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遗传变异对西罗莫司药代动力学和药效学的影响:系统评价。

Influence of genetic variants on the pharmacokinetics and pharmacodynamics of sirolimus: a systematic review.

机构信息

Department of Pediatric Hematology, Amalia Children's Hospital, Radboud university medical center, Geert Grooteplein Zuid 32, Nijmegen, 6525 GA, The Netherlands.

Radboudumc Center of Expertise Hemangiomas & Congenital Vascular Malformations Nijmegen, Amalia Children's Hospital, Radboud university medical center, Rene Descartes Dreef 1, Nijmegen, 6525 GL, The Netherlands.

出版信息

Pharmacogenomics. 2023 Jul;24(11):629-639. doi: 10.2217/pgs-2022-0147. Epub 2023 Aug 8.

Abstract

Sirolimus is an antiproliferative and immunosuppressive compound inhibiting the mTOR pathway, which is often activated in congenital low-flow vascular malformations. Studies have demonstrated the efficacy of sirolimus for this disease. Studies in kidney transplant patients suggest that genetic variants can influence these pharmacokinetic parameters. Therefore, a systematic literature search was performed to gain insight into pharmacogenetic studies with sirolimus. Most studies investigated  and , with inconsistent results. No pharmacogenetic studies focusing on sirolimus have been performed for low-flow vascular malformations. We analyzed two common variants of and ( and , respectively) in patients (n = 59) with congenital low-flow vascular malformations treated with sirolimus. No association with treatment outcome was identified in this small cohort of patients.

摘要

西罗莫司是一种抗增殖和免疫抑制化合物,可抑制 mTOR 通路,该通路在先天性低流量血管畸形中经常被激活。研究已经证明了西罗莫司治疗这种疾病的疗效。肾移植患者的研究表明,遗传变异可能会影响这些药代动力学参数。因此,进行了系统的文献检索,以深入了解西罗莫司的药物遗传学研究。大多数研究都调查了和,结果不一致。没有针对低流量血管畸形的西罗莫司药物遗传学研究。我们分析了 59 例接受西罗莫司治疗的先天性低流量血管畸形患者中常见的和两个变体(和,分别)。在这个小患者队列中,没有发现与治疗结果有关的关联。

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