Kopylov U, Amre D, Theoret Y, Deslandres C, Seidman E G
*Division of Gastroenterology, McGill University Health Center †Department of Pediatrics, Research Center, Sainte Justine Hospital, University of Montreal, Quebec, Canada.
J Pediatr Gastroenterol Nutr. 2014 Oct;59(4):511-5. doi: 10.1097/MPG.0000000000000455.
Thiopurines (azathioprine, 6-mercaptopurine) are a mainstay of treatment in Crohn disease (CD). Monitoring intracellular metabolite (6-thioguanine nucleotides [6-TGN] and 6-methylmercaptopurine [6-MMP]) levels can help optimize therapeutic efficacy and minimize potential toxicity. Determination of 6-MMP/6-TGN ratios may provide additional useful information, such as the identification of individuals with excessive thiopurine methyltransferase activity and disadvantageous 6-MMP overproduction. These patients are at increased risk of therapeutic failure and hepatotoxicity. The aim of the study was to evaluate the correlation of 6-MMP/6-TGN ratios with therapeutic efficacy and risk of hepatotoxicity in CD.
The present study was a single-center cross-sectional study including pediatric patients with CD studied prospectively with clinical and laboratory assessments along with serial measurements of 6-MMP and 6-TGN. Clinical response was determined using established clinical indices.
The study included 238 pediatric patients with CD with a total of 1648 evaluation points. The patients were in steroid-free remission at 59.1% of the evaluation points. 6-MMP/6-TGN ratios of 4 to 24 were protective against relapse (odds ratio [OR] 0.52, 95% confidence interval [CI] -0.39 to 0.69, P = 0.001). Hepatotoxicity was associated with high 6-MMP levels (>3919 pmol/8 × 10 red blood cell count: OR 7.65, 95% CI 3.7-15.9, P = 0.001) and high 6-MMP/6-TGN ratios (>24: OR 5.35, 95% CI -3.43 to 8.43, P = 0.001).
We observed significant associations between 6-MMP/6-TGN ratios and clinical response, and risk of hepatotoxicity. Our results suggest that determination of thiopurine metabolite ratios is a valuable tool for identification of patients at increased risk of therapeutic failure and hepatotoxicity.
硫唑嘌呤(硫唑嘌呤、6-巯基嘌呤)是克罗恩病(CD)治疗的主要药物。监测细胞内代谢物(6-硫鸟嘌呤核苷酸[6-TGN]和6-甲基巯基嘌呤[6-MMP])水平有助于优化治疗效果并将潜在毒性降至最低。测定6-MMP/6-TGN比值可能会提供额外有用信息,比如识别硫唑嘌呤甲基转移酶活性过高和6-MMP产生不利的个体。这些患者治疗失败和肝毒性风险增加。本研究的目的是评估CD患者中6-MMP/6-TGN比值与治疗效果和肝毒性风险的相关性。
本研究为单中心横断面研究,纳入前瞻性研究的CD儿科患者,进行临床和实验室评估以及6-MMP和6-TGN的系列测量。使用既定临床指标确定临床反应。
该研究纳入238例CD儿科患者,共1648个评估点。在59.1%的评估点患者处于无类固醇缓解状态。6-MMP/6-TGN比值为4至24可预防复发(优势比[OR]0.52,95%置信区间[CI]-0.39至0.69,P=0.001)。肝毒性与高6-MMP水平(>3919 pmol/8×10红细胞计数:OR 7.65,95%CI 3.7-15.9,P=0.001)和高6-MMP/6-TGN比值(>24:OR 5.35,95%CI -3.43至8.43,P=0.001)相关。
我们观察到6-MMP/6-TGN比值与临床反应以及肝毒性风险之间存在显著关联。我们的结果表明,测定硫唑嘌呤代谢物比值是识别治疗失败和肝毒性风险增加患者的有价值工具。