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硫唑嘌呤过敏后6-巯基嘌呤治疗炎症性肠病的疗效

Efficacy of 6-mercaptopurine treatment after azathioprine hypersensitivity in inflammatory bowel disease.

作者信息

Nagy Ferenc, Molnar Tamas, Szepes Zoltan, Farkas Klaudia, Nyari Tibor, Lonovics Janos

机构信息

First Department of Medicine, Faculty of Medicine, University of Szeged, Szeged, Hungary.

出版信息

World J Gastroenterol. 2008 Jul 21;14(27):4342-6. doi: 10.3748/wjg.14.4342.

Abstract

AIM

To investigate the efficacy of 6-mercaptopurine (6-MP) in cases of azathioprine (AZA) hypersensitivity in patients with inflammatory bowel disease.

METHODS

Twenty nine previously confirmed Crohn's disease (CD) (n = 14) and ulcerative colitis (UC) (n = 15) patients with a known previous (AZA) hypersensitivity reaction were studied prospectively. The 6-MP doses were gradually increased from 0.5 up to 1.0-1.5 mg/kg per day. Clinical activity indicies (CDAI/CAI), laboratory variables and daily doses of oral 5-ASA, corticosteroids, and 6-MP were assessed before and in the first, sixth and twelfth months of treatment.

RESULTS

In 9 patients, 6-MP was withdrawn in the first 2 wk due to an early hypersensitivity reaction. Medication was ineffective within 6 mo in 6 CD patients, and myelotoxic reaction was observed in two. Data were evaluated at the end of the sixth month in 12 (8 UC, 4 CD) patients, and after the first year in 9 (6 UC, 3 CD) patients. CDAI decreased transiently at the end of the sixth month, but no significant changes were observed in the CDAI or the CAI values at the end of the year. Leukocyte counts (P = 0.01), CRP (P = 0.02), and serum iron (P = 0.05) values indicated decreased inflammatory reactions, especially in the UC patients at the end of the year, making the possibility to taper oral steroid doses.

CONCLUSION

About one-third of the previously AZA-intolerant patients showed adverse effects on taking 6MP. In our series, 20 patients tolerated 6MP, but it was ineffective in 8 CD cases, and valuable mainly in ulcerative colitis patients.

摘要

目的

研究6-巯基嘌呤(6-MP)对炎症性肠病患者硫唑嘌呤(AZA)过敏的疗效。

方法

前瞻性研究29例先前确诊的克罗恩病(CD)(n = 14)和溃疡性结肠炎(UC)(n = 15)患者,这些患者既往有已知的(AZA)过敏反应。6-MP剂量从每天0.5mg/kg逐渐增加至1.0 - 1.5mg/kg。在治疗前以及治疗的第1、6和12个月评估临床活动指标(CDAI/CAI)、实验室指标以及口服5-ASA、皮质类固醇和6-MP的每日剂量。

结果

9例患者在最初2周内由于早期过敏反应停用6-MP。6例CD患者在6个月内药物治疗无效,2例出现骨髓毒性反应。对12例(8例UC,4例CD)患者在第6个月末进行数据评估,对9例(6例UC,3例CD)患者在第1年末进行评估。第6个月末CDAI短暂下降,但在年末CDAI或CAI值未见显著变化。白细胞计数(P = 0.01)、CRP(P = 0.02)和血清铁(P = 0.05)值表明炎症反应减轻,尤其是在年末的UC患者中,使得有可能逐渐减少口服类固醇剂量。

结论

约三分之一先前不耐受AZA的患者服用6MP时出现不良反应。在我们的研究系列中,20例患者耐受6MP,但在8例CD病例中无效,主要对溃疡性结肠炎患者有价值。

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本文引用的文献

1
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Aliment Pharmacol Ther. 2008 Feb 1;27(3):220-7. doi: 10.1111/j.1365-2036.2007.03570.x. Epub 2007 Nov 6.
2
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J Clin Gastroenterol. 2007 Aug;41(7):682-8. doi: 10.1097/01.mcg.0000225577.81008.ee.
3
Therapeutic drug monitoring in patients with inflammatory bowel disease and established azathioprine therapy.
Clin Drug Investig. 2004;24(8):479-86. doi: 10.2165/00044011-200424080-00006.
5
Drug insight: aminosalicylates for the treatment of IBD.
Nat Clin Pract Gastroenterol Hepatol. 2007 Mar;4(3):160-70. doi: 10.1038/ncpgasthep0696.
6
Advances in the medical therapy of inflammatory bowel disease.
Curr Opin Gastroenterol. 2002 Jul;18(4):435-40. doi: 10.1097/00001574-200207000-00007.
7
Pharmacogenetics in inflammatory bowel disease.
World J Gastroenterol. 2006 Jun 21;12(23):3657-67. doi: 10.3748/wjg.v12.i23.3657.
9
Pharmacogenomics in inflammatory bowel disease.
Clin Gastroenterol Hepatol. 2006 Jan;4(1):21-8. doi: 10.1016/j.cgh.2005.10.003.
10
The thiopurines: an update.
Invest New Drugs. 2005 Dec;23(6):523-32. doi: 10.1007/s10637-005-4020-8.

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