Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis

被引:80
作者
Need, Anna C. [1 ]
Keefe, Richard S. E. [2 ]
Ge, Dongliang [1 ]
Grossman, Iris [1 ]
Dickson, Sam [1 ,3 ]
McEvoy, Joseph P. [2 ,4 ]
Goldstein, David B. [1 ]
机构
[1] Duke Univ, Ctr Human Genome Variat, Inst Genome Sci & Policy, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27708 USA
[3] N Carolina State Univ, Bioinformat Res Ctr, Raleigh, NC 27695 USA
[4] John Umstead Hosp, Butner, NC USA
关键词
schizophrenia; neurocognition; RIMS1; quetiapine; GRM8; discontinuation; INDUCED TARDIVE-DYSKINESIA; CHRONIC-SCHIZOPHRENIA; DRUG RESPONSE; RECEPTOR GENE; CLINICAL-USE; ASSOCIATION; POLYMORPHISM; NEUROCOGNITION; VARIANTS; MEMORY;
D O I
10.1038/ejhg.2008.264
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Phase 1 Schizophrenia trial compared the effectiveness of one typical and four atypical antipsychotic medications. Although trials such as CATIE present important opportunities for pharmacogenetics research, the very richness of the clinical data presents challenges for statistical interpretation, and in particular the risk that data mining will lead to false-positive discoveries. For this reason, it is both misleading and unhelpful to perpetuate the current practice of reporting association results for these trials one gene at a time, ignoring the fact that multiple gene-by-phenotype tests are being carried out on the same data set. On the other hand, suggestive associations in such trials may lead to new hypotheses that can be tested through both replication efforts and biological experimentation. The appropriate handling of these forms of data therefore requires dissemination of association statistics without undue emphasis on select findings. Here we attempt to illustrate this approach by presenting association statistics for 2769 polymorphisms in 118 candidate genes evaluated for 21 pharmacogenetic phenotypes. On current evidence it is impossible to know which of these associations may be real, although in total they form a valuable resource that is immediately available to the scientific community. European Journal of Human Genetics (2009) 17, 946-957; doi:10.1038/ejhg.2008.264; published online 21 January 2009
引用
收藏
页码:946 / 957
页数:12
相关论文
共 38 条
[1]   Interaction between NOTCH4 and catechol-O-methyltransferase genotypes in schizophrenia patients with poor response to typical neuroleptics [J].
Anttila, S ;
Illi, A ;
Kampman, O ;
Mattila, KM ;
Lehtimäki, T ;
Leinonen, E .
PHARMACOGENETICS, 2004, 14 (05) :303-307
[2]   Pharmacogenetics in Psychiatry: Are We Ready for Widespread Clinical Use? [J].
Arranz, Maria J. ;
Kapur, Shitij .
SCHIZOPHRENIA BULLETIN, 2008, 34 (06) :1130-1144
[3]   Pharmacogenetic prediction of clozapine response [J].
Arranz, MJ ;
Munro, J ;
Birkett, J ;
Bolonna, A ;
Mancama, D ;
Sodhi, M ;
Lesch, KP ;
Meyer, JFW ;
Sham, P ;
Collier, DA ;
Murray, RM ;
Kerwin, RW .
LANCET, 2000, 355 (9215) :1615-1616
[4]   Discovery and utilization of haplotypes for pharmacogenetic studies of psychotropic drug response [J].
Athanasiou, MC ;
Malhotra, AK ;
Xu, CB ;
Stephens, JC .
PSYCHIATRIC GENETICS, 2002, 12 (02) :89-96
[5]   Antipsychotic-induced tardive dyskinesia and polymorphic variations in COMT, DRD2, CYP1A2 and MnSOD genes:: a meta-analysis of pharmacogenetic interactions [J].
Bakker, P. R. ;
van Harten, P. N. ;
van Os, J. .
MOLECULAR PSYCHIATRY, 2008, 13 (05) :544-556
[6]   Antipsychotic-induced tardive dyskinesia and the Ser9Gly polymorphism in the DRD3 gene: A meta analysis [J].
Bakker, PR ;
van Harten, PN ;
van Os, J .
SCHIZOPHRENIA RESEARCH, 2006, 83 (2-3) :185-192
[7]   Interaction of COMT Val108/158 met genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia [J].
Bertolino, A ;
Caforio, G ;
Blasi, G ;
De Candia, M ;
Latorre, V ;
Petruzzella, V ;
Altamura, M ;
Nappi, G ;
Papa, S ;
Callicott, JH ;
Mattay, VS ;
Bellomo, A ;
Scarabino, T ;
Weinberger, DR ;
Nardini, M .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (10) :1798-1805
[8]  
Braff DL, 2008, WORLD PSYCHIATRY, V7, P11
[9]   Association of RGS2 and RGS5 variants with schizophrenia symptom severity [J].
Campbell, Daniel B. ;
Lange, Leslie A. ;
Skelly, Tara ;
Lieberman, Jeffrey ;
Levitt, Pat ;
Sullivan, Patrick F. .
SCHIZOPHRENIA RESEARCH, 2008, 101 (1-3) :67-75
[10]   Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia [J].
Campbell, Daniel B. ;
Ebert, Philip J. ;
Skelly, Tara ;
Stroup, T. Scott ;
Lieberman, Jeffrey ;
Levitt, Pat ;
Sullivan, Patrick F. .
BIOLOGICAL PSYCHIATRY, 2008, 63 (01) :32-41