• 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-甲基转移酶基因与精神分裂症的关联及其法医学意义

[Association and its forensic significance between COMT gene and schizophrenia].

作者信息

Ding Chun-Li, Zhou Xue, Wang Bao-Jie, Ding Mei, Pang Hao

机构信息

Key Laboratory of Evidence Identification in Universities of Shandong, Shandong University of Political Science and Law, Jinan 250014, China.

出版信息

Fa Yi Xue Za Zhi. 2012 Aug;28(4):299-304.

PMID:23033671
Abstract

Catechol-O-methyltransferase (COMT) gene encodes catechol-O-methyltransferase, the variant of this gene may affect the expression and metabolic activity of COMT. As the result of the changes of the effective concentration of the catecholamine neurotransmitter in the central nervous system, central nervous system dysfunctions associated with schizophrenia. This review summarizes genetic polymorphism and diversity of COMT gene. It also elaborates the relation between SNP and haplotype of COMT gene and three aspects, which including schizophrenia, attacking and violent tendency, and the frontal cognitive function of the schizophreniac. The correlativity study between genetic variation of the COMT gene and schizophrenia in patients with attacking and violent tendency may be helpful for the assessment of forensic psychiatry.

摘要

儿茶酚-O-甲基转移酶(COMT)基因编码儿茶酚-O-甲基转移酶,该基因的变体可能会影响COMT的表达和代谢活性。由于中枢神经系统中儿茶酚胺神经递质有效浓度的变化,会出现与精神分裂症相关的中枢神经系统功能障碍。本综述总结了COMT基因的遗传多态性和多样性。还阐述了COMT基因的单核苷酸多态性(SNP)与单倍型之间的关系以及三个方面,包括精神分裂症、攻击和暴力倾向以及精神分裂症患者的额叶认知功能。对有攻击和暴力倾向患者的COMT基因遗传变异与精神分裂症之间的相关性研究可能有助于法医精神病学的评估。

相似文献

1
[Association and its forensic significance between COMT gene and schizophrenia].儿茶酚-O-甲基转移酶基因与精神分裂症的关联及其法医学意义
Fa Yi Xue Za Zhi. 2012 Aug;28(4):299-304.
2
A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val158Met genotype.儿茶酚-O-甲基转移酶(COMT)的一种新型蛋白质异构体:精神分裂症和双相情感障碍中的脑表达分析及Val158Met基因型的影响
Mol Psychiatry. 2006 Feb;11(2):116-7. doi: 10.1038/sj.mp.4001767.
3
COMT haplotypes suggest P2 promoter region relevance for schizophrenia.儿茶酚-O-甲基转移酶单倍型表明P2启动子区域与精神分裂症有关。
Mol Psychiatry. 2004 Sep;9(9):859-70. doi: 10.1038/sj.mp.4001496.
4
Relationship of catechol-O-methyltransferase to schizophrenia and its correlates: evidence for associations and complex interactions.儿茶酚-O-甲基转移酶与精神分裂症及其相关因素的关系:关联和复杂相互作用的证据
Harv Rev Psychiatry. 2007 Sep-Oct;15(5):233-44. doi: 10.1080/10673220701650409.
5
Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia.工作记忆中的执行子过程:与儿茶酚-O-甲基转移酶Val158Met基因型及精神分裂症的关系
Arch Gen Psychiatry. 2003 Sep;60(9):889-96. doi: 10.1001/archpsyc.60.9.889.
6
Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol O-methyltransferase (COMT) activity.精神分裂症中的杀人行为与一种决定儿茶酚氧位甲基转移酶(COMT)低活性的基因多态性有关。
Am J Med Genet. 1999 Dec 15;88(6):628-33.
7
Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.儿茶酚-O-甲基转移酶(COMT)和脯氨酸脱氢酶(PRODH)的基因变异与精神分裂症患者的脑解剖结构有关。
Genes Brain Behav. 2008 Feb;7(1):61-9. doi: 10.1111/j.1601-183X.2007.00326.x. Epub 2007 May 14.
8
Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families.儿茶酚-O-甲基转移酶(COMT)基因的变异与爱尔兰高密度家庭中的精神分裂症有关。
Mol Psychiatry. 2004 Oct;9(10):962-7. doi: 10.1038/sj.mp.4001519.
9
Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.精神分裂症、双相情感障碍和重度抑郁症患者背外侧前额叶皮质中的儿茶酚-O-甲基转移酶(COMT)和脯氨酸脱氢酶(PRODH)信使核糖核酸
Synapse. 2004 Feb;51(2):112-8. doi: 10.1002/syn.10286.
10
Association study of a functional catechol-O-methyltransferase genetic polymorphism with age of onset, cognitive function, symptomatology and prognosis in chronic schizophrenia.慢性精神分裂症中功能性儿茶酚-O-甲基转移酶基因多态性与发病年龄、认知功能、症状学及预后的关联研究
Neuropsychobiology. 2004;49(4):196-200. doi: 10.1159/000077366.