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The pharmacokinetic effect of adalimumab on thiopurine metabolism in Crohn's disease patients

机译:阿达木单抗对克罗恩病患者硫嘌呤代谢的药代动力学作用

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Background and aims: A drug interaction between infliximab and azathioprine has previously been reported in Crohn's disease patients: the concentration of the main active thiopurine metabolites, the 6-thioguanine nucleotides (6-TGN), increased 1-3. weeks after the first infliximab infusion by 50% compared to baseline. The aim of this prospective study was to determine the effect of adalimumab on thiopurine metabolism in Crohn's disease patients, evaluated by 6-TGN and 6-methylmercaptopurine ribonucleotides (6-MMPR) concentration measurement. Methods: Crohn's disease patients on azathioprine or mercaptopurine maintenance therapy starting with concomitant adalimumab treatment were included. 6-TGN and 6-MMPR concentrations were determined before initiation of adalimumab and after 2, 4, 6 and 12. weeks of combination therapy. The activity of three essential enzymes involving thiopurine metabolism, thiopurine S-methyltransferase (TPMT), hypoxanthine-guanine phosphoribosyl transferase (HGPRT) and inosine-triphosphate pyrophosphatase (ITPase), was evaluated at baseline and week 4. Clinical outcome was evaluated by the Crohn's disease activity index and C-reactive protein concentrations at baseline, week 4 and week 12. Results: Twelve Crohn's disease patients were analyzed. During the follow-up period of 12. weeks the median 6-TGN and 6-MMPR concentrations did not significantly change compared to baseline. TPMT, ITPase and HGPRT enzyme activity did not change either after 4. weeks. In two patients (17%) myelotoxicity was observed within 2-4. weeks, in whom both low therapeutic 6-TGN and 6-MMPR concentrations were found. Conclusions: In this study in Crohn's disease patients no pharmacokinetic interaction was shown between adalimumab and the conventional thiopurines, azathioprine and mercaptopurine.
机译:背景与目的:以前在克罗恩病患者中已有英夫利昔单抗和硫唑嘌呤之间的药物相互作用的报道:主要的活性硫嘌呤代谢产物6-硫鸟嘌呤核苷酸(6-TGN)的浓度增加了1-3。与基线相比,首次英夫利昔单抗输注后数周减少了50%。这项前瞻性研究的目的是确定阿达木单抗对克罗恩病患者硫代嘌呤代谢的影响,通过6-TGN和6-甲基巯基嘌呤核糖核苷酸(6-MMPR)浓度测量进行评估。方法:包括接受硫唑嘌呤或巯基嘌呤维持治疗并开始阿达木单抗治疗的克罗恩病患者。在开始阿达木单抗之前和联合治疗的2、4、6和12周后确定6-TGN和6-MMPR浓度。在基线和第4周评估了涉及硫嘌呤代谢的三种基本酶的活性:硫嘌呤S-甲基转移酶(TPMT),次黄嘌呤-鸟嘌呤磷酸核糖基转移酶(HGPRT)和肌苷-三磷酸焦磷酸酶(ITPase)。基线,第4周和第12周时的疾病活动指数和C反应蛋白浓度。结果:分析了12名克罗恩病患者。在12周的随访期内,中位6-TGN和6-MMPR浓度与基线相比无明显变化。 TPMT,ITPase和HGPRT酶活性在4周后均未改变。在2例患者中(17%)在2-4内观察到骨髓毒性。数周后,发现6-TGN和6-MMPR的治疗浓度均较低。结论:在这项针对克罗恩病患者的研究中,未显示阿达木单抗与常规硫代嘌呤,硫唑嘌呤和巯基嘌呤之间存在药代动力学相互作用。

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