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CYP3A5*3 and POR*28 Genetic Variants Influence the Required Dose of Tacrolimus in Heart Transplant Recipients

机译:CYP3A5 * 3和POR * 28的遗传变异影响他克莫司在心脏移植受者中所需的剂量

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Background: After heart transplantation (HTx), the interindividual pharmacokinetic variability of immunosuppressive drugs represents a major therapeutic challenge due to the narrow therapeutic window between over-immunosuppression causing toxicity and under-immunosuppression leading to graft rejection. Although genetic polymorphisms have been shown to influence pharmacokinetics of immunosuppressants, data in the context of HTx are scarce. We thus assessed the role of genetic variation in CYP3A4, CYP3A5, POR, NR1I2, and ABCB1 acting jointly in immunosuppressive drug pathways in tacrolimus (TAC) and ciclosporin (CSA) dose requirement in HTx recipients.
机译:背景:心脏移植(HTx)后,免疫抑制药物的个体间药代动力学差异代表了主要的治疗挑战,因为过度免疫抑制导致毒性反应和免疫抑制不足导致移植物排斥反应之间的治疗窗口狭窄。尽管已经表明遗传多态性会影响免疫抑制剂的药代动力学,但关于HTx的数据却很少。因此,我们评估了遗传变异在HTx受体的他克莫司(TAC)和环孢菌素(CSA)剂量要求的免疫抑制药物途径中共同作用于CYP3A4,CYP3A5,POR,NR1I2和ABCB1的作用。

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