影响小儿癫痫患者丙戊酸血浆浓度的因素以及丙戊酸个性化疗法中CYP2C9基因型的临床意义

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Therapeutic Drug Monitoring Pub Date : 2024-08-01 Epub Date: 2024-01-26 DOI:10.1097/FTD.0000000000001180
Bingsuo Ma, Kun Yang, Xinping Li, Ning Su, Ting Yu, Yan Zou, Xingmeng Xu, Fei Wang, Jingdong Cheng, Zijun Yan, Tong Chen, Liangming Zhang
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引用次数: 0

摘要

研究背景本研究旨在探讨影响儿童癫痫患者血浆丙戊酸(VPA)浓度的因素,以及CYP2C9基因多态性在使用治疗药物监测和药物基因学检测进行个性化用药中的临床意义:回顾性分析了2022年7月至2023年7月期间在我院接受治疗药物监测且符合纳入标准的癫痫患儿的病历。通过统计分析确定年龄、性别、血氨、肝功能、肾功能和其他特征是否会影响这些患者的 VPA 浓度与剂量比(CDRV)。为了研究 CYP2C9 多态性对 CDRV 的影响,研究人员采集了患者的 DNA 样本,并使用实时定量 PCR 鉴定了 CYP2C9 基因型:208名儿童癫痫患者的平均年龄为(5.50 ± 3.50)岁。在这些患者中,182 人具有 CYP2C9 *1/*1 基因型,平均 CDRV(微克.千克/毫升.毫克)为 2.64 ± 1.46;24 人具有 CYP2C9 *1/*3 基因型,平均 CDRV 为 3.28 ± 1.74;2 人具有 CYP2C9 *3/*3 基因型,平均 CDRV 为 6.46 ± 3.33。这 3 种基因型之间存在统计学差异(P < 0.05)。这些患者的 CDRV 受年龄、天冬氨酸氨基转移酶、总胆红素、直接胆红素、球蛋白、白蛋白/球蛋白比值、前白蛋白、肌酐和 CYP2C9 多态性的显著影响。此外,多变量线性回归分析确定总胆红素、直接胆红素和 CYP2C9 多态性是导致高 CDRV 的独立风险因素:结论:肝脏问题和 CYP2C9 基因突变会增加 VPA 水平。结论:肝脏问题和 CYP2C9 基因突变会增加 VPA 的水平,这强调了在为癫痫儿童开具 VPA 处方时考虑这些因素的重要性,从而提高治疗的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Influencing Plasma Concentrations of Valproic Acid in Pediatric Patients With Epilepsy and the Clinical Significance of CYP2C9 Genotypes in Personalized Valproic Acid Therapy.

Background: The aim of this study was to investigate the factors affecting plasma valproic acid (VPA) concentration in pediatric patients with epilepsy and the clinical significance of CYP2C9 gene polymorphisms in personalized dosing using therapeutic drug monitoring and pharmacogenetic testing.

Methods: The medical records of children with epilepsy who underwent therapeutic drug monitoring at our institution between July 2022 and July 2023 and met the inclusion criteria were reviewed. Statistical analysis was performed to determine whether age, sex, blood ammonia, liver function, kidney function, and other characteristics affected the concentration-to-dose ratio of VPA (CDRV) in these patients. To investigate the effect of CYP2C9 polymorphisms on CDRV, DNA samples were collected from patients and the CYP2C9 genotypes were identified using real-time quantitative PCR.

Results: The mean age of 208 pediatric patients with epilepsy was 5.50 ± 3.50 years. Among these patients, 182 had the CYP2C9 *1/*1 genotype, with a mean CDRV (mcg.kg/mL.mg) of 2.64 ± 1.46, 24 had the CYP2C9 *1/*3 genotype, with a mean CDRV of 3.28 ± 1.74, and 2 had the CYP2C9 *3/*3 genotype, with a mean CDRV of 6.46 ± 3.33. There were statistical differences among these 3 genotypes ( P < 0.05). The CDRV in these patients were significantly influenced by age, aspartate aminotransferase, total bilirubin, direct bilirubin, globulin, albumin/globulin ratio, prealbumin, creatinine, and CYP2C9 polymorphisms. In addition, multivariate linear regression analysis identified total bilirubin, direct bilirubin, and CYP2C9 polymorphisms as independent risk factors for high CDRV.

Conclusions: Liver problems and mutations in the CYP2C9 gene increase VPA levels. This underscores the importance of considering these factors when prescribing VPA to children with epilepsy, thereby enhancing the safety and efficacy of the therapy.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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