The influence of co-treatment with carbamazepine, amiodarone and statins on warfarin metabolism and maintenance dose

被引:38
作者
Herman, D
Locatelli, I
Grabnar, I
Peternel, P
Stegnar, M
Lainscak, M
Mrhar, A
Breskvar, K
Dolzan, V
机构
[1] Fac Med, Inst Biochem, SI-1000 Ljubljana, Slovenia
[2] Fac Pharm, Ljubljana, Slovenia
[3] Univ Med Ctr, Dept Vasc Dis, Ljubljana, Slovenia
[4] Gen Hosp Murska Sobota, Dept Internal Med, Murska Sobota, Slovenia
关键词
anticoagulant therapy; drug-drug interaction; warfarin pharmacokinetics;
D O I
10.1007/s00228-006-0104-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: Warfarin is a frequently used anticoagulant drug with narrow therapeutic index and high interindividual variability in the dose requirement. We have previously shown that warfarin dose is influenced by cytochrome P450 (CYP) 2C9 genotype, age, body weight and co-treatment with drugs that interfere with warfarin metabolism. As, in many patients, drug co-treatment cannot be avoided, we investigated the effect of co-treatment with carbamazepine, amiodarone and statins on warfarin metabolism and maintenance dose. Methods: Caucasian patients on stable maintenance warfarin therapy with CYP2C9*1/*1 genotype (n=82) were included in the study. Plasma concentrations of (S)- and (R)-warfarin as well as warfarin hydroxylated metabolites were determined using HPLC assay and corresponding clearances of (S)- and (R)-warfarin were calculated. Results: Patients co-treated with carbamazepine (n=5) had significantly higher plasma 10-hydroxywarfarin concentrations than patients not taking any interacting drugs (n=54) (median: 0.327 mu g/ml vs 0.030 mu g/ml, p=0.003). (S)- and (R)-warfarin clearances were also higher in the carbamazepine co-treated group (p=0.003), as were warfarin dose requirements (median: 9.00 mg/day vs 3.86 mg/day, p=0.003). Under the conditions of this study, patients co-treated with amiodarone (n=6) did not differ significantly regarding any measured characteristic from patients with no interacting drug treatment, while patients co-treated with simvastatin or lovastatin (n=17) had lower 10-hydroxywarfarin concentration (p=0.02). Conclusions: We confirmed important interaction between carbamazepine and warfarin metabolism which can be of major clinical importance. If treatment with carbamazepine cannot be avoided, patients taking warfarin should be frequently monitored, especially when initiating or stopping carbamazepine therapy.
引用
收藏
页码:291 / 296
页数:6
相关论文
共 40 条
[31]   DANGERS OF AMIODARONE AND ANTI-COAGULANT TREATMENT [J].
REES, A ;
DALAL, JJ ;
REID, PG ;
HENDERSON, AH ;
LEWIS, MJ .
BRITISH MEDICAL JOURNAL, 1981, 282 (6278) :1756-1757
[32]   Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose [J].
Rieder, MJ ;
Reiner, AP ;
Gage, BF ;
Nickerson, DA ;
Eby, CS ;
McLeod, HL ;
Blough, DK ;
Thummel, KE ;
Veenstra, DL ;
Rettie, AE .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (22) :2285-2293
[33]  
ROSS JR, 1980, BRIT MED J, V208, P1415
[34]   Clinical observations with the amiodarone/warfarin interaction - Dosing relationships with long-term therapy [J].
Sanoski, CA ;
Bauman, JL .
CHEST, 2002, 121 (01) :19-23
[35]   Influence of CYP2C9 and CYP2C19 genetic polymorphisms on warfarin maintenance dose and metabolic clearance [J].
Scordo, MG ;
Pengo, V ;
Spina, E ;
Dahl, ML ;
Gusella, M ;
Padrini, R .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2002, 72 (06) :702-710
[36]   The frequency and effects of cytochrome P450 (CYP) 2C9 polymorphisms in patients receiving warfarin [J].
Tabrizi, AR ;
Zehnbauer, BA ;
Borecki, IB ;
McGrath, SD ;
Buchman, TG ;
Freeman, BD .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2002, 194 (03) :267-273
[37]   Influence of cytochrome P-450CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment [J].
Taube, J ;
Halsall, D ;
Baglin, T .
BLOOD, 2000, 96 (05) :1816-1819
[38]   AMIODARONE REDUCES PLASMA WARFARIN CLEARANCE IN MAN [J].
WATT, AH ;
STEPHENS, MR ;
BUSS, DC ;
ROUTLEDGE, PA .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 20 (06) :707-709
[39]   Validation of methods for CYP2C9 genotyping:: Frequencies of mutant alleles in a Swedish population [J].
Yasar, Ü ;
Eliasson, E ;
Dahl, ML ;
Johansson, I ;
Ingelman-Sundberg, M ;
Sjoqvist, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (03) :628-631
[40]   A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity [J].
Yuan, HY ;
Chen, JJ ;
Lee, MTM ;
Wung, JC ;
Chen, YF ;
Charng, MJ ;
Lu, MJ ;
Hung, CR ;
Wei, CY ;
Chen, CH ;
Wu, JY ;
Chen, YT .
HUMAN MOLECULAR GENETICS, 2005, 14 (13) :1745-1751