Utility and adoption of CYP2D6 and CYP2C19 genotyping and its translation into psychiatric clinical practice

被引:23
作者
Jurgens, G. [1 ,2 ]
Jacobsen, C. B. [3 ]
Rasmussen, H. B. [2 ]
Werge, T. [2 ]
Nordentoft, M. [4 ]
Andersen, S. E. [1 ]
机构
[1] Bispebjerg Hosp, Dept Clin Pharmacol, DK-2400 Copenhagen NV, Denmark
[2] Copenhagen Univ Hosp, Mental Hlth Ctr Sct Hans, Res Inst Biol Psychiat, iPSYCH, Roskilde, Denmark
[3] Danish Inst Hlth Serv Res, Copenhagen, Denmark
[4] Copenhagen Univ Hosp, Psychiat Ctr Copenhagen, Res Unit, iPSYCH, Copenhagen, Denmark
关键词
CYP2D6; CYP2C19; psychiatry; INDUCED MOVEMENT-DISORDERS; DRUG; SCHIZOPHRENIA; PHARMACOKINETICS; ANTIDEPRESSANTS; ANTIPSYCHOTICS; POLYMORPHISMS; ALLELES; PHARMACOGENETICS; PHENOTYPE;
D O I
10.1111/j.1600-0447.2011.01802.x
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To describe clinical utility and adoption of routinely offered CYP2D6 and CYP2C19 genotyping (CYP test) in daily clinical practice of a psychiatric centre. Method: We described psychiatrists translations of CYP test results in patients with genotypes indicating poor or ultrarapid metabolizer status and treated with at least one CYP-dependent drug based on a retrospective review of medical records. Complementary, we used ethnographic participant observation and qualitative interviews to identify the barriers and incentives for the use of CYP test results. Results: The cohort study included 101 of 1932 cases genotyped between 2003 and 2009. In 53 of 101 cases, test results were addressed in medical records. The most frequent response was to monitor drug concentrations (23 cases), observe for adverse events (18 cases) and adjust dosage (13 cases). In 33 of 101 cases, results were mentioned in the discharge letter. The ethnographic study indicated a poor adoption of the CYP test in clinical praxis. Test results were lost in workflows and knowledge transfer between laboratory and clinician and were absent from clinical routines, treatment conferences and educational fora. Conclusion: The CYP test has not gained foothold in clinical practice, and its potential clinical benefits are not utilized.
引用
收藏
页码:228 / 237
页数:10
相关论文
共 33 条
[1]   Nonfunctional CYP2D6 alleles and risk for neuroleptics-induced movement disorders in schizophrenic patients [J].
Andreassen, OA ;
MacEwan, T ;
Gulbrandsen, AK ;
McCreadie, RG ;
Steen, VM .
PSYCHOPHARMACOLOGY, 1997, 131 (02) :174-179
[2]   Antipsychotic drug-Induced movement disorders in schizophrenics in relation to CYP2D6 genotype [J].
Armstrong, M ;
Daly, AK ;
Blennerhassett, R ;
Ferrier, N ;
Idle, JR .
BRITISH JOURNAL OF PSYCHIATRY, 1997, 170 :23-26
[3]  
Blue Cross and Blue Shield Association Technology Evaluation Center, 2004, SPEC REP GEN CYT CRO
[4]  
Cohen AP, 1987, ETHNOGRAPHIC RES GUI, P216
[5]   Low adoption of pharmacogenetic testing: an exploration and explanation of the reasons in Australia [J].
Corkindale, David ;
Ward, Helena ;
McKinnon, Ross .
PERSONALIZED MEDICINE, 2007, 4 (02) :191-199
[6]   CYP2D6*3, *4, *5 and *6 polymorphisms and antipsychotic-induced extrapyramidal side-effects in patients receiving antipsychotic therapy [J].
Crescenti, Anna ;
Mas, Sergi ;
Gasso, Patricia ;
Parellada, Eduard ;
Bernardo, Miquel ;
Lafuente, Amalia .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2008, 35 (07) :807-811
[7]   The CYP2D6 poor metabolizer phenotype may be associated with risperidone adverse drug reactions and discontinuation [J].
de Leon, J ;
Susce, MT ;
Pan, RM ;
Fairchild, M ;
Koch, WH ;
Wedlund, PJ .
JOURNAL OF CLINICAL PSYCHIATRY, 2005, 66 (01) :15-27
[8]  
Den Lokale Laegemiddelkomite, 2006, H S SCT HANS HOSP IN
[9]  
Fargher EA, 2005, PHARMACOECONOMICS, V23, P299
[10]   The clinical effectiveness and cost-effectiveness of testing for cytochrome P450 polymorphisms in patients with schizophrenia treated with antipsychotics: a systematic review and economic evaluation [J].
Fleeman, N. ;
McLeod, C. ;
Bagust, A. ;
Beale, S. ;
Boland, A. ;
Dundar, Y. ;
Jorgensen, A. ;
Payne, K. ;
Pirmohamed, M. ;
Pushpakom, S. ;
Walley, T. ;
de Warren-Penny, P. ;
Dickson, R. .
HEALTH TECHNOLOGY ASSESSMENT, 2010, 14 (03) :1-+