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在日本炎症性肠病患者中,NUDT15 R139C相关的硫嘌呤白细胞减少症是由6-硫鸟嘌呤核苷酸非依赖性机制介导的。

NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease.

作者信息

Asada Ayumi, Nishida Atsushi, Shioya Makoto, Imaeda Hirotsugu, Inatomi Osamu, Bamba Shigeki, Kito Katsuyuki, Sugimoto Mitsushige, Andoh Akira

机构信息

Department of Medicine, Shiga University of Medical Science, Seta-Tukinowa, Otsu, 520-2192, Japan.

出版信息

J Gastroenterol. 2016 Jan;51(1):22-9. doi: 10.1007/s00535-015-1142-4. Epub 2015 Nov 21.

Abstract

BACKGROUND

NUDT15 R139C (rs116855232) is a recently identified genetic factor responsible for thiopurine-induced leukocytopenia and hair loss. In this study, we investigated the association of NUDT15 R139C with 6-thioguanine nucleotide (6-TGN) levels and thiopurine-induced leukocytopenia in Japanese patients with inflammatory bowel disease (IBD).

METHODS

Two hundred and sixty-four subjects (103 healthy volunteers and 161 IBD patients treated with thiopurines) were enrolled. Genotyping for NUDT15 R139C was performed using Custom TaqMan® SNP genotyping assays.

RESULTS

The NUDT15 C/C, C/T, and T/T genotypes were 80.7, 18.2, and 1.1 %, respectively. The allelic frequency was 10.2 %. Among 161 IBD patients, there was no significant difference in 6-TGN levels among the NUDT15 genotypes. Forty-five patients (27.9 %) developed leukocytopenia (WBC <3000/μl), and the C/T and T/T genotypes were significantly associated with the development of leukocytopenia (P = 1.7 × 10(-5)). In these patients, 6-TGN levels were not significantly different between NUDT15 genotypes. NUDT15 R139C was significantly associated with early (<8 weeks) (P = 1.03 × 10(-4)) and late (>8 weeks) leukocytopenia (P = 4.3 × 10(-4)). The decrease in WBC count at 2 and 4 weeks was significantly higher in patients with the C/T or T/T genotypes as compared to the patients with the C/C genotype. All patients with the T/T genotype (n = 2) developed early severe hair loss and severe leukocytopenia (<1000/μl). The logistic regression analysis revealed that NUDT15 R139C was the sole genetic factor responsible for the thiopurine-induced leukocytopenia (P = 0.001).

CONCLUSIONS

These results suggest that NUDT15 R139C-related thiopurine-induced leukocytopenia is mediated by a 6-TGN-independent mechanism.

摘要

背景

NUDT15 R139C(rs116855232)是最近发现的一种导致硫嘌呤引起白细胞减少和脱发的遗传因素。在本研究中,我们调查了日本炎症性肠病(IBD)患者中NUDT15 R139C与6-硫鸟嘌呤核苷酸(6-TGN)水平及硫嘌呤诱导的白细胞减少之间的关联。

方法

纳入264名受试者(103名健康志愿者和161名接受硫嘌呤治疗的IBD患者)。使用定制TaqMan®SNP基因分型检测法对NUDT15 R139C进行基因分型。

结果

NUDT15 C/C、C/T和T/T基因型分别为80.7%、18.2%和1.1%。等位基因频率为10.2%。在161名IBD患者中,NUDT15各基因型的6-TGN水平无显著差异。45名患者(27.9%)发生白细胞减少(白细胞计数<3000/μl),C/T和T/T基因型与白细胞减少的发生显著相关(P = 1.7×10⁻⁵)。在这些患者中,NUDT15各基因型的6-TGN水平无显著差异。NUDT15 R139C与早期(<8周)(P = 1.03×10⁻⁴)和晚期(>8周)白细胞减少显著相关(P = 4.3×10⁻⁴)。与C/C基因型患者相比,C/T或T/T基因型患者在第2周和第4周时白细胞计数的下降幅度显著更大。所有T/T基因型患者(n = 2)均出现早期严重脱发和严重白细胞减少(<1000/μl)。逻辑回归分析显示,NUDT15 R139C是硫嘌呤诱导白细胞减少的唯一遗传因素(P = 0.001)。

结论

这些结果表明,NUDT15 R139C相关的硫嘌呤诱导白细胞减少是由一种不依赖6-TGN的机制介导的。

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