Pharmacie Clinique, Pharmacocinétique et Évaluation du Médicament, Université de Lyon, Université Lyon 1, Lyon, France.
Ther Drug Monit. 2013 Apr;35(2):251-7. doi: 10.1097/FTD.0b013e318282c3a6.
Previous studies have reported no or only a very poor correlation between 6-methylmercaptopurine/6-thioguanine nucleotide (6-MeMPN/6-TGN) and azathioprine (AZA) dose in the treatment of inflammatory bowel disease (IBD). However, metabolite levels are often repeatedly measured yielding a hierarchical data structure that requires more appropriate data analysis.
This study explored the relationship between the weight-based dosage of AZA and metabolites levels in 86 pediatric IBD patients using multilevel analysis. Other covariates related to patient characteristics and treatment were evaluated.
This is the first study to demonstrate positive correlations between AZA dose and 6-TGN and 6-MeMPN levels and 6-MeMPN/6-TGN ratio (P < 0.001) in IBD children. Other novel predictors of metabolites were reported. Younger children exhibited lower 6-TGN and 6-MeMPN levels, probably suggesting age-related differences in metabolism and/or absorption of thiopurines. Coadministration of infliximab resulted in a significant increase in 6-TGN levels (P = 0.023). Moreover, alanine aminotransferase values positively correlated with 6-MeMPN levels (P = 0.032). The duration of AZA therapy, gender, and thiopurine methyltransferase activity were associated with metabolite levels. The wide interindividual variability in metabolite levels that accounted for 67.7%, 48.6%, and 49.4% of variance in the 6-TGN and 6-MeMPN levels and the ratio, respectively, were confirmed.
The reliable AZA dose-metabolites relationship is useful for clinicians to guide the dosing regimen to maximize clinical response and minimize side effects or to consider alternative therapies when patients have preferential production of the toxic 6-MeMPN. These results may be of potential interest for optimizing thiopurine therapy to achieve safe and efficacious AZA use in pediatric IBD patients.
既往研究报道,在炎症性肠病(IBD)的治疗中,6-甲基巯基嘌呤/6-硫代鸟嘌呤核苷酸(6-MeMPN/6-TGN)与硫唑嘌呤(AZA)剂量之间无相关性或仅有很差的相关性。然而,代谢物水平通常是反复测量的,这导致了数据呈现出层次结构,需要更合适的数据分析方法。
本研究使用多水平分析方法,探讨了 86 例儿科 IBD 患者中基于体重的 AZA 剂量与代谢物水平之间的关系。评估了与患者特征和治疗相关的其他协变量。
这是第一项表明在 IBD 儿童中,AZA 剂量与 6-TGN 和 6-MeMPN 水平以及 6-MeMPN/6-TGN 比值之间呈正相关(P<0.001)的研究。还报告了其他新型代谢物预测因子。年龄较小的患儿表现出较低的 6-TGN 和 6-MeMPN 水平,可能提示代谢和/或硫嘌呤吸收存在与年龄相关的差异。英夫利昔单抗的联合用药导致 6-TGN 水平显著升高(P=0.023)。此外,丙氨酸氨基转移酶值与 6-MeMPN 水平呈正相关(P=0.032)。AZA 治疗持续时间、性别和硫嘌呤甲基转移酶活性与代谢物水平相关。代谢物水平的个体间变异性较大,分别解释了 6-TGN 和 6-MeMPN 水平以及比值的 67.7%、48.6%和 49.4%的变异性。
可靠的 AZA 剂量-代谢物关系有助于临床医生指导剂量调整方案,以最大限度地提高临床疗效,最小化不良反应,或在患者优先产生毒性 6-MeMPN 时考虑替代治疗。这些结果可能对优化硫嘌呤治疗以实现儿科 IBD 患者安全有效的 AZA 使用具有潜在意义。