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World J Gastroenterol. Dec 28, 2013; 19(48): 9156-9173
Published online Dec 28, 2013. doi: 10.3748/wjg.v19.i48.9156
Published online Dec 28, 2013. doi: 10.3748/wjg.v19.i48.9156
Ref. | Study population | Transplant type/analysis of recipients, donors or both | Findings |
Provenzani et al[91] | 32 Caucasian | Liver recipients and donors | No influence of 3435C>T and 2677G>T SNPs on tacrolimus dose requirements |
Cho et al[84] | 70 Korean | Kidney recipients | No association between ABCB1 genotype and tacrolimus dose requirements |
Shi et al[66] | 216 Chinese | Liver recipients | No association between any ABCB1 SNPs and tacrolimus dose requirements or blood trough levels |
Jun et al[98] | 568 Korean | Kidney and liver recipients (n = 506), and liver donors (n = 62) | No correlation between ABCB1 genotype and tacrolimus dose-adjusted blood trough levels |
Gervasini et al[33] | 103 Spanish | Kidney recipients | None of the ABCB1 polymorphisms were associated with changes in dose-adjusted blood trough levels and in dose requirementsNo association between ABCB1 genotype and tacrolimus-induced toxicity |
Kuypers et al[104] | 304 Belgian | Kidney recipients | No significant impact of ABCB1 genotype on tacrolimus exposure parameters or dosing requirements |
Provenzani et al[92] | 101 Caucasian | Kidney (n = 50) and liver (n = 51, recipients and donors) | No ABCB1 influence on dosing in liver transplant patientsThose patients receiving kidney transplant carrying the 2677T/A allele required significantly higher doses than those patients with the wild type allele |
Goto et al[63] | 181 Japanese | Liver recipients and donors | In the first week after transplantation, the recipients with wild type ABCB1 allele had lower tacrolimus dose-adjusted blood trough levelsNo difference observed after 2 wk |
Herrero et al[43] | 71 Spanish | Kidney recipients | Patients with wild type ABCB1 alleles had more stable tacrolimus concentrations within the therapeutic range during the first 3 moOn the contrary, patients carrying the polymorphic ABCB1 alleles showed a mean increase in tacrolimus blood concentration of more than 60% |
Wei-Lin et al[88] | 50 Chinese | Liver recipients and donors | Recipients with the wild type ABCB1-3435CC allele had significantly higher tacrolimus dose requirements than those with C3435T at 1 and 2 wk and 1 mo after transplantation |
López-Montenegro Soria et al[97] | 35 Spanish | Kidney recipients | Wild type ABCB1 3435CC patients had 40% lower concentration/dose ratios than those patients with variant alleles |
Elens et al[99] | 150 Belgian | Liver donors | ABCB1 genetic polymorphisms significantly influence tacrolimus hepatic concentrations, but have no effect on tacrolimus blood levelsPatients with ABCB1 1236C>T polymorphism showed significantly better liver functions and lower Banff scores with respect to patients with the wild-type allele |
- Citation: Provenzani A, Santeusanio A, Mathis E, Notarbartolo M, Labbozzetta M, Poma P, Provenzani A, Polidori C, Vizzini G, Polidori P, D’Alessandro N. Pharmacogenetic considerations for optimizing tacrolimus dosing in liver and kidney transplant patients. World J Gastroenterol 2013; 19(48): 9156-9173
- URL: https://www.wjgnet.com/1007-9327/full/v19/i48/9156.htm
- DOI: https://dx.doi.org/10.3748/wjg.v19.i48.9156