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首页> 外文期刊>Journal of Crohn’s & colitis >Therapeutic drug monitoring of thiopurine metabolites in adult thiopurine tolerant IBD patients on maintenance therapy
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Therapeutic drug monitoring of thiopurine metabolites in adult thiopurine tolerant IBD patients on maintenance therapy

机译:成年耐受硫嘌呤的IBD患者中维持治疗的硫嘌呤代谢物的治疗药物监测

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Background and aims: Therapeutic drug monitoring of active metabolites of thiopurines, azathioprine and 6-mercaptopurine, is relatively new. The proposed therapeutic threshold level of the active 6-thioguanine nucleotides (6-TGN) is ≥235pmol/8×10 8 erythrocytes. The aim of this prospective cross-sectional study was to compare 6-TGN levels in adult thiopurine tolerant IBD patients with an exacerbation with those in remission, and to determine the therapeutic 6-TGN cut-off level. Methods: Hundred IBD patients were included. Outcome measures were thiopurine metabolite levels, calculated therapeutic 6-TGN cut-off level, CDAI/CAI scores, thiopurine dose and TPMT enzyme activity. Results: Forty-one patients had an exacerbation, 59 patients were in remission. In 17% of all patients 6-TGN levels were compatible with non-compliance. The median 6-TGN levels were not significantly different between the exacerbation and remission group (227 versus 263pmol/8×10 8 erythrocytes, p=0.29). The previous reported therapeutic 6-TGN cut-off level of 235pmol/8×10 8 erythrocytes was confirmed in this study. Twenty-six of the 41 patients (63%) with active disease had 6-TGN levels below this threshold and 24 of 59 IBD patients (41%) in clinical remission (p=0.04). Conclusions: Thiopurine non-compliance occurs frequently both in active and quiescent disease. 6-TGN levels below or above the therapeutic threshold are associated with a significant higher chance of IBD exacerbation and remission, respectively. These data support the role of therapeutic drug monitoring in thiopurine maintenance therapy in IBD to reveal non-compliance or underdosing, and can be used as a practical tool to optimize thiopurine therapy, especially in case of thiopurine non-response. .
机译:背景与目的:监测硫嘌呤,硫唑嘌呤和6-巯基嘌呤的活性代谢物的治疗药物相对较新。提议的活性6-硫鸟嘌呤核苷酸(6-TGN)的治疗阈值水平≥235pmol / 8×10 8红细胞。这项前瞻性横断面研究的目的是比较急性加重和缓解期加重的对硫代嘌呤耐受的成年IBD患者的6-TGN水平,并确定6-TGN的治疗临界水平。方法:纳入数百名IBD患者。结果指标为硫嘌呤代谢物水平,计算的6-TGN截断水平,CDAI / CAI评分,硫嘌呤剂量和TPMT酶活性。结果:41例病情加重,其中59例病情缓解。在所有患者中,有17%的6-TGN水平符合不依从标准。加重和缓解组之间的中位6-TGN水平无显着差异(227 vs 263pmol / 8×10 8红细胞,p = 0.29)。该研究证实了先前报道的235pmol / 8×10 8红细胞的治疗性6-TGN截止水平。 41例活动性疾病患者中有26例(63%)的6-TGN水平低于此阈值,59例IBD患者中有24例(41%)的临床缓解率(p = 0.04)。结论:硫嘌呤不合规在活动性和静止性疾病中都经常发生。低于或高于治疗阈值的6-TGN水平分别与IBD恶化和缓解的明显更高机会相关。这些数据支持治疗药物监测在IBD的硫嘌呤维持治疗中的作用,以揭示不合规或剂量不足,并且可以用作优化硫嘌呤治疗的实用工具,尤其是在硫嘌呤无反应的情况下。 。

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