UGT1A9 -275T>A/-2152C>T Polymorphisms Correlate With Low MPA Exposure and Acute Rejection in MMF/Tacrolimus-Treated Kidney Transplant Patients
Clinical Pharmacology and Therapeutics , Volume 86 - Issue 3 p. 319- 327
Mycophenolate mofetil (MMF) is an immunosuppressive drug commonly used in the context of kidney transplantation. Exposure to the active metabolite mycophenolic acid (MPA) is associated with risk of allograft rejection. MPA pharmacokinetics varies between individuals, the potential cause being the presence of genetic polymorphisms in key enzymes. We genotyped 338 kidney transplant patients for UGT1A8, UGT1A9, UGT2B7, and MRP2 polymorphisms and recorded MPA exposure and biopsy-proven acute rejections (BPARs) during a 1-year follow-up. Tacrolimus-treated patients who were UGT1A9 -275T>A and/or -2152C>T carriers displayed a 20% lower MPA area under the concentration-time curve from 0 to 12 h (AUC0-12) (P = 0.012). UGT1A9*3 carriers displayed a 49% higher MPA AUC0-12 when treated with tacrolimus and a 54% higher MPA AUC0-12 when treated with cyclosporine (P < 0.005). Cyclosporine-treated UGT1A8*2/*2 (518GG) patients had an 18% higher MPA AUC0-12 compared with noncarriers. Carrying the UGT1A9 -275T>A and/or -2152C>T polymorphism significantly predicted acute rejection in fixed-dose (FD) MMF-treated patients receiving tacrolimus (odds ratio 13.3, 95% confidence interval 1.1-162.3; P < 0.05). UGT1A9 -275T>A and/or -2152C>T genotyping may identify patients at risk of MPA underexposure and acute rejection when receiving treatment with MMF and tacrolimus.Clinical Pharmacology & Therapeutics (2009); advance online publication 03 June 2009. doi:10.1038/clpt.2009.83.
|Clinical Pharmacology and Therapeutics|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
van Schaik, R.H.N, Agteren, M, de Fijter, J.W, Hartmann, A, Schmidt, J, Budde, K, … van Gelder, T. (2009). UGT1A9 -275T>A/-2152C>T Polymorphisms Correlate With Low MPA Exposure and Acute Rejection in MMF/Tacrolimus-Treated Kidney Transplant Patients. Clinical Pharmacology and Therapeutics, 86(3), 319–327. doi:10.1038/clpt.2009.83