Genotype and Allele Frequencies of Drug-Metabolizing Enzymes and Drug Transporter Genes Affecting Immunosuppressants in the Spanish White Population

被引:13
|
作者
Boso, Virginia [1 ,2 ]
Herrero, Maria J. [1 ,2 ]
Buso, Enrique [3 ]
Galan, Juan [4 ]
Almenar, Luis [5 ]
Sanchez-Lazaro, Ignacio [5 ]
Sanchez-Plumed, Jaime [6 ]
Bea, Sergio [6 ]
Prieto, Martin [7 ]
Garcia, Maria [7 ]
Pastor, Amparo [8 ]
Sole, Amparo [8 ]
Poveda, Jose Luis [1 ]
Alino, Salvador F. [1 ,9 ,10 ]
机构
[1] Hosp Univ & Politecn La Fe, Serv Farm, Unidad Farmacogenet, Valencia 46026, Spain
[2] Univ Valencia, Inst Invest Sanitaria La Fe, E-46003 Valencia, Spain
[3] Univ Valencia, Unidad Cent Invest, E-46003 Valencia, Spain
[4] Hosp Univ & Politecn La Fe, Valencia 46026, Spain
[5] Hosp Univ & Politecn La Fe, Serv Cardiol, Valencia 46026, Spain
[6] Hosp Univ & Politecn La Fe, Serv Nefrol, Valencia 46026, Spain
[7] Inst Salud Carlos III, CIBER Liver & Digest Dis CIBERehd, Madrid, Spain
[8] Hosp Univ & Politecn La Fe, Unidad Trasplante Pulm, Valencia 46026, Spain
[9] Hosp Univ & Politecn La Fe, Unidad Farmacol Clin, Valencia 46026, Spain
[10] Univ Valencia, Fac Med, Dept Farmacol, Valencia, Spain
关键词
genetic polymorphism; allele frequency; immunosuppressant; CYP3A5; SINGLE-NUCLEOTIDE POLYMORPHISMS; METHYLENETETRAHYDROFOLATE REDUCTASE GENE; IMPLEMENTATION CONSORTIUM GUIDELINES; PHENOLIC GLUCURONIDE METABOLITE; TACROLIMUS DOSE REQUIREMENTS; MDR1; ABCB1; POLYMORPHISMS; MYCOPHENOLIC-ACID; PHARMACOGENETIC POLYMORPHISMS; CALCINEURIN INHIBITORS; ACUTE REJECTION;
D O I
10.1097/FTD.0b013e3182a94e65
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Interpatient variability in drug response can be widely explained by genetically determined differences in metabolizing enzymes, drug transporters, and drug targets, leading to different pharmacokinetic and/or pharmacodynamic behaviors of drugs. Genetic variations affect or do not affect drug responses depending on their influence on protein activity and the relevance of such proteins in the pathway of the drug. Also, the frequency of such genetic variations differs among populations, so the clinical relevance of a specific variation is not the same in all of them. In this study, a panel of 33 single nucleotide polymorphisms in 14 different genes (ABCB1, ABCC2, ABCG2, CYP2B6, CYP2C19, CYP2C9, CYP3A4, CYP3A5, MTHFR, NOD2/CARD15, SLCO1A2, SLCO1B1, TPMT, and UGT1A9), encoding for the most relevant metabolizing enzymes and drug transporters relating to immunosuppressant agents, was analyzed to determine the genotype profile and allele frequencies in comparison with HapMap data. A total of 570 Spanish white recipients and donors of solid organ transplants were included. In 24 single nucleotide polymorphisms, statistically significant differences in allele frequency were observed. The largest differences (>100%) occurred in ABCB1 rs2229109, ABCG2 rs2231137, CYP3A5 rs776746, NOD2/CARD15 rs2066844, TPMT rs1800462, and UGT1A9 rs72551330. In conclusion, differences were recorded between the Spanish and other white populations in terms of allele frequency and genotypic distribution. Such differences may have implications in relation to dose requirements and drug-induced toxicity. These data are important for further research to help explain interindividual pharmacokinetic and pharmacodynamic variability in response to drug therapy.
引用
收藏
页码:159 / 168
页数:10
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