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基于药物基因组学的选择性5-羟色胺再摄取抑制剂个体化治疗抑郁症 被引量:5

Individualized Therapy Depression of Selective Serotonin Reuptake Inhibitors Based on Pharmacogenomics
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摘要 选择性5-羟色胺再摄取抑制剂(SSRIs)是当前治疗抑郁症的一线药物,CYP2D6、CYP2C19基因多态性会影响SSRIs的代谢,进而影响其疗效与安全性。目前我国临床医师对抑郁症患者基于基因多态性的SSRIs个体化治疗实践相对较少。该文就CYP2D6、CYP2C19基因型及其对SSRIs治疗的影响进行综述,以期为抑郁患者的个体化治疗提供参考。 Selective serotonin reuptake inhibitors(SSRIs)are the first-line drugs in the treatment of depression.CYP2D6 and CYP2C19 gene polymorphisms may influence the metabolism of SSRIs.Thereby,they could affect drug safety and efficacy.At present,clinicians have few individualized SSRIs treatment practices for depression patients based on pharmacogenomics.This paper reviews the genotypes of CYP2D6 and CYP2C19 and their effects on SSRIs treatment,in order to provide a useful reference of individualized SSRIs for patients with depression.
作者 周长凯 徐龙 张斌 纪洪艳 邢晓敏 郭切 张莎莎 王文晓 邵延琳 于红霞 李静 荆凡波 ZHOU Changkai;XU Long;ZHANG Bin;JI Hongyan;XING Xiaomin;GUO Qie;ZHANG Shasha;WANG Wenxiao;SHAO Yanlin;YU Hongxia;LI Jing;JING Fanbo(Department of Pharmacy, the Affiliated Hospital of Qingdao University,Qingdao 266000,China)
出处 《医药导报》 CAS 北大核心 2021年第2期198-203,共6页 Herald of Medicine
基金 国家软科学研究计划项目(2010GXS5D231) 中国药学会科普研究重点项目(CMEI2020KPYJ00608)。
关键词 选择性5-羟色胺再摄取抑制剂 个体化治疗 药物基因组学 抑郁症 Selective serotonin reuptake inhibitors Individualized therapy Pharmacogenomics Depression
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  • 1陈丽霞,王志纲,爱民,李文标,程宇航,敖登格日勒,李浩军,王传跃.抑郁症患者细胞色素P4502C19基因型对阿米替林血药浓度及其去甲基代谢的影响[J].中国神经精神疾病杂志,2005,31(1):33-36. 被引量:5
  • 2欧洲药品管理局认为两类抗抑郁药不应超适应证用于儿童和青少年[J].中国药物警戒,2005,2(3):186-186. 被引量:2
  • 3闻芳.抗精神病药物应用中的性别差异[J].国际精神病学杂志,2006,33(3):183-186. 被引量:10
  • 4张亚同,傅得兴.艾司西酞普兰的药理及临床评价[J].中国新药杂志,2006,15(22):1979-1983. 被引量:46
  • 5Sogaard B,Mengel H,Rao N,et al.Tthe pharmacokineties of escitalopram after oral and intravenous administration of single and multiple doses to healthy subjects[J].J Clin Pharmacol,2005:45:1400-1406.
  • 6Hyttel J,Bogeso KP,Perregaard J,et al.The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer[J].J Neural Transm Gen Sect,1992; 88:157-160.
  • 7Sanchez C,Brennum L.The S-enantiomer of citalopram (Lu 26 -054) is a highly selective and potent serotonin reuptake inhibitor[J].Biol Psychiatry,2000; 47:885.
  • 8de Morais SM,Wilkinson GR,Blaisdell J,et al.The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans[J].J Biol Chem,1994; 269:15419-15422.
  • 9Hyttel J.Pharmacological characterization of selective serotonin reuptake inhibitor (SSRIs)[J].Int Clin Psychopyarmacol,1994; 9(Suppl.1):S19 -S26.
  • 10Von Moltke LL,Greenblatt DJ,Giancarlo GM,et al.Escitalopram (S-citalopram) and its metabolites in vitro:Cytochromes mediating biotransformation,inhibitory effects,and comparison to R-citalopram[J].Drug Metab Dispos,2001; 29:1102-1109.

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