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首页> 外文期刊>Transplantation Proceedings >Effect of MDR1 polymorphisms on the blood concentrations of tacrolimus in Turkish renal transplant patients
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Effect of MDR1 polymorphisms on the blood concentrations of tacrolimus in Turkish renal transplant patients

机译:MDR1多态性对土耳其肾移植患者他克莫司血药浓度的影响

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摘要

Background: Tacrolimus, a calcineurin inhibit?r, is prescribed to prevent allograft rejection in renal transplantation. Tacrolimus not only has a narrow therapeutic index, but also shows significant interindividual differences. The absorption and metabolism of this drug are affected by multidrug resistance (MDR) 1 gene polymorphisms that correlated with single-nucleotide polymorphisms (SNPs) affecting in vivo P-glycoprotein activity. This study investigated associations of MDR1 gene C3435T polymorphism with tacrolimus blood concentrations and dose requirements as well as acute rejection episodes among Turkish renal transplant patients. Methods: One hundred living-donor transplant recipients and 150 healthy control subjects underwent C3435T genotyping using polymerase chain reaction-restriction fragment length polymorphism. Blood concentrations of tacrolimus were determined with the cloned enzyme donor immunoassay. Results: The CC, CT, and TT genotype frequencies among patients were, respectively, 44.0%, 33.0%, and 23.0% versus 36.7%, 43.3%, and 20.0% among control subjects. There was no significant difference between (P =.061; P =.102; P =.211; respectively). The ratio of blood concentration to dose of tacrolimus for patients with mutant homozygous 3435 TT genotype was higher than that of wild-type 3435 CC genotype homozygous individuals. The doses for these patients were lower at 1, 3, and 12 months (P =.048; P =.03; P =.041, respectively). There were no significant differences between the groups regarding coprescription of drugs that affect tacrolimus concentrations, such as diltiazem. Acute rejection episodes were not associated with the CC vs CT or TT genotypes: odds ratio (OR), 0.517 (95% confidence interval [CI], 0.190-1.407; P =.192); OR 1.558 (95% CI, 0.587-4.136; P =.372); OR 1.346; (95% CI, 0.456-3.968; P =.590), respectively. Conclusions: Determination of MDR1 polymorphism may help to achieve target of tacrolimus blood concentrations.
机译:背景:他克莫司是一种钙调神经磷酸酶抑制剂,可预防肾移植中的同种异体移植排斥。他克莫司不仅具有狭窄的治疗指数,而且还表现出明显的个体差异。该药物的吸收和代谢受到多药耐药性(MDR)1基因多态性的影响,该基因多态性与影响体内P-糖蛋白活性的单核苷酸多态性(SNP)相关。这项研究调查了土耳其肾脏移植患者中MDR1基因C3435T多态性与他克莫司血药浓度和剂量要求以及急性排斥反应的相关性。方法:采用聚合酶链反应-限制性片段长度多态性对100例活体供体移植者和150例健康对照者进行C3435T基因分型。用克隆的酶供体免疫测定法测定他克莫司的血药浓度。结果:患者的CC,CT和TT基因型频率分别为44.0%,33.0%和23.0%,而对照组为36.7%,43.3%和20.0%。两者之间没有显着差异(分别为P = .061; P = .102; P = .211)。突变的纯合子3435 TT基因型患者的血药浓度与他克莫司的剂量之比高于野生型3435 CC基因型纯合子患者。这些患者的剂量在1、3和12个月时较低(分别为P = .048; P = .03; P = .041)。对于影响他克莫司浓度的药物(例如地尔硫卓)的共同处方,两组之间没有显着差异。急性排斥反应与CC vs CT或TT基因型无关:优势比(OR)为0.517(95%置信区间[CI]为0.190-1.407; P = .192);或1.558(95%CI,0.587-4.136; P = .372);或1.346; (95%CI,0.456-3.968; P = .590)。结论:MDR1基因多态性的测定可能有助于达到他克莫司血药浓度的目标。

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