首页> 外文期刊>Digestive and liver disease: official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver >Thiopurine methyltransferase activity combined with 6-thioguanine metabolite levels predicts clinical response to thiopurines in patients with inflammatory bowel disease.
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Thiopurine methyltransferase activity combined with 6-thioguanine metabolite levels predicts clinical response to thiopurines in patients with inflammatory bowel disease.

机译:硫嘌呤甲基转移酶活性与6-硫鸟嘌呤代谢产物水平相结合,可预测炎症性肠病患者对硫嘌呤的临床反应。

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BACKGROUND/AIMS: 6-Mercaptopurine and its prodrug azathioprine are effective for the treatment of inflammatory bowel disease. Thiopurine methyltransferase is important for the metabolism of thiopurines. However, there is controversy as to the clinical utility of measuring thiopurine methyltransferase enzyme activity and 6-thioguanine nucleotide levels. Our aim was to determine if thiopurine methyltransferase enzyme activity and 6-thioguanine nucleotide level monitoring would predict response to therapy with thiopurines in patients with inflammatory bowel disease. METHODS: Baseline thiopurine methyltransferase enzyme activity prior to initiation of therapy with either 6-mercaptopurine or azathioprine was determined in 39 patients with inflammatory bowel disease. The association between clinical response and thiopurine methyltransferase activity and 6-thioguanine nucleotide levels singly or in combination were analysed. RESULTS: Seventeen of 39 patients (44%) responded to 6-mercaptopurine or azathioprinetherapy. Thiopurine methyltransferase enzyme activity below the mean of 30.5 U was significantly associated with clinical response. The thiopurine methyltransferase low phenotype was associated with response in 65% vs. 29% in individuals with thiopurine methyltransferase enzyme activity above 30.5 U (p = 0.05). There was no correlation between thiopurine methyltransferase activity and 6-thioguanine nucleotide levels. The maximal 6-thioguanine nucleotide levels did not predict clinical response. When combining thiopurine methyltransferase enzyme activity and 6-thioguanine nucleotide levels, the combination of thiopurine methyltransferase low/6-thioguanine nucleotide high was associated with response in 7/7 (100%) vs. only 2/8 (25%) with the combination of thiopurine methyltransferase high/6-thioguanine nucleotide low (p=0.01). CONCLUSIONS: Thiopurine methyltransferase activity inversely correlated with clinical response to thiopurine treatment in inflammatory bowel disease. Thiopurine methyltransferase enzyme activity below 30.5 U combined with a post-treatment 6-thioguanine nucleotide level > 230 pmol/8 x 10(8) erythrocytes was the best predictor of response.
机译:背景/目的:6-巯基嘌呤及其前药硫唑嘌呤可有效治疗炎性肠病。硫嘌呤甲基转移酶对于硫嘌呤的代谢很重要。然而,关于测量硫嘌呤甲基转移酶活性和6-硫鸟嘌呤核苷酸水平的临床实用性存在争议。我们的目的是确定在炎症性肠病患者中,硫嘌呤甲基转移酶活性和6-硫鸟嘌呤核苷酸水平监测是否可以预测对硫嘌呤治疗的反应。方法:对39例炎症性肠病患者中的6-巯基嘌呤或硫唑嘌呤开始治疗之前,先测定基线硫嘌呤甲基转移酶的活性。单独或联合分析了临床反应与硫嘌呤甲基转移酶活性和6-硫鸟嘌呤核苷酸水平之间的关联。结果:39例患者中有17例(44%)对6-巯基嘌呤或硫唑嘌呤疗法有反应。硫嘌呤甲基转移酶活性低于平均值30.5 U与临床反应显着相关。硫嘌呤甲基转移酶活性低的表型与65%的应答率相关,而硫嘌呤甲基转移酶活性高于30.5 U的个体的应答率为29%(p = 0.05)。硫嘌呤甲基转移酶活性与6-硫鸟嘌呤核苷酸水平之间没有相关性。最大的6-硫鸟嘌呤核苷酸水平不能预测临床反应。当结合硫嘌呤甲基转移酶活性和6-硫鸟嘌呤核苷酸水平时,硫嘌呤甲基转移酶低/ 6-硫鸟嘌呤核苷酸高的组合与响应的相关性为7/7(100%),而组合仅为2/8(25%)硫嘌呤甲基转移酶高/ 6硫代鸟嘌呤核苷酸低(p = 0.01)。结论:硫嘌呤甲基转移酶活性与炎性肠病中对硫嘌呤治疗的临床反应呈负相关。低于30.5 U的硫嘌呤甲基转移酶活性与治疗后的6-硫鸟嘌呤核苷酸水平> 230 pmol / 8 x 10(8)红细胞相结合,是反应的最佳预测指标。

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