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首页> 外文期刊>Inflammatory bowel diseases >Relationship Between Azathioprine Dosage, 6-Thioguanine Nucleotide Levels, and Therapeutic Response in Pediatric Patients with IBD Treated with Azathioprine
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Relationship Between Azathioprine Dosage, 6-Thioguanine Nucleotide Levels, and Therapeutic Response in Pediatric Patients with IBD Treated with Azathioprine

机译:硫唑嘌呤治疗的IBD患儿的硫唑嘌呤剂量,6-硫鸟嘌呤核苷酸水平与治疗反应之间的关系

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Background:Azathioprine (AZA) is commonly used to treat IBD either alone or in combination with mesalazine. However, there are relatively few studies concerning the relationship between AZA dose, thiopurine metabolite levels, and therapeutic response in pediatric patients treated with both AZA and mesalazine.Methods:We retrospectively investigated the relationship between AZA dose, thiopurine metabolite levels, and therapeutic response in 137 pediatric patients with IBD treated with AZA using multilevel analysis. Additional factors affecting metabolite levels and therapeutic response were also analyzed.Results:A positive correlation was observed between AZA dosage and 6-thioguanine nucleotide (6-TGN) level (P < 0.0001). Variant TPMT genotype (P < 0.001) and concomitant use of mesalazine (P < 0.001) were predictors of higher 6-TGN levels. Leukopenia (P = 0.025) and lymphopenia (P = 0.045) were associated with higher levels of 6-TGN. Poor AZA compliance affected median 6-TGN levels (P < 0.001). The frequency of patients with median 6-TGN levels >235 pmol per 8 x 10(8) red blood cells was the highest in the sustained therapeutic response group (P = 0.015). Age, sex, IBD type, and duration of AZA therapy did not influence 6-TGN levels or therapeutic effect.Conclusions:AZA dosage is positively correlated with 6-TGN level. Higher 6-TGN levels are related to leukopenia, lymphopenia, and concurrent use of mesalazine. These results provide the rationale for monitoring metabolites to optimize drug dosing and minimize drug-related toxicity. In addition, maintenance of 6-TGN levels within a beneficial therapeutic range by direct monitoring should be helpful in attaining therapeutic efficacy, although this possibility should be verified in prospective studies.
机译:背景:硫唑嘌呤(AZA)通常用于单独或与美沙拉嗪联用治疗IBD。然而,关于AZA剂量,硫代嘌呤代谢物水平与美沙拉嗪同时治疗的儿科患者的治疗反应之间关系的研究相对较少。方法:我们回顾性研究了AZA剂量,硫代嘌呤代谢物水平与治疗患者之间的关系。使用多级分析对137例IZA治疗的IBD小儿患者。结果:AZA剂量与6-硫鸟嘌呤核苷酸(6-TGN)水平呈正相关(P <0.0001)。 TPMT基因型的差异(P <0.001)和美沙拉嗪的同时使用(P <0.001)是6-TGN水平升高的预测指标。白细胞减少症(P = 0.025)和淋巴细胞减少症(P = 0.045)与6-TGN升高相关。 AZA依从性差会影响6-TGN的中位数水平(P <0.001)。在持续治疗反应组中,6-TGN中位数水平> 235 pmol / 8 x 10(8)红细胞的患者频率最高(P = 0.015)。年龄,性别,IBD类型和AZA治疗持续时间均不影响6-TGN水平或疗效。结论:AZA剂量与6-TGN水平呈正相关。较高的6-TGN水平与白细胞减少症,淋巴细胞减少症和美沙拉嗪的同时使用有关。这些结果提供了监测代谢物以优化药物剂量并使药物相关毒性最小化的理由。另外,通过直接监测将6-TGN水平维持在有益的治疗范围内将有助于获得治疗效果,尽管这种可能性应在前瞻性研究中得到证实。

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