首页> 外国专利> CRIM1 CRIM1 single nucleotide polymorphism marker in gene for predicting risk of drug induced leukopenia and method for predicting risk of drug induced leukopenia using the same

CRIM1 CRIM1 single nucleotide polymorphism marker in gene for predicting risk of drug induced leukopenia and method for predicting risk of drug induced leukopenia using the same

机译:CRIM1 CRIM1单核苷酸多态性标记基因,用于预测药物性白细胞减少症的风险以及使用该方法预测药物性白细胞减少症的方法

摘要

The present invention relates to a composition for predicting the risk of developing drug-induced leukopenia including a monobasic polymorphic marker in the CRIM1 gene and a method for predicting the risk of developing drug-induced leukopenia using the same. The single nucleotide polymorphism marker in the CRIM1 gene according to the present invention has a high correlation with the risk of leukopenia induced by drugs, in particular, chipurin-based drugs, and thus, leukemia, Crohn's disease, ulcerative colitis, or Customized patient who can effectively predict or diagnose patients with high susceptibility to leukopenia occurring during chemopurine-based drug treatment such as organ transplantation, and achieve optimal treatment effect by administering the appropriate drug to the patient Treatment can be performed efficiently. Furthermore, the monobasic polymorphic marker according to the present invention can be used in drug development studies for the treatment of drug-induced leukopenia.
机译:本发明涉及用于预测发生药物诱导的白细胞减少症的风险的组合物,其包括CRIM1基因中的一元多态性标记物,以及使用该组合物预测发生药物诱导的白细胞减少症的风险的方法。根据本发明的CRIM1基因中的单核苷酸多态性标志物与由药物,特别是基于奇尿林的药物引起的白细胞减少症的风险高度相关,因此与白血病,克罗恩氏病,溃疡性结肠炎或自定义患者可以有效地预测或诊断在基于化学嘌呤的药物治疗(例如器官移植)期间发生的对白细胞减少症高度敏感的患者,并通过向患者施用适当的药物达到最佳治疗效果。此外,根据本发明的一价多态性标记物可以用于药物开发研究中,以治疗药物诱导的白细胞减少症。

著录项

  • 公开/公告号KR20200083300A

    专利类型

  • 公开/公告日2020-07-08

    原文格式PDF

  • 申请/专利号KR20190175437

  • 发明设计人 김주한;

    申请日2019-12-26

  • 分类号C12Q1/6883;

  • 国家 KR

  • 入库时间 2022-08-21 11:06:28

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