Exposure to Azathioprine Metabolites and Clinical Outcome in Indian Patients with Crohn’s Disease

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2022-03-24 DOI:10.1177/0976500X221085804
R. Prabha, Sumith K. Mathew, A. Joseph, B. Mathew
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引用次数: 1

Abstract

Aim: To determine the concentration of 6-thioguanine nucleotide (6-TGN) and 6-methylmercaptopurine (6-MMP), the interpatient variability, and the relationship with disease activity in patients with Chron’s disease on long-term stable doses of azathioprine (AZA). Methods: This is a prospective, tertiary care single-center hospital study in adult Chron’s disease patients treated with AZA. The quantification of phenotypic thiopurine methyltransferase enzyme activity in red blood cells and the estimation of the concentration of 6-TGN and 6-MMP in whole blood was performed using the HPLC-UV detector method. A clinical response was categorized as remission (Harvey-Bradshaw Index [HBI] < 5) or improvement (drop from baseline of at least three points of HBI) based on HBI. Exposure to metabolite concentrations and the clinical response to AZA treatment was observed. Results: Study analysis included 30 patients who were initiated on AZA, and they were followed up with an estimation of metabolite concentrations to determine their clinical outcome. At six months, 93% of (n = 28) patients continued to be on AZA and had clinical improvement. All the patients achieved remission of Chron’s disease. Only two patients developed adverse effects such as joint pain and thrombocytopenia. Conclusion: AZA is a safe and effective therapy in managing Chron’s disease when administered after determining thiopurine methyltransferase phenotype and with dose optimization performed using therapeutic drug monitoring of 6-TGN and 6-MMP.
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印度克罗恩病患者硫嘌呤代谢产物的暴露与临床结果
目的:测定长期稳定剂量的硫唑嘌呤(AZA)对慢性病患者6-硫鸟嘌呤核苷酸(6-TGN)和6-甲基巯基嘌呤(6-MMP)的浓度、患者间变异性以及与疾病活动性的关系。方法:这是一项前瞻性的三级护理单中心医院研究,研究对象为接受AZA治疗的成年慢性病患者。使用HPLC-UV检测器法对红细胞中表型硫嘌呤甲基转移酶活性进行定量,并估计全血中6-TGN和6-MMP的浓度。根据HBI,临床反应分为缓解(Harvey-Bradshaw指数[HBI]<5)或改善(HBI从基线下降至少三分)。观察到暴露于代谢物浓度和对AZA治疗的临床反应。结果:研究分析包括30名开始服用AZA的患者,并对他们进行了代谢产物浓度估计,以确定他们的临床结果。6个月时,93%(n=28)的患者继续接受AZA治疗,并有临床改善。所有患者均获得了克龙病的缓解。只有两名患者出现了关节疼痛和血小板减少等不良反应。结论:在确定硫嘌呤甲基转移酶表型后给予AZA,并使用6-TGN和6-MMP的治疗药物监测进行剂量优化,AZA是一种安全有效的治疗慢性病的方法。
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