首页> 美国卫生研究院文献>The Journal of Pediatric Pharmacology and Therapeutics : JPPT >Association Between Thiopurine S-Methyltransferase (TPMT) Genetic Variants and Infection in Pediatric Heart Transplant Recipients Treated With Azathioprine: A Multi-Institutional Analysis
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Association Between Thiopurine S-Methyltransferase (TPMT) Genetic Variants and Infection in Pediatric Heart Transplant Recipients Treated With Azathioprine: A Multi-Institutional Analysis

机译:硫硫嘌呤治疗硫嘌呤S-甲基转移酶(TPMT)遗传变异与小儿心脏移植受者感染之间的关联:多机构分析

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摘要

OBJECTIVESBone marrow suppression is a common adverse effect of the immunosuppressive drug azathioprine. Polymorphisms in the gene encoding thiopurine S-methyltransferase (TPMT) can alter the metabolism of azathioprine, resulting in marrow toxicity and life-threatening infection. In a multicenter cohort of pediatric heart transplant (HT) recipients, we determined the frequency of TPMT genetic variation and assessed whether azathioprine-treated recipients with TPMT variants were at increased risk of infection.
机译:目的骨髓抑制是免疫抑制药物硫唑嘌呤的常见不良反应。编码硫嘌呤S-甲基转移酶(TPMT)的基因中的多态性可以改变硫唑嘌呤的代谢,从而导致骨髓毒性和威胁生命的感染。在多中心儿科心脏移植(HT)接受者队列中,我们确定了TPMT遗传变异的频率,并评估了硫唑嘌呤治疗的TPMT变异接受者是否有增加的感染风险。

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