Tacrolimus dose requirement in relation to donor and recipient ABCB1 and CYP3A5 gene polymorphisms in Chinese liver transplant patients

被引:102
作者
Wang Wei-lin [1 ]
Jin Jing [1 ]
Zheng Shu-sen [1 ]
Wu Li-hua [1 ]
Liang Ting-bo [1 ]
Yu Song-feng [1 ]
Yan Sheng [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Coll Med,Key Lab Combined Multiorgan Transplantat, Dept Hepatobiliary Pancreat Surg,Minist Publ Hlth, Hangzhou 310003, Peoples R China
关键词
D O I
10.1002/lt.20709
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim of this study was to investigate whether the heterogeneity in tacrolimus dose requirement is associated with ABCB1 and CYP3A5 gene polymorphisms in Chinese liver transplant patients during the first month after transplantation. ABCB1 and CYP3A5 genotyping was performed using the polymerase chain reaction restriction sites polymorphism-based procedure in Chinese liver transplant recipients (n = 50) and their corresponding donors (n = 50). Tacrolimus whole-blood trough concentrations were measured by immunoassays on the IMx analyzers (Abbott Diagnostics Laboratories, Abbott-Park, IL). Doses required to achieve target blood concentrations and dose-adjusted trough concentrations (concentration/dose [C/D] ratios) were compared among patients according to allelic status of ABCB1 and CYP3A5. The ABCB1 3435CC was observed in 23 subjects (23%), whereas 64 (64%) carried 3435CT and 13 (13%) carried 3435TT. The CYP3A5*1/*1 was observed in 13 subjects (13%), 50 (50%) carried *1/*3, and 37 (37%) carried *3/*3. The tacrolimus C/D ratios were obviously lower in recipients carrying ABCB1 3435CC genotype. For CYP3A5, recipients who received organs from CYP3A5*31*3 donors had higher C/D ratios. But the donors' ABCB1 and recipients' CYP3A5 genotype did not affect the recipients' pharmacokinetics. Analysis of the combination of recipients' ABCB1 and donors' CYP3A5 genotypes revealed that the tacrolimus C/D ratios were significantly lower in the ABCB1 3435CC-carrying recipients, regardless of donors' CYP3A5 genotype. In conclusion, our finding suggests that the recipients' ABCB1 and donors' CYP3A5 genotype affect the tacrolimus dose requirements. ABCB1 C3435T polymorphism is a major determinant of tacrolimus trough concentration in Chinese liver transplant recipients, and recipients with 3435CC genotype will require higher dose of tacrolimus.
引用
收藏
页码:775 / 780
页数:6
相关论文
共 19 条
[1]   Association of the multidrug resistance-1 gene single-nucleotide polymorphisms with the tacrolimus dose requirements in renal transplant recipients [J].
Anglicheau, D ;
Verstuyft, CL ;
Laurent-Puig, P ;
Becquemont, L ;
Schlageter, MH ;
Cassinat, B ;
Beaune, P ;
Legendre, C ;
Thervet, E .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (07) :1889-1896
[2]   Clinical aspects of the MDRI (ABCB1) gene polymorphism [J].
Eichelbaum, M ;
Fromm, MF ;
Schwab, M .
THERAPEUTIC DRUG MONITORING, 2004, 26 (02) :180-185
[3]   In vitro and pharmacophore insights into CYP3A enzymes [J].
Ekins, S ;
Stresser, DM ;
Williams, JA .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2003, 24 (04) :161-166
[4]   CYP3A5*1-carrying graft liver reduces the concentration/oral dose ratio of tacrolimus in recipients of living-donor liver transplantation [J].
Goto, M ;
Masuda, S ;
Kiuchi, T ;
Ogura, Y ;
Oike, F ;
Okuda, M ;
Tanaka, K ;
Inui, K .
PHARMACOGENETICS, 2004, 14 (07) :471-478
[5]  
Haehner BD, 1996, MOL PHARMACOL, V50, P52
[6]   The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients [J].
Haufroid, V ;
Mourad, M ;
Van Kerckhove, V ;
Wawrzyniak, J ;
De Meyer, M ;
Eddour, DC ;
Malaise, J ;
Lison, D ;
Squifflet, JP ;
Wallemacq, P .
PHARMACOGENETICS, 2004, 14 (03) :147-154
[7]   Genetic polymorphisms of the CYP3A4, CYP3A5, and MDR-1 genes and pharmacokinetics of the calcineurin inhibitors cyclosporine and tacrolimus [J].
Hesselink, DA ;
van Schaik, RHN ;
van der Heiden, IP ;
van der Werf, M ;
Gregoor, PJHS ;
Lindemans, J ;
Weimar, W ;
van Gelder, T .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2003, 74 (03) :245-254
[8]   Functional polymorphisms of the human multidrug-resistance gene:: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo [J].
Hoffmeyer, S ;
Burk, O ;
von Richter, O ;
Arnold, HP ;
Brockmöller, J ;
Johne, A ;
Cascorbi, I ;
Gerloff, T ;
Roots, I ;
Eichelbaum, M ;
Brinkmann, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3473-3478
[9]   Modulation of steady-state kinetics of digoxin by haplotypes of the P-glycoprotein MDR1 gene [J].
Johne, A ;
Köpke, K ;
Gerloff, T ;
Mai, I ;
Rietbrock, S ;
Meisel, C ;
Hoffmeyer, S ;
Kerb, R ;
Fromm, MF ;
Brinkmann, U ;
Eichelbaum, M ;
Brockmöller, J ;
Cascorbi, I ;
Roots, I .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2002, 72 (05) :584-594
[10]   Identification of functionally variant MDR1 alleles among European Americans and African Americans [J].
Kim, RB ;
Leake, BF ;
Choo, EF ;
Dresser, GK ;
Kubba, SV ;
Schwarz, UI ;
Taylor, A ;
Xie, HG ;
McKinsey, J ;
Zhou, S ;
Lan, LB ;
Schuetz, JD ;
Schuetz, EG ;
Wilkinson, GR .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 70 (02) :189-199