首页> 外文期刊>Therapeutic Drug Monitoring >Monitoring of thiopurine methyltransferase activity in postsurgical patients with Crohn's disease during 1 year of treatment with azathioprine or mesalazine.
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Monitoring of thiopurine methyltransferase activity in postsurgical patients with Crohn's disease during 1 year of treatment with azathioprine or mesalazine.

机译:硫唑嘌呤或美沙拉嗪治疗1年后克罗恩病术后患者的硫嘌呤甲基转移酶活性的监测。

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Thiopurine methyltransferase (TPMT) activity determines biotransformation of azathioprine and, thereby, drug efficacy and safety. Evaluation of a possible long-term effect of mesalazine or azathioprine on TPMT activity is of particular clinical importance because both drugs can to be given for several years in inflammatory bowel disease. Monitoring of TPMT activity and three thiopurine metabolites was performed prospectively during a 1 year postoperative period in 21 patients with Crohn's disease randomly assigned to azathioprine (2.0-2.5 mg/kg per day) or mesalazine (4 g/day). TPMT activity did not change significantly within each treatment group during 52 weeks. At any study visit, TPMT activity was not different between 13 patients on azathioprine and eight patients on mesalazine. Concentrations of 6-thioguanine nucleotides (6-TGN, active moiety of azathioprine) and 6-methyl-mercaptopurine ribonucleotides (6-MMPR) did not alter significantly during the observation period, except for a slight decrease in 6-TGN levels when comparing the first with the last visit. In this first report of serial monitoring of 6-methyl-thioguanine nucleotides (6-MTGN) in patients with inflammatory bowel disease taking azathioprine, high levels of 6-TGN were correlated with high levels of 6-MTGN, with the mean 6-TGN:6-MTGN ratio being 2.4. In a well-standardized clinical setting of inflammatory bowel disease, neither mesalazine nor azathioprine significantly affected TPMT activity during a whole year of treatment.
机译:硫嘌呤甲基转移酶(TPMT)的活性决定了硫唑嘌呤的生物转化,从而决定了药物的效力和安全性。评估美沙拉嗪或硫唑嘌呤对TPMT活性的可能的长期影响具有特殊的临床意义,因为这两种药物均可在炎症性肠病中使用数年。在21名患有克罗恩病的患者中,随机分配了硫唑嘌呤(2.0-2.5 mg / kg /天)或美沙拉嗪(4 g /天),对术后1年内的TPMT活性和三种硫嘌呤代谢产物进行了监测。在52周内,每个治疗组中TPMT活性均无明显变化。在任何研究访视中,硫唑嘌呤的13例患者和美沙拉嗪的8例患者的TPMT活性没有差异。在观察期间,6-硫鸟嘌呤核苷酸(6-TGN,硫唑嘌呤的活性部分)和6-甲基-巯嘌呤核糖核苷酸(6-MMPR)的浓度没有显着变化,但6-TGN含量在比较时略有下降。首先是最后一次访问。在第一个连续监测服用硫唑嘌呤的炎性肠病患者中6-甲基-硫鸟嘌呤核苷酸(6-MTGN)的报告中,高水平的6-TGN与高水平的6-MTGN相关,平均值为6-TGN :6-MTGN比为2.4。在炎症性肠病的标准化临床环境中,美沙拉嗪和硫唑嘌呤在整个治疗过程中均未显着影响TPMT活性。

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