Department of Clinical Pharmacy & Toxicology, Orbis Medical Centre, Sittard, The Netherlands.
Department of Gastroenterology and Hepatology, University Hospital Maastricht, Maastricht, The Netherlands.
J Crohns Colitis. 2014 Feb;8(2):120-8. doi: 10.1016/j.crohns.2013.07.004. Epub 2013 Aug 7.
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.
背景与目的:先前有报道称,在克罗恩病患者中,英夫利昔单抗与硫唑嘌呤之间存在药物相互作用:与基线相比,首次输注英夫利昔单抗后 1-3 周,主要活性硫嘌呤代谢物 6-硫鸟嘌呤核苷酸(6-TGN)的浓度增加了 50%。本前瞻性研究的目的是通过测定 6-TGN 和 6-甲基巯基嘌呤核糖核苷酸(6-MMPR)浓度来确定阿达木单抗对克罗恩病患者硫嘌呤代谢的影响。
方法:纳入开始接受阿达木单抗联合治疗的同时接受硫唑嘌呤或巯嘌呤维持治疗的克罗恩病患者。在开始阿达木单抗治疗之前以及联合治疗 2、4、6 和 12 周后,测定 6-TGN 和 6-MMPR 浓度。在基线和第 4 周评估参与硫嘌呤代谢的三种必需酶的活性,即硫嘌呤 S-甲基转移酶(TPMT)、次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HGPRT)和肌苷三磷酸焦磷酸酶(ITPase)。在基线、第 4 周和第 12 周通过克罗恩病活动指数和 C-反应蛋白浓度评估临床疗效。
结果:分析了 12 例克罗恩病患者。在 12 周的随访期间,与基线相比,6-TGN 和 6-MMPR 浓度的中位数没有显著变化。4 周后,TPMT、ITPase 和 HGPRT 酶活性也没有变化。在 2 名患者(17%)中,在 2-4 周内观察到骨髓毒性,在这两名患者中均发现治疗性 6-TGN 和 6-MMPR 浓度较低。
结论:在这项克罗恩病患者的研究中,阿达木单抗与传统的硫嘌呤(硫唑嘌呤和巯嘌呤)之间未显示出药代动力学相互作用。
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