Clinical implementation of pharmacogenetics in kidney transplantation: calcineurin inhibitors in the starting blocks

被引:36
作者
Elens, Laure [1 ,2 ]
Bouamar, Rachida [3 ]
Shuker, Nauras [3 ]
Hesselink, Dennis A. [4 ]
van Gelder, Teun [3 ,4 ]
van Schaik, Ron H. N. [2 ]
机构
[1] Catholic Univ Louvain, LDRI, B-1200 Brussels, Belgium
[2] Univ Med Ctr, Erasmus MC, Dept Clin Chem, Rotterdam, Netherlands
[3] Univ Med Ctr, Erasmus MC, Dept Hosp Pharm, Rotterdam, Netherlands
[4] Univ Med Ctr, Erasmus MC, Dept Internal Med, Rotterdam, Netherlands
关键词
calcineurin inhibitors; ciclosporin; kidney transplantation; pharmacogenetics; tacrolimus; SINGLE-NUCLEOTIDE POLYMORPHISMS; TACROLIMUS TROUGH CONCENTRATIONS; RENAL-ALLOGRAFT RECIPIENTS; MDR1; ABCB1; POLYMORPHISMS; BLOOD MONONUCLEAR-CELLS; GENETIC-POLYMORPHISMS; DOSE REQUIREMENTS; CYP3A5; GENOTYPE; ACUTE REJECTION; CYCLOSPORINE-A;
D O I
10.1111/bcp.12253
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacogenetics has generated many expectations for its potential to individualize therapy proactively and improve medical care. However, despite the huge amount of reported genetic associations with either pharmacokinetics or pharmacodynamics of drugs, the translation into patient care is still slow. In fact, strong evidence for a substantial clinical benefit of pharmacogenetic testing is still limited, with a few exceptions. In kidney transplantation, established pharmacogenetic discoveries are being investigated for application in the clinic to improve efficacy and to limit toxicity associated with the use of immunosuppressive drugs, especially the frequently used calcineurin inhibitors (CNIs) tacrolimus and ciclosporin. The purpose of the present review is to picture the current status of CNI pharmacogenetics and to discuss the most promising leads that have been followed so far.
引用
收藏
页码:715 / 728
页数:14
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