Influence of CYP2D6 and CYP2C19 gene variants on antidepressant response in obsessive-compulsive disorder

被引:41
作者
Brandl, E. J. [1 ,2 ]
Tiwari, A. K. [1 ,2 ]
Zhou, X. [2 ,3 ]
Deluce, J. [2 ,3 ]
Kennedy, J. L. [1 ,2 ]
Mueller, D. J. [1 ,2 ]
Richter, M. A. [1 ,2 ,3 ]
机构
[1] Ctr Addict & Mental Hlth, Dept Neurosci, Neurogenet Sect, Campbell Family Mental Hlth Res Inst, Toronto, ON, Canada
[2] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[3] Sunnybrook Hlth Sci Ctr, Dept Psychiat, Toronto, ON M4N 3M5, Canada
关键词
obsessive-compulsive disorder (OCD); pharmacogenetics; CYP2D6; CYP2C19; treatment response; EVIDENCE-BASED PHARMACOTHERAPY; SEROTONIN REUPTAKE INHIBITORS; JAPANESE PSYCHIATRIC-PATIENTS; CYTOCHROME-P450; 2D6; GENOTYPE; STAR-ASTERISK-D; PLASMA-CONCENTRATIONS; DEPRESSED-PATIENTS; THERAPEUTIC RESPONSE; CLINICAL-RESPONSE; ACTIVITY SCORE;
D O I
10.1038/tpj.2013.12
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Numerous studies have reported on pharmacogenetics of antidepressant response in depression. In contrast, little is known of response predictors in obsessive-compulsive disorder (OCD), a disorder with among the lowest proportion of responders to medication (40-60%). Our study is the largest investigation to date (N= 184) of treatment response and side effects to antidepressants in OCD based on metabolizer status for CYP2D6 and CYP2C19. We observed significantly more failed medication trials in CYP2D6 non-extensive compared with extensive metabolizers (P= 0.007). CYP2D6 metabolizer status was associated with side effects to venlafaxine (P= 0.022). There were nonsignificant trends for association of CYP2D6 metabolizer status with response to fluoxetine (P= 0.056) and of CYP2C19 metabolizer status with response to sertraline (P= 0.064). Our study is the first to indicate that CYP genes may have a role in antidepressant response in OCD. More research is required for a future clinical application of genetic testing, which could lead to improved treatment outcomes.
引用
收藏
页码:176 / 181
页数:6
相关论文
共 72 条
  • [1] A prospective study of 86 new patients with social anxiety disorder
    Allgulander, C
    Nilsson, B
    [J]. ACTA PSYCHIATRICA SCANDINAVICA, 2001, 103 (06) : 447 - 452
  • [2] [Anonymous], 2002, STRUCTURED CLIN INTE
  • [3] APA, 2007, PRACT GUID TREATM PA
  • [4] Metabolism of antidepressant and neuroleptic drugs by cytochrome p450s: Clinical and interethnic aspects
    Bertilsson, L.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2007, 82 (05) : 606 - 609
  • [5] Influence of the CYP2D6*4 polymorphism on dose, switching and discontinuation of antidepressants
    Bijl, Monique J.
    Visser, Loes E.
    Hofman, Albert
    Vulto, Arnold G.
    van Gelder, Teun
    Stricker, Bruno H. Ch.
    van Schaik, Ron H. N.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 (04) : 558 - 564
  • [6] Meta-analysis of the dose-response relationship of SSRI in obsessive-compulsive disorder
    Bloch, M. H.
    McGuire, J.
    Landeros-Weisenberger, A.
    Leckman, J. F.
    Pittenger, C.
    [J]. MOLECULAR PSYCHIATRY, 2010, 15 (08) : 850 - 855
  • [7] Composite Functional Genetic and Comedication CYP2D6 Activity Score in Predicting Tamoxifen Drug Exposure Among Breast Cancer Patients
    Borges, Silvana
    Desta, Zeruesenay
    Jin, Yan
    Faouzi, Azzouz
    Robarge, Jason D.
    Philip, Santosh
    Nguyen, Anne
    Stearns, Vered
    Hayes, Daniel
    Rae, James M.
    Skaar, Todd C.
    Flockhart, David A.
    Li, Lang
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 50 (04) : 450 - 458
  • [8] Genotypes of cytochrome P450 and clinical response to clomipramine in patients with major depression
    Bouchez, J
    Dumur, V
    Lhermitte, M
    Goudemand, M
    [J]. EUROPEAN PSYCHIATRY, 1995, 10 (08) : 410 - 412
  • [9] Brandl EJ, 2012, PHARMACOGENOMICS, V13, P71, DOI [10.2217/PGS.11.133, 10.2217/pgs.11.133]
  • [10] The cytochrome P450 2D6 (CYP2D6) enzyme polymorphism: Screening costs and influence on clinical outcomes in psychiatry
    Chen, SQ
    Chou, WH
    Blouin, RA
    Mao, ZP
    Humphries, LL
    Meek, C
    Neill, JR
    Martin, WL
    Hays, LR
    Wedlund, PJ
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (05) : 522 - 534