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
  • [31] Impact of UGT1A9 Polymorphism on Mycophenolic Acid Pharmacokinetic Parameters in Stable Renal Transplant Patients
    Mazidi, Talia
    Rouini, Mohammad-Reza
    Ghahremani, Mohammad-Hossein
    Dashti-Khavidaki, Simin
    Lessan-Pezeshki, Mahboob
    Ahmadi, Farrokh Lagha
    Salam-Zadeh, Jamshid
    Mandegary, Ali
    Gholami, Kheirollah
    IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2013, 12 (03): : 547 - 556
  • [32] SLCO1B1 genetic variation and hormone therapy in menopausal women
    Moyer, Ann M.
    de Andrade, Mariza
    Faubion, Stephanie S.
    Kapoor, Ekta
    Dudenkov, Tanda
    Weinshilboum, Richard M.
    Miller, Virginia M.
    MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2018, 25 (08): : 877 - 882
  • [33] The reduced function allele SLCO1B1 c.521T>C is of no practical relevance for the renal graft function over the first post-transplant year in patients treated with mycophenolic acid
    Skegro, Sandra Nad
    Penezic, Luka
    Simicevic, Livija
    Hudolin, Tvrtko
    Kastelan, Zeljko
    Bozina, Nada
    Trkulja, Vladimir
    PHARMACOGENETICS AND GENOMICS, 2024, 34 (07) : 226 - 235
  • [34] Impact of SLCO1B3 polymorphisms on clinical outcomes in lung allograft recipients receiving mycophenolic acid
    Tague, Laneshia K.
    Byers, Derek E.
    Hachem, Ramsey
    Kreisel, Daniel
    Krupnick, Alexander S.
    Kulkarni, Hrishikesh S.
    Chen, Catherine
    Huang, Howard J.
    Gelman, Andrew
    PHARMACOGENOMICS JOURNAL, 2020, 20 (01) : 69 - 79
  • [35] Mycophenolic acid population pharmacokinetics in Tunisian renal transplant recipients
    Gaies, E.
    El Jebari, H.
    Jebabli, N.
    Salouage, I.
    Trabelsi, S.
    Charfi, R.
    Lakhal, M.
    Klouz, A.
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2013, 27 : 70 - 70
  • [36] Comparison of genetic variations of the SLCO1B1, SLCO1B3, and SLCO2B1 genes among five ethnic groups
    Namgoong, Suhg
    Cheong, Hyun Sub
    Kim, Ji On
    Kim, Lyoung Hyo
    Na, Han Sung
    Koh, In Song
    Chung, Myeon Woo
    Shin, Hyoung Doo
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2015, 40 (03) : 692 - 697
  • [37] Effects of SLCO1B1 and SLCO1B3 Genetic Polymorphisms on Valsartan Pharmacokinetics in Healthy Korean Volunteers
    Song, Gonjin
    Chung, Jee-Eun
    Yee, Jeong
    Lee, Kyung-Eun
    Park, Kyungsoo
    Gwak, Hye-Sun
    JOURNAL OF PERSONALIZED MEDICINE, 2021, 11 (09):
  • [38] Effect of SLCO1B1 polymorphism on induction of CYP3A4 by rifampicin
    Niemi, Mikko
    Kivistoe, Kari T.
    Diczfalusy, Ulf
    Bodin, Karl
    Bertilsson, Leif
    Fromm, Martin F.
    Eichelbaum, Michel
    PHARMACOGENETICS AND GENOMICS, 2006, 16 (08) : 565 - 568
  • [39] The SLCO1B1*5 Genetic Variant Is Associated With Statin-Induced Side Effects
    Voora, Deepak
    Shah, Svati H.
    Spasojevic, Ivan
    Ali, Shazia
    Reed, Carol R.
    Salisbury, Benjamin A.
    Ginsburg, Geoffrey S.
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 54 (17) : 1609 - 1616
  • [40] Impact ofUGT2B7and ABCC2genetic polymorphisms on mycophenolic acid metabolism in Chinese renal transplant recipients
    Li, Li-qing
    Chen, Di-na
    Li, Chuan-jiang
    Li, Qing-ping
    Chen, Yan
    Fang, Ping
    Zheng, Ping
    Lu, Hui-jie
    Ye, De-mei
    Wan, Hao-yang
    Li, Jie
    Li, Liang
    PHARMACOGENOMICS, 2018, 19 (17) : 1323 - 1334