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中国临床药理学与治疗学 ›› 2025, Vol. 30 ›› Issue (10): 1383-1390.doi: 10.12092/j.issn.1009-2501.2025.10.010

• 临床药理学 • 上一篇    下一篇

炎症性肠病患者GST基因多态性与硫唑嘌呤活性代谢物6-TGN浓度水平相关性研究

董家珊1,陈嘉睿2,曾大勇2,刘亦伟2,许建文2,林荣芳2   

  1. 1厦门医学院附属第二医院药学部,厦门  361021,福建;2福建医科大学附属第一医院药学部,福州  350005,福建

  • 收稿日期:2024-11-21 修回日期:2025-02-24 出版日期:2025-10-26 发布日期:2025-10-15
  • 通讯作者: 林荣芳,女,硕士,主任药师,研究方向:医院药学与个体化给药。 E-mail: 33015631@qq.com
  • 作者简介:董家珊,女,硕士,主管药师,研究方向:医院药学与个体化给药。 E-mail: 462290027@qq.com
  • 基金资助:
    福建省卫生健康委员会青年科研课题(2022QNA037)

Correlation between GST gene polymorphism and concentration of azathioprine active metabolite 6-TGN in patients with inflammatory bowel disease

DONG Jiashan1, CHEN Jiarui2, ZENG Dayong2, LIU Yiwei2, XU Jianwen2, LIN Rongfang2   

  1. 1Department of Pharmacy , the Second Affiliated Hospital of Xiamen Medical College, Xiamen 361021, Fujian, China; 2Department of Pharmacy, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, Fujian, China
  • Received:2024-11-21 Revised:2025-02-24 Online:2025-10-26 Published:2025-10-15

摘要:

目的:探讨炎症性肠病(inflammation bowel disease,IBD)患者谷胱甘肽S转移酶(glutathione-S-transferase,GST)基因多态性对硫唑嘌呤(azathioprine,AZA)活性代谢物6-硫鸟嘌呤核苷酸(6-thioguanine nucleotides,6-TGN)浓度的影响,以期为优化患者AZA治疗方案提供参考。方法:前瞻性收集接受AZA治疗的IBD患者相关临床资料,给药前采用多重PCR技术结合高通量测序技术的靶向测序法测得患者GST-A1、GST-M1、GST-P1、GST-T1基因型,并应用HPLC法测定患者红细胞中6-TGN稳态谷浓度,利用SPSS 26.0软件进行统计分析。结果:研究共纳入90例IBD患者。GSTA1、GST-M1、GST-P1、GST-T1等位基因频率均符合Hardy-Weinberg平衡定律。Logistic回归分析显示携带GST-A1突变基因是6-TGN谷浓度升高的独立危险因素(低浓度水平OR=17.50,P=0.030;高浓度水平OR=3.60,P=0.033),而GST-M1、GST-P1、GST-T1基因多态性与6-TGN浓度水平无显著相关(P>0.05)。结论:GST-A1基因多态性可影响AZA活性代谢物6-TGN浓度水平,AZA治疗前进行GST-A1基因型检测将有助于临床个体化用药。

关键词: 炎症性肠病, 谷胱甘肽S转移酶基因多态性, 硫唑嘌呤, 6-硫鸟嘌呤核苷酸浓度

Abstract:

AIM: To investigate the effects of glutathione-S-transferase (GST) gene polymorphism on the concentration of 6-thioguanine nucleotides (6-TGN), an active metabolite of azathioprine (AZA), in patients with inflammatory bowel disease (IBD), in order to provide reference for the optimization of AZA treatment in patients. METHODS: The clinical data of patients with IBD treated by AZA were collected prospectively, the genotypes of GST-A1, GST-M1, GST-P1 and GST-T1 were detected by targeted sequencing of multiplex PCR combined with high-throughput sequencing technology before administration, and the steady-state trough concentrations of 6-TGN in patients' red blood cells were determined by HPLC. Statistical analysis was carried out by SPSS 26.0 software. RESULTS: A total of 90 patients were included in this study. The alleles frequencies of GST-A1, GST-M1, GST-P1 and GST-T1 were consistent with Hardy-Weinberg equilibrium law. Logistic regression analysis showed that carrying GST-A1 mutant gene was an independent risk factor for the increase of trough concentration of 6-TGN (low concentration OR=17.50, P=0.030; high concentration OR=3.60, P=0.033), while the gene polymorphism of GST-M1, GST-P1, GST-T1 had no significant correlation with the concentration of 6-TGN (P>0.05). CONCLUSION: The gene polymorphism of GST-A1 may affect the concentration of 6-TGN, an active metabolite of AZA, and detection of GST-A1 genotype before AZA treatment will contribute to clinical individualized medication.

Key words: inflammatory bowel disease, GST genetic polymorphism, azathioprine, 6-TGN concentration

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