic risk for conduct disorder symptom subtypes in an ADHD sample: specificity to aggressive symptoms.注意缺陷多动障碍样本中品行障碍症状亚型的遗传风险:对攻击性行为症状的特异性
J Am Acad Child Adolesc Psychiatry. 2009 Jul;48(7):757-764. doi: 10.1097/CHI.0b013e3181a5661b.
9
Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype.儿茶酚-O-甲基转移酶(COMT)与注意力缺陷多动障碍(ADHD)的单倍型相对风险研究:高酶活性Val等位基因与ADHD冲动多动表型的关联。
Am J Med Genet. 1999 Oct 15;88(5):497-502.
10
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.

引用本文的文献

1
Val/Met and Psychopathic Traits in Children and Adolescents: A Systematic Review and New Evidence of a Developmental Trajectory toward Psychopathy.Val/Met 与儿童和青少年的精神病态特征:系统综述及向精神病态发展轨迹的新证据。
Int J Mol Sci. 2022 Feb 4;23(3):1782. doi: 10.3390/ijms23031782.
2
Facing the Methodological Challenge in Dissecting the Genetics of ADHD: A Case for Deep Phenotyping and Heterogeneity Reduction.剖析注意力缺陷多动障碍遗传学面临的方法学挑战:深度表型分析与减少异质性的实例
J Can Acad Child Adolesc Psychiatry. 2020 Aug;29(3):188-201. Epub 2020 Aug 1.
3
Differences in Sensitivity to Environment Depending on Catechol-O-Methyltransferase (COMT) Gene? A Meta-analysis of Child and Adolescent Gene-by-Environment Studies.
根据儿茶酚-O-甲基转移酶(COMT)基因的敏感性差异?儿童和青少年基因-环境研究的荟萃分析。
J Youth Adolesc. 2019 Apr;48(4):655-667. doi: 10.1007/s10964-019-01004-3. Epub 2019 Mar 4.
4
A Meta-Analysis of the Association Between Birth Weight and Attention Deficit Hyperactivity Disorder.出生体重与注意缺陷多动障碍相关性的荟萃分析
J Abnorm Child Psychol. 2018 Oct;46(7):1409-1426. doi: 10.1007/s10802-017-0371-9.
5
COMT and prenatal maternal smoking in associations with conduct problems and crime: the Pelotas 1993 birth cohort study.儿茶酚-O-甲基转移酶(COMT)与产前母亲吸烟与行为问题和犯罪的关联:佩洛塔斯 1993 年出生队列研究。
Sci Rep. 2016 Jul 18;6:29900. doi: 10.1038/srep29900.
6
The Role of the Catechol-o-Methyltransferase (COMT) GeneVal158Met in Aggressive Behavior, a Review of Genetic Studies.儿茶酚-O-甲基转移酶(COMT)基因Val158Met在攻击行为中的作用:遗传学研究综述
Curr Neuropharmacol. 2015;13(6):802-14. doi: 10.2174/1570159x13666150612225836.
7
The association between the catechol-O-methyltransferase Val108/158Met polymorphism and hyperactive-impulsive and inattentive symptoms in youth.儿茶酚-O-甲基转移酶Val108/158Met基因多态性与青少年多动冲动及注意力不集中症状之间的关联。
Psychopharmacology (Berl). 2013 Nov;230(1):69-76. doi: 10.1007/s00213-013-3138-1. Epub 2013 May 29.
8
What have we learnt about the causes of ADHD?我们对 ADHD 的病因有哪些了解?
J Child Psychol Psychiatry. 2013 Jan;54(1):3-16. doi: 10.1111/j.1469-7610.2012.02611.x. Epub 2012 Sep 11.
9
Association of ADAM10 and CAMK2A polymorphisms with conduct disorder: evidence from family-based studies.ADAM10 和 CAMK2A 多态性与品行障碍的关联:来自基于家系的研究证据。
J Abnorm Child Psychol. 2011 Aug;39(6):773-82. doi: 10.1007/s10802-011-9524-4.
10
Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes.COMT Val108/158Met 多态性与母亲产前吸烟的相互作用预测攻击性行为结果。
Biol Psychol. 2011 Apr;87(1):99-105. doi: 10.1016/j.biopsycho.2011.02.013. Epub 2011 Feb 26.