期刊文献+

OCT2、MDR1基因多态性与婴幼儿万古霉素血药浓度及临床疗效的相关性研究 被引量:7

Effects of OCT2 and MDR1 gene polymorphisms on vancomycin concentration and clinical efficacy in infants
下载PDF
导出
摘要 目的:考察有机阳离子转运体2(OCT2)和多药耐药基因1(MDR1)的基因多态性与婴幼儿万古霉素稳态谷浓度及临床疗效的相关性。方法:收集91例万古霉素治疗的婴幼儿患者血样,酶免疫放大分析法测定万古霉素血药浓度,聚合酶链式反应(PCR)和DNA测序技术检测基因分型。比较OCT2 G808T(rs316019)和MDR1C3435T(rs1045642)不同基因型对万古霉素谷浓度及临床疗效的影响。结果:91例患者中,谷浓度达到10~20μg/mL的比例为16.5%;5~<10μg/mL和10~20μg/mL浓度范围万古霉素的临床有效率(88%,93.3%)显著高于5μg/mL以下浓度(44%)(P<0.05),同时5~<10μg/mL和10~20μg/mL浓度范围万古霉素的临床有效率相近。OCT2 G808T纯合突变型(TT)患者万古霉素谷浓度(10.15±2.35)μg/mL和谷浓度/剂量比(0.98±0.27)μg·mL^(-1)·mg^(-1)·kg均显著高于野生型(GG)患者(6.92±2.83)μg/mL和(0.59±0.22)μg·mL^(-1)·mg^(-1)·kg(P<0.05);同时,TT型患者临床有效率(100%)明显高于GG型(73.2%)(P<0.05);而MDR1 C3435T突变型和野生型患者的万古霉素谷浓度、谷浓度/剂量比及临床疗效相近(P>0.05)。结论:OCT2G808T基因突变可能与婴幼儿患者万古霉素的稳态谷浓度及临床疗效相关。 AIM: To study the effects of organic cation transporter 2( OCT2) and multidrug resistance gene 1( MDR1) gene polymorphisms on plasma concentration and clinical efficacy of vancomycin in infants. METHODS: Ninety-one infants that treated with vancomycin were recruited. The plasma concentrations of vancomycin were measured by enzyme multiplied immunoassay technique. The genotypes of OCT2 G808 T( rs316019) and MDR1 C3435 T( rs1045642) were determined by polymerase chain reaction followed with direct sequencing.The association between different genotypes and the concentrations and clinical efficacy of vancomycin were analyzed. RESULTS: There were 16. 5% patients which the concentration reached 10-20 μg/mL. The curative effect of 5- 10 μg/mL( 88%)and 10-20 μg/mL( 93. 3%) were significant higher than that of 5 μg/mL( 44%)( P 0. 05); and the curative effect of 5- 10 μg/mL and 10-20 μg/mL were similar. The plasma concentration( 10. 15± 2. 35) μg/mL and concentration/dose values( 0. 98 ± 0. 27) μg·mL^(-1)·mg^(-1)·kg of vancomycin in infants with OCT2 TT genotype were significantly increased than that of OCT2 GG genotypes( 6. 92 ±2. 83) μg/mL,( 0. 59 ± 0. 22) μg·mL^(-1)·mg^(-1)·kg( P 0. 05). Meanwhile,the clinical efficacy of vancomycin in TT genotype( 100%) was higher than that in GG genotype( 73. 2%)( P 0. 05).However,the concentration and clinical efficacy of vancomycin in the infants with mutant type and wild type of MDR1 C3435 T were similar( P 0. 05).CONCLUSION: OCT2 G808 T polymorphism is associated with the plasma concentrations and clinical efficacy of vancomycin in infants.
出处 《中国临床药理学与治疗学》 CAS CSCD 2018年第2期154-158,共5页 Chinese Journal of Clinical Pharmacology and Therapeutics
基金 福建省妇幼保健院科研课题(妇保院研15-15)
关键词 万古霉素 药物转运体 基因多态性 血药浓度 婴幼儿 vancomycin drug transporter pol-ymorphisms plasma concentration infant
  • 相关文献

参考文献4

二级参考文献68

  • 1Chalermrat Bunchorntavakul,Disaya Chavalitdhamrong.Bacterial infections other than spontaneous bacterial peritonitis in cirrhosis[J].World Journal of Hepatology,2012,4(5):158-168. 被引量:29
  • 2刘晓红.美国肝病学会关于“肝硬化腹水伴自发性细菌性腹膜炎”的实践指南[J].中国实用内科杂志,2007,27(8):565-567. 被引量:45
  • 3Choi YH, Yu AM. ABC transporters in multidrug re- sistance and pharmacokinetics, and strategies for drug development[J]. Curt Pharm Des, 2014, 20 (5): 793 -807.
  • 4Brambila-Tapia AJ. MDR1 ( ABCB1 ) polymorphisms : functional effects and clinical implications [J]. Rev Invest Clin, 2013, 65(5) : 445-454.
  • 5Kaya P, Gtindtiz U, Arpaci F, et al. Identification of polymorphisms on theMDR1 gene among Turkish popu- lation and their effects on multidrug resistance in acuteleukemia patients[J]. Am J Hematol, 2005, 80( 1 ) : 26-34.
  • 6Liu Y, Ji W, Yin Y, et al. The effects of splicing va- riant of PXR PAR-2 on CYP3A4 and MDR1 mRNA expressions I J ]. Clin Chim Acta, 2009, 403 (1/2) : 142-144.
  • 7Sakaeda T, Nakamura T, Okumura K. Pharmacoge- netics of drug transporters and its impact on the phar- macotherapy [ J ]. Curt Top Med Chem, 2004, 4 (13) : 1385-1398.
  • 8Fung KL, Gottesman MM. A synonymous polymor- phism in a common MDR1 (ABCB1) haplotype shapes protein function [ J]. Biochim Biophys Acta, 2009, 1794(5): 860-871.
  • 9Kassogue Y, Dehbi H, Nassereddine S, et al. Geno- type variability and haplotype frequency of MDR1 (ABCB1) gene polymorphism in Morocco [ J ]. DNA Cell Biol, 2013, 32(10) : 582-588.
  • 10Komar AA. Silent SNPs: impact on gene function and phenotype [ J ]. Pharmacogenomics, 2007, 8 ( 8 ) : 1075-1080.

共引文献347

同被引文献64

引证文献7

二级引证文献18

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