期刊文献+

基于孕烷X受体基因多态性指导肾移植受者他克莫司的个体化用药 被引量:6

Guidance for Individual Administration of Tacrolimus in Kidney-transplanted Patients According to Pregnane X Receptor Genetic Polymorphism
原文传递
导出
摘要 目的:研究肾移植受者孕烷X受体(PXR-C24381A)基因多态性与他克莫司(FK506)给药剂量的关系。方法:采用聚合酶链反应(PCR)产物直接测序法对60例肾移植术后受者进行PXR-C24381A基因分型,采用酶联免疫吸附分析法(ELISA法)测定FK506的血药浓度,比较不同基因型患者FK506血药浓度与给药剂量比值(C/D值)的差异。结果:肾移植受者PXR-C24381A等位基因C的频率为75%,A的频率为25%。C/A基因型与C/C基因型患者C/D值显著高于A/A基因型患者(P<0.05)。结论:肾移植受者PXR-C24381A基因多态性与FK506血药浓度具有相关性,A/A基因型患者拟取得相似的血药浓度需要比C/A和C/C基因型患者服用更高剂量的FK506。 OBJECTIVE: To study the relationship between pregnane X receptor (PXR-C24381A) genetic polymorphism and dosage of tacrolimus (FKS06) in kidney-transplanted patients. METHODS: The PXR genotypes of 60 kidney-transplanted patients were determined by PCR- direct sequencing. Blood concentration of FKS06 was measured by ELISA. The blood concentration of FK506 in patients with different genotypes was compared with dosage (C/D ratio). RESULTS: The frequency of PXR-C24381A al- lele C was 75%, and that of allele A was 25%. C/D ratio of patients with A/A genotype was significantly lower than those with C/ A genotype or C/C genotype (P〈0.05). CONCLUSIONS: PXR-C24381A polymorphism is correlated with the blood concentration of FKS06 in kidney-transplanted patients. If the same blood concentration of FK506 is presented in three genotypes, patients with A/ A genotype should take higher dosage than those with C/C and C/A genotypes.
出处 《中国药房》 CAS CSCD 2013年第22期2049-2050,共2页 China Pharmacy
基金 深圳市科技计划资助项目(No.201203053)
关键词 他克莫司 基因多态性 血药浓度 剂量 Tacrolimus Genetic polymorphism Blood concentration Dosage
  • 相关文献

参考文献7

  • 1侯明明,侯颖,宋洪涛,王庆华,杨顺良,谭建明.肾移植患者CYP3A4基因多态性对他克莫司疗效和不良反应的影响[J].中国药房,2010,21(26):2427-2429. 被引量:31
  • 2Connor A, Prowse A, MacPhee I, et al. Generic tacrolim- us in renal transplantation: trough blood concentration as a surrogate for drug exposure[J]. Transplantation, 2012, 93(12):45. 被引量:1
  • 3Ogawa Y, Okamoto S, Kuwana M, et al. Successful treat- ment of dry eye in two patients with chronic graft-ver- sus-host disease with systemic administration of FKS06 and corticosteroids[J]. Cornea, 2001,20(4) :430. 被引量:1
  • 4Ashavaid TF, Raje HS, Shah BV, et al. Design of allele specific PCR for rapid detection of CYP3A5 (A6986G) and Mdr-1 (C3435T) polymorphisms[J]. Indian J Clin Biochem, 2011,26(1) : 18. 被引量:1
  • 5Siddiqi N, Marfo K. Clinically significant drug-drug inter- action between tacrolimus and phenobarbital: the price we pay[J]. J Pharm Pratt, 201 O, 23 ( 6 ) : 585. 被引量:1
  • 6Tanaka K, Lake J, Villamil F, et al. Comparison of cyclo- sporine microemulsion and tacrolimus in 39 recipients of living donor liver transplantation[J]. Liver Transpl, 2005, 11(11):1 395. 被引量:1
  • 7丁春雷,刘丽宏,马萍,李鹏飞.他克莫司治疗药物监测研究进展[J].中国药房,2008,19(20):1580-1583. 被引量:31

二级参考文献26

  • 1涂向东,江清华,兰风华.三种简易提取全血基因组DNA方法的比较[J].中国实验诊断学,2006,10(3):264-266. 被引量:29
  • 2Hoffmeyer S, Burk O, Von Richter O, et al. 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]. Proc Natl Acad Sci USA, 2000,97 ( 7 ) : 3 473. 被引量:1
  • 3Fukushima-Uesaka H, Saito Y, Watanabe H, et al. Halotypes of CYP3A4 and their close linkage with haplotypes in a Japanese population[J]. Hum Mutat, 2004, 23 (1) : 100. 被引量:1
  • 4Zahir H, Nand RA, Brown KF. Validation of methods to study the distribution and protein binding of taerolimus in human blood [J] . Journal of Pharmacological and Toxicological Methods, 2001,46(1) : 27. 被引量:1
  • 5Victor W,Oelleric HM.New developments in the immunosuppressive drug monitoring ofcyclosporine, tacrolimus, and azathioprine [J ] . Clinical Biochem istry, 2001, 34(1) :9. 被引量:1
  • 6Ihor B,Dawna D,Qais A. Effect of low and high fat meals on Tacrolimus absorption following 5 mg single oral doses to healthy human subjects [J]. Clin Pharmacol ,2001, 41(2) : 176. 被引量:1
  • 7Napoli KL.Is Microparticle enzyme linked immunoassay (MEIA) reliable for use in tacrolimus TDM? Comparison of MEIA to liquid chromatography with mass spectrometric detection using longitudinal trough samples from transplant Recipients[J ] . Ther Drug Monit, 2006,28(4) : 491. 被引量:1
  • 8Regazzi MB, Renaldi M, Molinaro M, et al. Clinical pharmacokinetics of tacrolimus in heart transplant recipients [J ]. Ther Drug Monit, 1999, 21(1) :2. 被引量:1
  • 9Borrows R, Chusney G, Loucaidou M, et al. Tacrolimus monitoring in renal transplantation: a comparison between high - performance liquid chromatography and immunoassay [J] .Transplantation Proceedings, 2005, 37(4) :1 733. 被引量:1
  • 10Chena YL, Hirabayashi H, Akhtar S, et al. Simultaneous determination of three isomeric metabolites of tacrolimus(FK506) in human whole blood and plasma using high performance liquid chromatography - tandem mass spectrometry [J ] .Journal of Chromatography B, 2006,830(2) :330. 被引量:1

共引文献60

同被引文献61

  • 1陈业辉,郑克立,陈立中,戴宇平,费继光,王长希,魏鸿蔼,王良圣,胡建波.口服他克莫司血药浓度-时间曲线下面积[J].中华泌尿外科杂志,2004,25(11):750-752. 被引量:10
  • 2Yong Yong SHI,Lin HE.SHEsis,a powerful software platform for analyses of linkage disequilibrium,haplotype construction,and genetic association at polymorphism loci[J].Cell Research,2005,15(2):97-98. 被引量:382
  • 3Kamdem LK,Streit F,Zanger UM. Contribution of CYP3A5 to the in vitro hepatic clearance of tacrolimus[J].Clinical Chemistry,2005,(08):1374-1381. 被引量:1
  • 4Bombail V,Taylor K,Gibson GG. Role of Sp1, C/EBP alpha, HNF3, and PXR in the basal- and xenobiotic-mediated regulation of the CYP3A4 gene[J].Drug Metabolism and Disposition,2004.525-535. 被引量:1
  • 5Azarpira N,Aghdaie MH,Behzad‐Behbahanie A. Association between cyclosporine concentration and genetic polymorphisms of CYP3A5 and MDR1 during the early stage after renal transplantation[J].Experimental and Clinical Transplantation,2006,(01):416-419. 被引量:1
  • 6Kamdem LK,Streit F,Zanger UM. Contribution of CYP3A5 to the in vitro hepatic clearance of tacrolimus[J].Clinical Chemistry,2005.1374-1381. 被引量:1
  • 7Ball SE,Scatina J,Kao J. Population distribution and effects on drug metabolism of a genetic variant in the 5'promoter region of CYP3A4[J].Clinical Pharmacology and Therapeutics,1999,(03):288. 被引量:1
  • 8Hesselink DA,van Schaik RH,van der Heiden IP. Genetic polymorphisms of the CYP3A4,CYP3A5,and MDR-1 genes and pharmacokinetics of the calcineurin inhibitors cyclosporine and tacrolimus[J].Clinical Pharmacology and Therapeutics,2003,(03):245-254. 被引量:1
  • 9Roy JN,Barama A,Poirier C. CYP3A4,CYP3A5,and MDR‐1 genetic influences on tacrolimus pharmacokinetics in renal transplant recipients[J].PHARMACOGENETICS AND GENOMICS,2006,(09):659-665.doi:10.1097/01.fpc.0000220571.20961.dd. 被引量:1
  • 10李丹滢;陈燕华;方芸.CYP3A4/5单倍体将影响他克莫司血药谷浓度[A]四川成都,2012149-153. 被引量:1

引证文献6

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部