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成人巯嘌呤耐受的 IBD 患者在维持治疗时硫嘌呤代谢物的治疗药物监测。

Therapeutic drug monitoring of thiopurine metabolites in adult thiopurine tolerant IBD patients on maintenance therapy.

机构信息

Department of Gastroenterology and Hepatology, Catharina Hospital, Eindhoven, The Netherlands.

出版信息

J Crohns Colitis. 2012 Jul;6(6):698-707. doi: 10.1016/j.crohns.2011.12.003. Epub 2012 Jan 10.

Abstract

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 ≥235 pmol/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 263 pmol/8×10(8) erythrocytes, p=0.29). The previous reported therapeutic 6-TGN cut-off level of 235 pmol/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.

摘要

背景与目的

硫嘌呤类药物(巯嘌呤和 6-巯基嘌呤)的活性代谢产物的治疗药物监测相对较新。建议的活性 6-硫鸟嘌呤核苷酸(6-TGN)治疗阈值水平为≥235 pmol/8×10(8)红细胞。本前瞻性横断面研究的目的是比较处于缓解期和活动期的硫嘌呤耐受的 IBD 患者的 6-TGN 水平,并确定治疗性 6-TGN 截止值。

方法

纳入 100 例 IBD 患者。观察指标为硫嘌呤代谢产物水平、计算的治疗性 6-TGN 截止值、CDAI/CAI 评分、硫嘌呤剂量和 TPMT 酶活性。

结果

41 例患者病情加重,59 例患者缓解。在所有患者中,有 17%的患者 6-TGN 水平与不依从有关。活动期和缓解期患者的 6-TGN 中位数无显著差异(227 与 263 pmol/8×10(8)红细胞,p=0.29)。本研究证实了之前报道的 235 pmol/8×10(8)红细胞的治疗性 6-TGN 截止值。41 例活动期疾病患者中有 26 例(63%)的 6-TGN 水平低于该阈值,59 例 IBD 患者中有 24 例(41%)处于临床缓解期(p=0.04)。

结论

硫嘌呤不依从在活动期和缓解期疾病中均频繁发生。低于或高于治疗阈值的 6-TGN 水平与 IBD 加重和缓解的几率显著增加相关。这些数据支持在 IBD 的硫嘌呤维持治疗中进行治疗药物监测以发现不依从或剂量不足,并可作为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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