Asada Ayumi, Nishida Atsushi, Shioya Makoto, Imaeda Hirotsugu, Inatomi Osamu, Bamba Shigeki, Kito Katsuyuki, Sugimoto Mitsushige, Andoh Akira
Department of Medicine, Shiga University of Medical Science, Seta-Tukinowa, Otsu, 520-2192, Japan.
J Gastroenterol. 2016 Jan;51(1):22-9. doi: 10.1007/s00535-015-1142-4. Epub 2015 Nov 21.
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).
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.
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).
These results suggest that NUDT15 R139C-related thiopurine-induced leukocytopenia is mediated by a 6-TGN-independent mechanism.
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。
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。
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)。
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。