首页> 外文期刊>Transplantation Proceedings >Pharmacogenetic study of ABCB1 and CYP3A5 genes during the first year following heart transplantation regarding tacrolimus or cyclosporine levels.
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Pharmacogenetic study of ABCB1 and CYP3A5 genes during the first year following heart transplantation regarding tacrolimus or cyclosporine levels.

机译:心脏移植后第一年中有关他克莫司或环孢素水平的ABCB1和CYP3A5基因的药物遗传学研究。

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摘要

Pharmacogenetics explains part of the interindividual variability in drug responses. Many published works about the effects of single nucleotide polymorphisms (SNPs) on immunosuppressive drug blood levels present contradictory results. We evaluated the SNPs in ABCB1 (glycoprotein P) and CYP3A5 (metabolic enzyme) genes, seeking correlate them with tacrolimus or cyclosporine levels during the first year after heart transplantation. One blood sample was obtained from each of 41 patients: 26 treated with cyclosporine and 15 with tacrolimus. We characterize the SNPs rs1045642, 1128503, 2032582, 2235013, 2235033, 2229109, 3213619, 9282564 in ABCB1 and rs10264272, 776746 in CYP3A5 genes using the Sequenom platform. The genotype was correlated with the trough drug blood levels corrected by dose and body weight (C(0)/(dose/weight)). The CYP3A5 SNPs showed the expected behavior, where patients carrying the low expression variants displayed higher drug blood levels of more than 100% of the normal expression variant level even at 1 year posttransplantation. To correlate ABCB1 SNPs, the variants described to cause higher blood levels in rs1045642, 1128503, 2032582 (in linkage disequilibrium) showed this effect only until 4 months posttransplantation among patients treated with cyclosporine (more than 100% higher than the other variant). After 1 year, concentrations reached a stable phase with normal levels. The observation was not so evident among those treated with tacrolimus. Remarkably, at this point, patients treated with cyclosporine, showed a significant (P < .01) difference between the two variants of rs9282564 and even if it was not significant there was also a tendency among the intronic rs2235013 and 2235033. The results indicated that SNPs in ABCB1 gene seem to not be relevant for long-term dose adjustment in patients, but to show an effect during the first 4 months.
机译:药物遗传学解释了药物反应中个体间差异的部分。许多发表的关于单核苷酸多态性(SNP)对免疫抑制药物血药浓度影响的著作提出了矛盾的结果。我们评估了心脏移植后第一年中ABCB1(糖蛋白P)和CYP3A5(代谢酶)基因中的SNP,以使其与他克莫司或环孢素水平相关。从41例患者中分别获取一份血液样本:用环孢霉素治疗26例,他克莫司治疗15例。我们使用Sequenom平台对ABCB1中的SNP rs1045642、1128503、2032582、2235013、2235033、2229109、3213619、9282654和CYP3A5基因中的rs10264272、776746进行了表征。基因型与通过剂量和体重(C(0)/(剂量/体重))校正的谷药血水平相关。 CYP3A5 SNPs表现出预期的行为,即使在移植后1年,携带低表达变异体的患者仍显示较高的药物血液水平,超过正常表达变异体水平的100%以上。为了使ABCB1 SNP相关,描述为在rs1045642、1128503、2032582中引起较高血液水平的变体(连锁不平衡)仅在使用环孢霉素治疗的患者移植后4个月才显示出这种效果(比另一变体高100%以上)。一年后,浓度达到稳定水平并达到正常水平。在使用他克莫司治疗的患者中观察不到那么明显。值得注意的是,此时,用环孢菌素治疗的患者在rs9282564的两个变体之间显示出显着(P <.01)差异,即使内含子rs2235013和2235033之间也存在趋势,结果表明: ABCB1基因中的SNP似乎与患者的长期剂量调整无关,但在头4个月内显示出作用。

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