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核苷酸多态性 c.415C>T(精氨酸 139 胱氨酸)和 c.416G>A(精氨酸 139 组氨酸)与 NUDT15 基因相关,可导致巯嘌呤诱导的白细胞减少症。

Single-Nucleotide Polymorphisms, c.415C > T (Arg139Cys) and c.416G > A (Arg139His), in the NUDT15 Gene Are Associated with Thiopurine-Induced Leukopenia.

机构信息

Department of Pharmacy, Shiga University of Medical Science Hospital.

Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital.

出版信息

Biol Pharm Bull. 2023;46(3):412-418. doi: 10.1248/bpb.b22-00686.

DOI:10.1248/bpb.b22-00686
PMID:36858569
Abstract

While nucleoside diphosphate-linked moiety X-type motif 15 (NUDT15) gene polymorphism Arg139Cys (rs116855232) is known to be a risk factor for thiopurine-induced severe leukopenia, association with the NUDT15 gene polymorphism Arg139His (rs147390019) has not yet been clarified. In addition, the accuracy of TaqMan PCR to assess these two polymorphisms has not been investigated. In this study, we evaluated TaqMan PCR for detection of the NUDT15 single-nucleotide polymorphisms (SNPs) and examined the clinical impact of Arg139His on thiopurine-induced leukopenia. First, we demonstrated that a TaqMan PCR assay successfully detected the Arg139His polymorphism of NUDT15 in clinical samples. Next, the NUDT15 gene polymorphisms (Arg139Cys and Arg139His) were separately analyzed by TaqMan Real-Time PCR in 189 patients from August 2018 to July 2019. The incidences of leukopenia within 2 years were 16.2, 57.9, and 100% for arginine (Arg)/Arg, Arg/cysteine (Cys), and Arg/histidine (His), respectively. The leukopenia was significantly increased in Arg/Cys and Arg/His compared with Arg/Arg. This retrospective clinical study indicated that, in addition to Arg139Cys, Arg139His may be clinically associated with a high risk of leukopenia. Pharmacogenomics will help in selecting drugs and determining the individualized dosage of thiopurine drugs.

摘要

核苷酸二磷酸连接的部分 X 基序 15(NUDT15)基因多态性 Arg139Cys(rs116855232)已知是硫嘌呤诱导严重白细胞减少症的风险因素,但与 NUDT15 基因多态性 Arg139His(rs147390019)的关联尚未阐明。此外,TaqMan PCR 评估这些两种多态性的准确性尚未得到研究。在这项研究中,我们评估了 TaqMan PCR 检测 NUDT15 单核苷酸多态性(SNP)的能力,并研究了 Arg139His 对硫嘌呤诱导的白细胞减少症的临床影响。首先,我们证明 TaqMan PCR 检测可成功检测临床样本中的 NUDT15 Arg139His 多态性。接下来,我们于 2018 年 8 月至 2019 年 7 月,通过 TaqMan Real-Time PCR 分别分析了 189 例患者的 NUDT15 基因多态性(Arg139Cys 和 Arg139His)。Arg/Arg、Arg/Cys 和 Arg/His 基因型的患者在 2 年内发生白细胞减少症的比例分别为 16.2%、57.9%和 100%。与 Arg/Arg 相比,Arg/Cys 和 Arg/His 基因型的白细胞减少症显著增加。这项回顾性临床研究表明,除 Arg139Cys 外,Arg139His 可能与白细胞减少症的高风险具有临床相关性。药物基因组学有助于选择药物和确定硫嘌呤类药物的个体化剂量。

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