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中国临床药理学与治疗学 ›› 2025, Vol. 30 ›› Issue (11): 1524-1529.doi: 10.12092/j.issn.1009-2501.2025.10.009

• 临床药理学 • 上一篇    下一篇

儿童肾病综合征患者他克莫司血药浓度变异性与临床疗效关系评价及影响因素分析

常钊,周宇雪,张胜男,吕萌   

  1. 郑州大学附属儿童医院、河南省儿童医院郑州儿童医院药学部,郑州  450018,河南
  • 收稿日期:2025-01-03 修回日期:2025-04-02 出版日期:2025-11-26 发布日期:2025-12-04
  • 通讯作者: 吕萌,男,硕士,副主任药师,研究方向:儿童个体化药物治疗。 E-mail: lvmengyh@126.com
  • 作者简介:常钊,男,硕士,主管药师,研究方向:临床药理学研究。 E-mail: 434424482@qq.com
  • 基金资助:
    河南省医学科技攻关计划联合共建项目(LHGJ20250589)

Clinical efficacy and influence factors about intra-patient variation of tacrolimus concentration in children with nephrotic syndrome

CHANG Zhao, ZHOU Yuxue, ZHANG Shengnan, LV Meng    

  1. Department of Pharmacy, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital Zhengzhou Children's Hospital, Zhengzhou 450018, Henan, China 
  • Received:2025-01-03 Revised:2025-04-02 Online:2025-11-26 Published:2025-12-04

摘要:

目的:研究肾病综合征患儿他克莫司(Tac)稳态谷浓度(C0)个体内变异与临床疗效的关系,分析个体内变异的影响因素,为促进患儿个体化使用Tac提供参考。方法:回顾性收集2021年1月到2023年11月郑州大学附属儿童医院64例肾病综合征患儿基本信息、Tac用药情况、Tac-C0、相关实验指标和CYP3A5*3位点检测结果,分析Tac-C0个体内变异情况,研究其与临床疗效的关系及影响因素。结果:患儿Tac首剂量为0.01~0.14 mg·kg-1·d-1,初始C0为(4.42±3.03) ng/mL,仅15.63%的患儿达到目标浓度5~10 ng/mL。经用药调整后,达标率上升至62.07%(P<0.01)。治疗3个月和6个月时,达标率分别为50.00%和52.17%。治疗期间患儿个体内Tac-C0的变异系数(Tac-C0-CV)为37.75%±16.16%。治疗6个月后,临床总缓解率为89.58%。未缓解患儿的Tac-C0-CV显著高于缓解的患儿(P<0.05)。多元回归分析结果显示CYP3A5*3多态性和年龄是影响Tac-C0-CV的独立因素(P<0.05)。结论:儿童肾病综合征患者Tac-C0在个体内波动较大,个体内变异程度高的患儿临床疗效较差。Tac-C0-CV受CYP3A5*3和年龄的影响。患儿应注意血药浓度监测和基因型检测,以调整用药方案,降低变异度,提高临床疗效。

关键词: 儿童, 肾病综合征, 他克莫司, 血药浓度, 个体内变异

Abstract:

AIM: To explore the intra-patient variation of tacrolimus concentration in children with nephrotic syndrome, evaluate clinical efficacy and analyze the factors, in order to provide reference for promoting rational drug use in children. METHODS: Sixty-four children with nephrotic syndrome were followed up in our hospital from January 2021 to November 2023. Basic information, medication orders, tacrolimus concentration and CYP3A5*3 polymorphism were collected. Evaluate the clinical efficacy and analyze the factors affecting tacrolimus concentration intra-patient variation. RESULTS: Tacrolimus initial dose was 0.01-0.14 mg·kg-1·d-1. C0 was (4.42±3.03) ng/mL, only 15.63% of children in the target concentration. After medication adjustment, children in target concentration up to 62.07%. 50% and 52.17% of children reach the target concentration respectively at 3 and 6 months. The coefficient of variation (CV) about all Tac-C0 was 37.75%±16.16%. The overall remission rate was 89.58%. The CV of children with non-remission was significantly higher (P<0.05). Tac-C0-CV was affected by CYP3A5*3 polymorphism and age (P<0.05). CONCLUSION: Children with high CV have poor clinical efficacy. The Tac-C0-CV in children with nephrotic syndrome is affected by CYP3A5*3 and age. TDM and genotype testing should be paid more attention in order to adjust the medication.

Key words: children, nephrotic syndrome, tacrolimus, serum concentration, intra-patient variation

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