罗马尼亚肾移植患者他克莫司清除率分析。

IF 3.9 3区工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY

Biomedicines Pub Date : 2025-06-18 DOI:10.3390/biomedicines13061501

Corina Andreea Rotarescu, Ion Maruntelu, Ion Rotarescu, Alexandra-Elena Constantinescu, Ileana Constantinescu

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引用次数: 0

摘要

背景/目的：他克莫司是肾移植中关键的免疫抑制剂，但其高度的个体间药代动力学变异性使剂量复杂化。本研究旨在建立人群药代动力学模型，并确定解释变异的因素，以优化罗马尼亚肾移植受者的他克莫司治疗。方法：研究对象为Fundeni临床研究所（2022-2024）的106例肾移植受者。采用免疫分析法检测他克莫司血药水平，采用实时聚合酶链反应检测CYP3A4、CYP3A5和ABCB1基因多态性。结果：CYP3A4*1/*1.001影响清除率（RSE = 11.8%），而红细胞压积是影响室间清除率的重要协变量（RSE = 6.14%）。结论：将CYP3A4*1/*1.001基因型和红细胞压积纳入给药策略可改善治疗药物监测和个性化免疫抑制治疗。

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Analysis of Tacrolimus Clearance in Patients with Kidney Transplants from Romania.

Background/Objectives: Tacrolimus is a key immunosuppressant in kidney transplantation, but its high interindividual pharmacokinetic variability complicates dosing. This study aimed to develop a population pharmacokinetic model and identify the factors explaining variability to optimize tacrolimus therapy in Romanian kidney transplant recipients. Methods: The study included 106 kidney transplant recipients treated at Fundeni Clinical Institute (2022-2024). Tacrolimus blood levels were measured using immunoassays, while gene polymorphisms of CYP3A4, CYP3A5, and ABCB1 were identified by real-time polymerase chain reaction. Results: Patients with CYP3A4*1/*1.001 impact clearance (RSE = 11.8%), while hematocrit was a significant covariate for intercompartmental clearance (RSE = 6.14%). Conclusions: Incorporating CYP3A4*1/*1.001 genotype and hematocrit into dosing strategies can improve therapeutic drug monitoring and personalize immunosuppressive therapy.

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来源期刊

Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology

CiteScore

5.20

自引率

8.50%

发文量

2823

审稿时长

8 weeks

期刊介绍： Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.