• 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

相似文献

1
No association between PAWR gene polymorphisms and tardive dyskinesia in schizophrenia patients.PAWR 基因多态性与精神分裂症患者迟发性运动障碍无关。
Psychiatry Investig. 2012 Jun;9(2):191-4. doi: 10.4306/pi.2012.9.2.191. Epub 2012 May 22.
2
No Evidence for an Association between Dopamine D2 Receptor Polymorphisms and Tardive Dyskinesia in Korean Schizophrenia Patients.在韩国精神分裂症患者中,没有多巴胺 D2 受体多态性与迟发性运动障碍之间关联的证据。
Psychiatry Investig. 2011 Mar;8(1):49-54. doi: 10.4306/pi.2011.8.1.49. Epub 2011 Mar 10.
3
No Evidence for Association between Tyrosine Hydroxylase Gene Val81Met Polymorphism and Susceptibility to Tardive Dyskinesia in Schizophrenia.没有证据表明酪氨酸羟化酶基因 Val81Met 多态性与精神分裂症迟发性运动障碍易感性有关。
Psychiatry Investig. 2009 Jun;6(2):108-11. doi: 10.4306/pi.2009.6.2.108. Epub 2009 Jun 30.
4
[Pharmacogenetic assessment of antipsychotic-induced tardive dyskinesia: contribution of 5-hydroxytryptamine 2C receptor gene and of a combination of dopamine D3 variant allele (Gly) and MnSOD wild allele (Val)].抗精神病药物所致迟发性运动障碍的药物遗传学评估:5-羟色胺2C受体基因以及多巴胺D3变异等位基因(甘氨酸)与锰超氧化物歧化酶野生等位基因(缬氨酸)组合的作用
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):98-102.
5
No association between dopamine D4 receptor gene -521 C/T polymorphism and tardive dyskinesia in schizophrenia.精神分裂症患者中多巴胺D4受体基因-521 C/T多态性与迟发性运动障碍之间无关联。
Neuropsychobiology. 2007;55(1):47-51. doi: 10.1159/000103576. Epub 2007 Jun 8.
6
No evidence for an association between G protein beta3 subunit gene C825T polymorphism and tardive dyskinesia in schizophrenia.无证据表明G蛋白β3亚基基因C825T多态性与精神分裂症迟发性运动障碍之间存在关联。
Hum Psychopharmacol. 2007 Dec;22(8):501-4. doi: 10.1002/hup.875.
7
Analysis of genetic variations in the dopamine D1 receptor (DRD1) gene and antipsychotics-induced tardive dyskinesia in schizophrenia.分析多巴胺 D1 受体(DRD1)基因的遗传变异与精神分裂症抗精神病药物所致迟发性运动障碍的关系。
Eur J Clin Pharmacol. 2011 Apr;67(4):383-388. doi: 10.1007/s00228-010-0967-2. Epub 2010 Dec 22.
8
Association of the Ser9Gly polymorphism in the dopamine D3 receptor gene with tardive dyskinesia in Korean schizophrenics.韩国精神分裂症患者中多巴胺D3受体基因Ser9Gly多态性与迟发性运动障碍的关联
Psychiatry Clin Neurosci. 2002 Aug;56(4):469-74. doi: 10.1046/j.1440-1819.2002.01038.x.
9
Association study of the vesicular monoamine transporter gene SLC18A2 with tardive dyskinesia.SLC18A2 基因与迟发性运动障碍的关联研究。
J Psychiatr Res. 2013 Nov;47(11):1760-5. doi: 10.1016/j.jpsychires.2013.07.025. Epub 2013 Sep 6.
10
Associations between polymorphisms in the cannabinoid receptor 1 gene, cognitive impairments and tardive dyskinesia in a Chinese population with schizophrenia.中国精神分裂症患者中大麻素受体 1 基因多态性与认知障碍和迟发性运动障碍的关联。
Brain Res. 2023 Dec 15;1821:148579. doi: 10.1016/j.brainres.2023.148579. Epub 2023 Sep 20.

引用本文的文献

1
Genetic Factors Associated With Tardive Dyskinesia: From Pre-clinical Models to Clinical Studies.与迟发性运动障碍相关的遗传因素:从临床前模型到临床研究
Front Pharmacol. 2022 Jan 24;12:834129. doi: 10.3389/fphar.2021.834129. eCollection 2021.

本文引用的文献

1
Genetics of tardive dyskinesia.迟发性运动障碍的遗传学。
Int Rev Neurobiol. 2011;98:231-64. doi: 10.1016/B978-0-12-381328-2.00010-9.
2
Epidemiology and risk factors for (tardive) dyskinesia.(迟发性)运动障碍的流行病学和危险因素。
Int Rev Neurobiol. 2011;98:211-30. doi: 10.1016/B978-0-12-381328-2.00009-2.
3
No Evidence for an Association between Dopamine D2 Receptor Polymorphisms and Tardive Dyskinesia in Korean Schizophrenia Patients.在韩国精神分裂症患者中,没有多巴胺 D2 受体多态性与迟发性运动障碍之间关联的证据。
Psychiatry Investig. 2011 Mar;8(1):49-54. doi: 10.4306/pi.2011.8.1.49. Epub 2011 Mar 10.
4
Statistical power analyses using G*Power 3.1: tests for correlation and regression analyses.使用 G*Power 3.1 进行统计功效分析:相关和回归分析的检验。
Behav Res Methods. 2009 Nov;41(4):1149-60. doi: 10.3758/BRM.41.4.1149.
5
The DRD3 rs6280 polymorphism and prevalence of tardive dyskinesia: a meta-analysis.DRD3 rs6280 多态性与迟发性运动障碍的患病率:一项荟萃分析。
Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):57-66. doi: 10.1002/ajmg.b.30946.
6
Association study between glutathione S-transferase GST-M1, GST-T1, and GST-P1 polymorphisms and tardive dyskinesia.谷胱甘肽S-转移酶GST-M1、GST-T1和GST-P1基因多态性与迟发性运动障碍的关联研究。
Hum Psychopharmacol. 2009 Jan;24(1):55-60. doi: 10.1002/hup.988.
7
Manganese superoxide dismutase gene Ala-9Val polymorphism might be related to the severity of abnormal involuntary movements in Korean schizophrenic patients.锰超氧化物歧化酶基因丙氨酸-9缬氨酸多态性可能与韩国精神分裂症患者异常不自主运动的严重程度有关。
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Dec 12;32(8):1844-7. doi: 10.1016/j.pnpbp.2008.08.013. Epub 2008 Aug 28.
8
No association between the brain-derived neurotrophic factor gene Val66Met polymorphism and tardive dyskinesia in schizophrenic patients.脑源性神经营养因子基因Val66Met多态性与精神分裂症患者迟发性运动障碍之间无关联。
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Aug 1;32(6):1545-8. doi: 10.1016/j.pnpbp.2008.05.016. Epub 2008 May 29.
9
Analysis of genetic variations in the human Par-4 (PAWR) gene and tardive dyskinesia in schizophrenia.精神分裂症患者中人类Par-4(PAWR)基因的遗传变异与迟发性运动障碍的分析。
Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):439-40. doi: 10.1002/ajmg.b.30795.
10
Val158Met polymorphism in the catechol-O-methyltransferase (COMT) gene is not associated with tardive dyskinesia in schizophrenia.儿茶酚-O-甲基转移酶(COMT)基因中的Val158Met多态性与精神分裂症的迟发性运动障碍无关。
Neuropsychobiology. 2008;57(1-2):22-5. doi: 10.1159/000123118. Epub 2008 Apr 18.

PAWR 基因多态性与精神分裂症患者迟发性运动障碍无关。

No association between PAWR gene polymorphisms and tardive dyskinesia in schizophrenia patients.

机构信息

Department of Psychiatry, Korea University School of Medicine, Seoul, Korea.

出版信息

Psychiatry Investig. 2012 Jun;9(2):191-4. doi: 10.4306/pi.2012.9.2.191. Epub 2012 May 22.

DOI:10.4306/pi.2012.9.2.191
PMID:22707972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3372569/
Abstract

Tardive dyskinesia (TD) is a hyperkinetic movement disorder associated with the prolonged use of antipsychotic drugs. Since prostate apoptosis response 4 (Par-4) is a key ligand of the dopamine D2 receptor, the Par-4 gene (PAWR) is a good candidate gene to study in the context of TD susceptibility. We examined the association between PAWR gene polymorphisms and TD. Three single nucleotide polymorphisms of PAWR were selected for the analysis: rs7979987, rs4842318, and rs17005769. Two hundred and eighty unrelated Korean schizophrenic patients participated in this study (105 TD and 175 non-TD patients). Genotype/allele-wise and haplotype-wise analyses were performed. There were no significant differences in genotype and allele frequencies between the two groups. Haplotype analysis also did not reveal a difference between the two groups. Within the limitations imposed by the size of the clinical sample, these findings suggest that PAWR gene variants do not significantly contribute to an increased risk of TD.

摘要

迟发性运动障碍(TD)是一种与抗精神病药物长期使用相关的多动障碍。由于前列腺凋亡反应蛋白 4(Par-4)是多巴胺 D2 受体的关键配体,因此 Par-4 基因(PAWR)是研究 TD 易感性的一个很好的候选基因。我们研究了 PAWR 基因多态性与 TD 之间的关系。选择了 PAWR 的三个单核苷酸多态性进行分析:rs7979987、rs4842318 和 rs17005769。280 名无关的韩国精神分裂症患者参与了这项研究(105 名 TD 患者和 175 名非 TD 患者)。进行了基因型/等位基因分析和单倍型分析。两组间的基因型和等位基因频率无显著差异。单倍型分析也未显示两组间存在差异。在临床样本大小所限的范围内,这些发现表明 PAWR 基因变异并不显著增加 TD 的风险。