Urinary coproporphyrin I/(I plus III) ratio as a surrogate for MRP2 or other transporter activities involved in methotrexate clearance

被引:18
作者
Benz-de Bretagne, Isabelle [1 ,2 ]
Zahr, Noel [3 ]
Le Gouge, Amelie [4 ,5 ]
Hulot, Jean-Sebastien [3 ,6 ]
Houillier, Caroline [7 ]
Khe Hoang-Xuan [7 ]
Gyan, Emmanuel [8 ]
Lissandre, Severine [8 ]
Choquet, Sylvain [9 ]
Le Guellec, Chantal [1 ,2 ]
机构
[1] CHRU Tours, Lab Biochim & Biol Mol, Tours, France
[2] Univ Tours, PRES Ctr Val de Loire Univ, EA4245, Tours, France
[3] CHU Pitie Salpetriere, AP HP, Serv Pharmacol, Paris, France
[4] CHRU Tours, Ctr Invest Clin, Tours, France
[5] Univ Tours, PRES Ctr Val de Loire Univ, Inserm 202, Tours, France
[6] Univ Paris 06, UMR S 956, Paris, France
[7] CHU Pitie Salpetriere, AP HP, Serv Neurol, Ctr Expert Natl LOC, Paris, France
[8] CHRU Tours, Serv Hematol & Therapie Cellulaire, Tours, France
[9] CHU Pitie Salpetriere, AP HP, Serv Hematol, Paris, France
关键词
benzimidazole; drug transporters; drug-drug interactions; methotrexate; MRP2 (multi-drug resistance protein-2)/ABCC2; population pharmacokinetics; ORGANIC ANION-TRANSPORTER; HIGH-DOSE METHOTREXATE; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; CANCER RESISTANCE PROTEIN; GENETIC POLYMORPHISMS; ABCC2; MRP2; IN-VIVO; POPULATION PHARMACOKINETICS; BILIARY-EXCRETION; HEPATIC-UPTAKE;
D O I
10.1111/bcp.12326
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
AIMS The urinary coproporphyrin I/(I + III) ratio may be a surrogate for MRP2 activity. We conducted a prospective study in patients receiving methotrexate (MTX) to examine the relationship between this ratio and the pharmacokinetics of a MRP2 substrate. METHODS Three urine samples were collected from 81 patients for UCP I/(I + III) ratio determination: one before (P1), one at the end of MTX infusion (P2), and one on the day of hospital discharge (P3). Three polymorphisms of ABCC2 were analysed and their relationships with basal UCP I/(I + III) ratio values assessed. All associated drugs were recorded and a drug interaction score (DIS) was assigned. Population pharmacokinetic analysis was conducted to assess whether MTX clearance (MTXCL) was associated with the basal UCP I/(I + III) ratio, its variation during MTX infusion, the DIS or other common covariates. RESULTS The basal UCP I/(I + III) ratio was not associated with ABCC2 polymorphisms and did not differ according to the DIS. Significant changes in the ratio were observed over time, with an increase between P1 and P2 and a decrease at P3 (P < 0.001). No association was found between basal UCP I/(I + III) ratio and MTXCL. The final model indicates that MTXCL was dependent on the change in the ratio between P1 and P3, DIS and creatinine clearance. CONCLUSION The basal UCP I/(I + III) ratio is not predictive of MTXCL. However, it is sensitive to the presence of MTX, so it is plausible that it reflects a function modified in response to the drug.
引用
收藏
页码:329 / 342
页数:14
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