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在炎症性肠病患者中,别嘌醇和硫唑嘌呤或 6-巯基嘌呤的长期疗效和安全性。

Long term efficacy and safety of allopurinol and azathioprine or 6-mercaptopurine in patients with inflammatory bowel disease.

机构信息

Section of Gastroenterology, Hepatology and Nutrition, University of Chicago Medical Center, 5841 S Maryland Ave MC 4076, Chicago, Illinois, USA.

出版信息

J Crohns Colitis. 2009 Sep;3(3):162-7. doi: 10.1016/j.crohns.2009.02.003. Epub 2009 Mar 17.

DOI:10.1016/j.crohns.2009.02.003
PMID:21172265
Abstract

BACKGROUND AND AIMS

We previously reported that IBD patients who are non-responders to thiopurines with preferential shunting of metabolites to hepatotoxic 6-methylmercaptopurine ribonucleotides compared to 6-thioguanine nucleotides can reverse the ratio of 6-MMP/6-TGN and respond to thiopurines with the addition of allopurinol. The objective of this study is to report long term efficacy and safety, along with results for an additional 11 patients.

METHODS

Retrospective chart review of patients at the University of Chicago IBD Center treated with allopurinol in addition to thiopurines.

RESULTS

Twenty five patients with Crohn's disease or ulcerative colitis were enrolled. Within the first month of therapy 6-TGN metabolite levels increased from a mean of 186.5±17.4 (SE) to 352.8±37.8 pmol/8×10(8) (p=0.0001). Over the same period 6-MMP levels decreased from a mean of 11,966±1697 to 2004±536 pmol/8×10(8) (p<0.0001). The mean daily dosage of prednisone decreased from 19.8±3.8 mg to 5.3±2.7 mg (p=0.03). Thirteen patients have a minimum of one year follow-up. Nine of these thirteen patients have continued on therapy for at least 2 years. All thirteen of these patients continue to be in clinical remission at the last follow-up visit. No patients have had evidence of sustained thrombocytopenia or abnormal liver enzymes.

CONCLUSIONS

In AZA/6-MP non-responders with increased 6-MMP/6-TGN ratios, addition of allopurinol continues to demonstrate safety and efficacy for long-term maintenance and steroid-sparing in IBD.

摘要

背景和目的

我们之前报道过,与 6-硫代鸟嘌呤核苷酸相比,对硫嘌呤无反应的 IBD 患者,其代谢产物优先分流到肝毒性 6-甲基巯基嘌呤核苷酸,可逆转 6-MMP/6-TGN 比值,并通过添加别嘌呤醇对硫嘌呤产生反应。本研究的目的是报告长期疗效和安全性,并报告另外 11 例患者的结果。

方法

对芝加哥大学 IBD 中心接受硫嘌呤联合别嘌呤醇治疗的患者进行回顾性图表审查。

结果

25 例克罗恩病或溃疡性结肠炎患者入组。在治疗的第一个月,6-TGN 代谢物水平从平均 186.5±17.4(SE)增加到 352.8±37.8 pmol/8×10(8)(p=0.0001)。在此期间,6-MMP 水平从平均 11,966±1697 降低到 2004±536 pmol/8×10(8)(p<0.0001)。泼尼松的平均日剂量从 19.8±3.8 mg 降低到 5.3±2.7 mg(p=0.03)。13 例患者的随访时间至少为 1 年。其中 9 例患者至少连续 2 年接受治疗。所有 13 例患者在最后一次随访时仍处于临床缓解状态。无患者出现持续血小板减少或肝功能异常。

结论

在 AZA/6-MP 无反应者中,增加 6-MMP/6-TGN 比值,添加别嘌呤醇继续为 IBD 的长期维持和类固醇节约提供安全性和疗效。

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