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评估在接受硫嘌呤治疗的儿童中使用代谢产物测量的情况。

Evaluating the use of metabolite measurement in children receiving treatment with a thiopurine.

机构信息

Department of Gastroenterology, Hepatology and Nutrition, Royal Hospital for Sick Children, Glasgow, UK.

出版信息

Aliment Pharmacol Ther. 2011 Nov;34(9):1106-14. doi: 10.1111/j.1365-2036.2011.04848.x. Epub 2011 Sep 19.

Abstract

BACKGROUND

Clinical response to thiopurine medication is related to the concentration of its metabolites. Proxy measures are traditionally used to assess dose adequacy. We present our experience of using tioguanine (previously known/formerly referred to as thioguanine) metabolite measurements in paediatric patients and evaluate their effect on clinical practice.

AIMS

To report our experience of using tioguanine metabolite measurements in paediatric patients and to evaluate their effects on clinical practice.

METHODS

The 6-tioguanine nucleotide (6-TGN) and 6-methylmercaptopurine (6-MMP) were measured in children prescribed thiopurine medication for at least 3 months. Data were collected on thiopurine methyl transferase (TPMT) genotype, drug dose, laboratory indices and management changes. Therapeutic 6-TGN levels were defined as 235-400 pmol/8 × 10(8) RBCs. Seventy individuals (30 males) with a median age of 15 years. Underlying diagnoses were 'IBD' (68/70) and two cases of eosinophilic colitis. Sixty-three were treated with azathioprine and seven with mercaptopurine. A total of 103 separate measurements were made.

RESULTS

On initial measurement, 68% of patients had 6-TGN levels outside therapeutic levels despite standard thiopurine dosing. Initial 6-TGN levels were significantly higher in patients with TPMT mutations. Toxicity occurred in seven cases. The 6-TGN levels were significantly higher in those with signs of marrow toxicity. The 6-TGN level correlated with WBC, leukocyte count, mean corpuscular volume (MCV) and ΔMCV; however, the ability of each of these to predict therapeutic 6-TGN levels was poor. After initial measurement, management was changed in 25/70 cases (36%).

CONCLUSIONS

6-TGN levels were therapeutic in a minority of those patients who were tested. Proxy measures perform poorly in predicting therapeutic 6-TGN levels. Measuring thiopurine metabolites is useful for dosage adjustment in children, and for the detection of potential toxicity.

摘要

背景

硫嘌呤类药物的临床反应与代谢物浓度有关。传统上使用替代指标来评估剂量是否充足。我们介绍了在儿科患者中使用硫鸟嘌呤(以前称为硫鸟嘌呤)代谢物测量的经验,并评估了它们对临床实践的影响。

目的

报告我们在儿科患者中使用硫鸟嘌呤代谢物测量的经验,并评估它们对临床实践的影响。

方法

对至少服用硫嘌呤药物 3 个月的儿童进行 6-硫鸟嘌呤核苷酸(6-TGN)和 6-甲基巯基嘌呤(6-MMP)测量。收集硫嘌呤甲基转移酶(TPMT)基因型、药物剂量、实验室指标和管理变化的数据。治疗性 6-TGN 水平定义为 235-400 pmol/8×10(8)RBC。70 名个体(30 名男性)的中位年龄为 15 岁。基础诊断为“炎症性肠病”(68/70)和 2 例嗜酸性结肠炎。63 例接受硫唑嘌呤治疗,7 例接受巯嘌呤治疗。共进行了 103 次单独测量。

结果

尽管标准的硫嘌呤剂量,但初始测量时,68%的患者 6-TGN 水平不在治疗范围内。TPMT 突变患者的初始 6-TGN 水平明显更高。7 例发生毒性。骨髓毒性迹象的患者 6-TGN 水平明显更高。6-TGN 水平与白细胞计数、白细胞计数、平均红细胞体积(MCV)和ΔMCV 相关;然而,这些指标预测治疗性 6-TGN 水平的能力都很差。初始测量后,70 例患者中有 25 例(36%)改变了治疗方案。

结论

在接受检测的患者中,少数患者的 6-TGN 水平处于治疗范围内。替代指标预测治疗性 6-TGN 水平的效果不佳。测量硫嘌呤代谢物有助于儿童调整剂量,并检测潜在毒性。

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