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
相关论文
共 50 条
  • [21] No significant effect of SLCO1B1 polymorphism on the pharmacokinetics of rosiglitazone and pioglitazone
    Kalliokoski, Annikka
    Neuvonen, Mikko
    Neuvonen, Pertti J.
    Niemi, Mikko
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 (01) : 78 - 86
  • [22] The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin
    Martin, Nicholas G.
    Li, Ka Wah
    Murray, Heather
    Putt, Wendy
    Packard, Chris J.
    Humphries, Steve E.
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2012, 73 (02) : 303 - 306
  • [23] SLCO1B1 polymorphism and sex affect the pharmacokinetics of pravastatin but not fluvastatin
    Niemi, Mikko
    Pasanen, Marja K.
    Neuvonen, Pertti J.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2006, 80 (04) : 356 - 366
  • [24] Influence of SLCO1B1 polymorphism on maintenance therapy for childhood leukemia
    Suzuki, Ryoko
    Fukushima, Hiroko
    Noguchi, Emiko
    Tsuchida, Masahiro
    Kiyokawa, Nobutaka
    Koike, Kazutoshi
    Ma, Enbo
    Takahashi, Hideto
    Kobayashi, Chie
    Nakajima-Yamaguchi, Ryoko
    Sakai, Aiko
    Saito, Makoto
    Iwabuchi, Atsushi
    Kato, Keisuke
    Nakao, Tomohei
    Yoshimi, Ai
    Sumazaki, Ryo
    Fukushima, Takashi
    PEDIATRICS INTERNATIONAL, 2015, 57 (04) : 572 - 577
  • [25] Different effects of SLCO1B1 polymorphism on the pharmacokinetics of atorvastatin and rosuvastatin
    Pasanen, M. K.
    Fredrikson, H.
    Neuvonen, P. J.
    Niemi, M.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2007, 82 (06) : 726 - 733
  • [27] PharmVar GeneFocus: SLCO1B1
    Ramsey, Laura B.
    Gong, Li
    Lee, Seung-Been
    Wagner, Jonathan B.
    Zhou, Xujia
    Sangkuhl, Katrin
    Adams, Solomon M.
    Straka, Robert J.
    Empey, Philip E.
    Boone, Erin C.
    Klein, Teri E.
    Niemi, Mikko
    Gaedigk, Andrea
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2023, 113 (04) : 782 - 793
  • [28] Effects of gemfibrozil and atorvastatin on the pharmacokinetics of repaglinide in relation to SLCO1B1 polymorphism
    Kalliokoski, A.
    Backman, J. T.
    Kurkinen, K. J.
    Neuvonen, P. J.
    Niemi, M.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2008, 84 (04) : 488 - 496
  • [29] SLCO1A2, SLCO1B1 and SLCO2B1 polymorphisms influences chloroquine and primaquine treatment in Plasmodium vivax malaria
    Sortica, Vinicius A.
    Lindenau, Juliana D.
    Cunha, Maristela G.
    Ohnishi, Maria Deise O.
    Ventura, Ana Maria R.
    Ribeiro-dos-Santos, A. ndrea K. C.
    Santos, Sidney E. B.
    Guimaraes, Luciano S. P.
    Hutz, Mara H.
    PHARMACOGENOMICS, 2017, 18 (15) : 1401 - 1411
  • [30] Different effects of SLCO1B1 polymorphism on the pharmacokinetics and pharmacodynamics of repaglinide and nateglinide
    Kalliokoski, Annikka
    Neuvonen, Mikko
    Neuvornen, Pertti J.
    Niemi, Mikko
    JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 48 (03): : 311 - 321