SLCO1B1 genetic polymorphism influences mycophenolic acid tolerance in renal transplant recipients

被引:30
|
作者
Michelon, Hugues [2 ]
Koenig, Joerg [3 ]
Durrbach, Antoine [4 ]
Quteineh, Lina [2 ]
Verstuyft, Celine [2 ]
Furlan, Valerie [5 ]
Ferlicot, Sophie [6 ]
Letierce, Alexia [1 ]
Charpentier, Bernard [4 ]
Fromm, Martin F. [3 ]
Becquemont, Laurent [1 ,2 ]
机构
[1] Hop Bicetre, AP HP, Clin Res Unit URC Paris Sud, Le Kremlin Bicetre, Bicetre, France
[2] Univ Paris Sud, Bicetre Univ Hosp, AP HP, Dept Pharmacol, Le Kremlin Bicetre, Bicetre, France
[3] Univ Erlangen Nurnberg, Inst Expt & Clin Pharmacol, D-91054 Erlangen, Germany
[4] Univ Paris Sud, Bicetre Univ Hosp, AP HP, Dept Nephrol, Le Kremlin Bicetre, Bicetre, France
[5] Hop Bicetre, AP HP, Dept Pharm, Le Kremlin Bicetre, Bicetre, France
[6] Univ Paris Sud, Bicetre Univ Hosp, AP HP, Dept Pathol, Le Kremlin Bicetre, Bicetre, France
关键词
adverse drug reaction; genetic polymorphism; mycophenolic acid; OATP1B1; pharmacogenetics; renal transplantation; SLCO1B1; SINGLE-NUCLEOTIDE POLYMORPHISMS; ACUTE REJECTION; ALLOGRAFT RECIPIENTS; CLINICAL PHARMACOKINETICS; GLUCURONIDE METABOLITE; PLASMA-CONCENTRATIONS; PROMOTER REGION; OATP-C; MOFETIL; IMPACT;
D O I
10.2217/PGS.10.132
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: This study aimed to determine the influence of gene candidates on mycophenolic acid (MPA) response during the first year of renal transplantation. Materials & methods: A total of 218 renal transplant recipients who received MPA from the first day of transplantation at a fixed dose of 2 g/day were genotyped for ABCB1, ABCC2, UGT2BZ UGT1A9, SLCO1B1, SLCO1B3 and IMPDH1 polymorphisms. Clinical end points were MPA-related adverse drug reactions (ADRs) and acute rejection episodes during the first year post-transplantation. Results: After correction for multiple statistical testing, SLCO1B1 (encoding the hepatic uptake transporter OATP1B1) was the only gene associated with MPA-related ADRs, showing a 75% risk reduction in favor of a protective effect of the SLCO1B1*5 allele (p = 0.002). In vitro experiments showed that MPA metabolites MPA-phenyl-glucuronide and MPA-acyl-glucuronide are substrates of OATP1B1. Their transport was decreased in the presence of the variant transporter (OATP1B1*5). Conclusion: These results suggest for the first time that carriers of the SLCO1B1*5 allele seem to be protected from MPA-related ADRs.
引用
收藏
页码:1703 / 1713
页数:11
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