期刊文献+

细胞色素P4502D6 C188T基因多态性与难治性抑郁症的关联 被引量:3

Association study of cytochrome p4502D6 gene polymorphism and treatment-resistant depression
下载PDF
导出
摘要 目的:探讨细胞色素P450(CYP)2D6 C188T基因多态性与难治性抑郁症及氟西汀合并小剂量利培酮治疗的疗效、不良反应的关联。方法:应用聚合酶链反应(PCR)扩增技术及限制性片段长度多态性(RFLP)测定92例难治性抑郁症患者及107名正常对照的CYP2D6 C188T基因多态性。其中59例患者接受氟西汀合并小剂量利培酮治疗6周,进一步分析不同疗效或不良反应患者的CYP2D6 C188T基因多态性。结果:难治性抑郁症患者与健康对照组CYP2D6C188T基因型及等位基因分布差异无统计学意义。36例有效患者的T等位基因频率(n=40,55.6%)高于23例无效患者的(n=14,30.4%),(χ2=7.14,P=0.01);33例有不良反应患者的T等位基因频率(n=46,69.7%)高于26例无不良反应患者的(n=26,50.0%),(χ2=4.74,P=0.03)。结论:CYP2D6 C188T基因多态性与难治性抑郁症无显著关联,但可能是影响利培酮对氟西汀增效作用以及两药联用的不良反应。 Objective:To investigate the association between cytochrome p450(CYP)2D6 C188T gene polymorphism and treatment-resistant depression and it's therapeutic response.Method:Polymerase chain reaction and restriction fragment length polymorphism techniques were used to examine the CYP2D6 C188T gene polymorphism of 92 treatment-resistant depression patients and 107 healthy controls.Within the patients,there were 59 accepted the risperidone augmentation of fluoxetine.Results:There was no significant difference between the treatment-resistant depression patients and the healthy controls in CYP2D6 C188T genotypes and alleles.According there response to the therapy,59 patients were divided into response and non-response groups.The frequency of T allele in treatment response group(n=40,55.6%) was significantly higher than the group of non-response(n=14,30.4%)(χ2=7.14,P=0.01).The T allele of CYP2D6 C188T of the patients who had side-effect(n=46,69.7%) was significantly higher than those who hadn't side-effect(n=26,50.0%)(χ2=4.74,P=0.03).Conclusion:The results suggested that there was no association with treatment-resistant depression and CYP2D6 C188T gene polymorphism.The T allele of CYP2D6 C188T may affect the augmentative effect and side effect of the risperidone to fluoxetine.
出处 《临床精神医学杂志》 2011年第4期226-229,共4页 Journal of Clinical Psychiatry
关键词 难治性抑郁症 多态性 细胞色素P4502D6 treatment-resistant depression polymorphism cytochrome p4502D6
  • 相关文献

参考文献16

  • 1DeVane CL. Pharmacogenetics and drug metabolism of newer anti- depressant agents [J]. J Clin Psychiat,1994,55:38-45. 被引量:1
  • 2Bertilsson L, Dahl ML, Dalen P, et al. Molecular genetics of CYP2D6 :clinical relevance with focus on psychotropic drugs [ J ]. Br J Clin Pharmacol,2002,53 : 111 -122. 被引量:1
  • 3Kirchheiner J, Seeringer A. Clinical implications of pharmacogenetics of cytoehrome P450 drug metabolizing enzymes [ J ]. Biochim Biophys Aeta,2007 ,1770 :489-494. 被引量:1
  • 4Rendic S, Di Carlo FJ. Human cytochrome P450 enzymes:a status report summarizing their reactions, substrates, inducers and inhibitons [ J]. Drug Metab Rev, 1997,29:413-550. 被引量:1
  • 5Fava M, Davidson KG. Definition and epidemiology of treatment - resistant depression [J]. Psychiat Clin North Am, 1996,19: 179- 200. 被引量:1
  • 6Caccia S. Metabolism of the newer antidepressants. An overview of the pharmacological and pharmacokinetic implications [ J ]. Clin Pharmacokinet, 1998,34:281-302. 被引量:1
  • 7Grasmader K, Verwohlt PL, Rietschel M, et al, Impact of polymor- phisms of cytochrome-P450 isoenzymes 2C9,2C19 and 2D6 on plasma concentrations and clinical effects of antidepressants in a naturalistic clinical setting [ J ]. Eur J Clin Pharmacol, 2004,60 : 329-336. 被引量:1
  • 8Serretti A, Calati R, Massat I, et al. Cytochrome P450 CYP1A2, CYP2C9, CYP2C19 and CYP2D6 genes are not associated with response and remission in a sample of depressive patients [ J ]. Int Clin Psychopharmacol. 2009,24:250-256. 被引量:1
  • 9陈静,陆峥,江三多,蔡军,钱伊萍,李霞.细胞色素P450酶1A2和2C19基因多态性与难治性抑郁症的关联分析[J].上海精神医学,2005,17(2):95-98. 被引量:11
  • 10李霞,陆峥,蔡军,熊祥玉,姚培芬,郭珍,刘帼芳,李华芳,林治光,江开达.利培酮对难治性抑郁症的辅助治疗作用[J].临床精神医学杂志,2002,12(5):259-260. 被引量:14

二级参考文献13

  • 1DeVane CL. Phannacogenetics and drug metabolism of newer antidepressant agents. J Clin Psychiatry. 1994, 55 : 38 -45. 被引量:1
  • 2Bcrtilsson L, Dahl ML, Dalen P, et al. Molecular genetics of CYP2D6: clinical relevance with focus on psychotropic drugs. Br J Clin Pharmacol. 2002, 53: 111 -22. 被引量:1
  • 3Rendic S, Di Carlo FJ. Human eytochrome P450 enzymes: A status report summarizing their reactions, substrates, inducers and inhibitors. Drug Metab Bey. 1997, 29:413 -580. 被引量:1
  • 4Carrillo JA, Dalai ML, Svensson JO. et al. Bertilsson, the polymorphic CYP2D6 and also by the CYP1A2 activity. Clin Pharmacol Ther.1996, 60:183- 190. 被引量:1
  • 5Hamelin BA, Turgeon J, Vallee J, et al. The disposition of fluoxetine but not semaline is alter in poor metabolizers of debrisoquin. Clin Pharmacol Ther. 1996, 60:512 -21. 被引量:1
  • 6Fjordside L, Jeppesen U, Eap CB, et al. The stereo-selective meotabolism of fluoxetine in poor and extensive metabolizers of sparteine.Phannacogenetics. 1999, 9:55 - 60. 被引量:1
  • 7Von MMoltke LL, Greeblatt DJ, Duan SX, et al. Human cytochromes mediating N - demethylation of fluoxetine in virtro. Psychophannacol.1997, 123:402-7. 被引量:1
  • 8Daniel WA, Kot M. Influence of classic and atypical neuroleptics on caffeine oxidation in rat liver microsomes. Wojcikowski J. Pol J Pharmacol. 2003 , 55:1055-61. 被引量:1
  • 9Ostroff RB, Nelson JC. Risperidone augmentation of selective serotonin reuptake inhibitors in major depression.J Clin Psychiatry,1999,60:256 被引量:1
  • 10Stoll AL,Haura G.Tranylcypromine plus risperidone for treatment-refractory major depression [letter].J Clin Psychopharmacol,2000,70:68 被引量:1

共引文献23

同被引文献30

  • 1苏林雁,耿耀国,王洪,杜亚松,孙凌,赵福涛,范方.注意缺陷多动障碍诊断量表父母版的中国城市儿童常模制定及其信度和效度的检验[J].中国实用儿科杂志,2006,21(11):833-836. 被引量:41
  • 2Michelson D,Allen AJ,Busner J,et al.Once-daily atomoxetine treatment for children and adolescents with attention deficit hyperactivity disorder:a randomized,placebo-controlled study[J].Am J Psychiatry,2002,159(11):1896-1901. 被引量:1
  • 3Kelsey DK,Sumner CR,Casat CD,et al.Once-daily atomoxetine treatment for children with attention-deficit/hyperactivity disorder,including anassessment of evening and morning behavior:a double-blind,placebo-controlled trial[J].Pediatrics,2004,114(1):e1-8. 被引量:1
  • 4Newcorn JH,Sutton VK,Weiss MD,etal.Clinical responses to atomoxetine in attention-deficit/hyperactivity disorder:the Integrated Data Exploratory Analysis(IDEA)study[J].J Am Acad Child Adolesc Psychiatry,2009,48(5):511-518. 被引量:1
  • 5American Psychiatric Association.Diagnostic and Statistical Manual of Mental Disorders:DSM-IV-TR[M].Washington,DC:American Psychiatric Association,2000:78-85. 被引量:1
  • 6龚耀先,蔡太生.中国修订韦氏智力儿童智力量表手册[M].长沙:湖南地图出版社,1993. 被引量:1
  • 7Stein MA,Sarampote CS,Waldman ID,et al.A dose-response study of OROS methylphenidate in children with attention-deficit/hyperactivity disorder[J].Pediatrics,2003,112:e404. 被引量:1
  • 8Steele M,Jensen PS,Quinn DM.Remission versus response as the goal of therapy in ADHD:a newstandard for the field?[J].Clin Ther,2006,28(11):1892-1908. 被引量:1
  • 9Samer CF,Lorenzini KI,Rollason V,et al.Applications of CYP450testing in the clinical setting[J].Mol Diagn Ther,2013,17(3):165-184. 被引量:1
  • 10Ramoz N,Boni C,Downing AM,et al.A haplotype of the norepinephrine transporter(Net)gene Slc6a2 is associated with clinical response to atomoxetine in attention-deficit hyperactivity disorder(ADHD)[J].Neuropsychopharmacology,2009,34(9):2135-2142. 被引量:1

引证文献3

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部