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环孢素A及 CYP3A5和MDR1基因多态性对异基因造血干细胞移植患者伏立康唑血药浓度的影响

Effect of cyclosporine a and polymorphisms in and on the concentration of voriconazole in patients undergoing allogeneic hematopoietic stem cell transplantation.

作者信息

Zeng Guangting, Shi Lihong, Li Huilan, Wang Linlin, Zhu Miaomiao, Luo Jia, Zhang Zanling

机构信息

Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, China.

Institute for Rational and Safe Medication Practices, National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Xenobiotica. 2020 May;50(5):614-619. doi: 10.1080/00498254.2019.1672907. Epub 2019 Oct 11.

DOI:10.1080/00498254.2019.1672907
PMID:31573401
Abstract
  1. Voriconazole is known to display highly variable pharmacokinetics affecting treatment efficacy and safety. This study aimed to identify the factors causing the variation of voriconazole concentration in patients with allogeneic hematopoietic stem cell transplantation.2. The data of patients was collected, including clinical characteristics and voriconazole concentrations. A total of 5 single nucleotide polymorphisms of 3 candidate genes () related to voriconazole metabolism were genotyped by MassArray method. The correlation between polymorphisms and voriconazole concentration was analyzed.3. A total of 244 voriconazole concentrations of 43 patients were included in this study. The voriconazole concentration was significantly correlated with patients' total bile acid ( = 0.001) and cyclosporin A ( < 0.001). The median concentration of the normal metabolizers was remarkably lower than poor metabolizers (0.86 vs 2.27 μg/mL). The median concentration of GG genotype carriers was significantly higher than that of GA genotype carriers ( = 0.026).4. The variability of voriconazole concentration is partially explained by total bile acid, metabolic types of . The voriconazole concentration of normal metabolizers is likely to be lower than 1.0 μg/mL and thus at risk of infection due to inadequate treatment.
摘要
  1. 已知伏立康唑的药代动力学具有高度变异性,会影响治疗效果和安全性。本研究旨在确定异基因造血干细胞移植患者中导致伏立康唑浓度变异的因素。

  2. 收集患者的数据,包括临床特征和伏立康唑浓度。采用MassArray方法对与伏立康唑代谢相关的3个候选基因()的5个单核苷酸多态性进行基因分型。分析多态性与伏立康唑浓度之间的相关性。

  3. 本研究共纳入43例患者的244个伏立康唑浓度数据。伏立康唑浓度与患者总胆汁酸(=0.001)和环孢素A(<0.001)显著相关。正常代谢者的中位浓度显著低于慢代谢者(0.86 vs 2.27μg/mL)。GG基因型携带者的中位浓度显著高于GA基因型携带者(=0.026)。

  4. 伏立康唑浓度的变异性部分由总胆汁酸、的代谢类型解释。正常代谢者的伏立康唑浓度可能低于1.0μg/mL,因此因治疗不足有感染风险。

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Effect of cyclosporine a and polymorphisms in and on the concentration of voriconazole in patients undergoing allogeneic hematopoietic stem cell transplantation.环孢素A及 CYP3A5和MDR1基因多态性对异基因造血干细胞移植患者伏立康唑血药浓度的影响
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Influencing risk factors of voriconazole-induced liver injury in Uygur pediatric patients undergoing allogeneic hematopoietic stem cell transplantation.
影响维吾尔族儿科患者异基因造血干细胞移植后伏立康唑肝损伤的危险因素。
BMC Pediatr. 2024 May 3;24(1):299. doi: 10.1186/s12887-024-04625-1.
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