首页> 外文期刊>Rheumatology international. >Invasive aspergillosis related with azathioprine-induced leucopenia without mutant allele of thioprine methyltransferase in a patient with rheumatoid arthritis.
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Invasive aspergillosis related with azathioprine-induced leucopenia without mutant allele of thioprine methyltransferase in a patient with rheumatoid arthritis.

机译:类风湿关节炎患者与硫唑嘌呤诱导的白细胞减少症相关的侵袭性曲霉病,而无硫嘌呤甲基转移酶突变等位基因。

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摘要

Azathioprine (AZA) may induce bone marrow suppression, especially leucopenia. AZA-induced leucopenia is caused by excessive accumulation of intracellular 6-thioguanine nucleotides (6-TGN) during AZA metabolism [1]. This abnormality is often associated with mutations of enzyme thioprine methyltransferase (TPMT) gene, which catalyzes S-methylation of AZA. Severe leucopenia is estimated to occur in about 3% of cases of AZA treatment for rheumatoid arthritis (RA) and is often life threatening in this context [2]. The overall incidence of adverse reactions to AZA is relatively high, even in patients with the wild-type TPMT genotype [3].
机译:硫唑嘌呤(AZA)可能诱导骨髓抑制,尤其是白细胞减少症。 AZA引起的白细胞减少症是由AZA代谢过程中细胞内6-硫鸟嘌呤核苷酸(6-TGN)的过度积累引起的[1]。这种异常现象通常与硫代嘌呤甲基转移酶(TPMT)基因突变有关,该基因催化AZA的S-甲基化。据估计,约有3%的AZA治疗类风湿关节炎(RA)会发生严重的白细胞减少症,并且在这种情况下通常会危及生命[2]。即使是野生型TPMT基因型的患者,对AZA不良反应的总发生率也相对较高[3]。

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