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对于正在接受6-巯基嘌呤或硫唑嘌呤治疗且病情缓解的炎症性肠病成人和儿童,5-氨基水杨酸疗法与较高的6-硫鸟嘌呤水平相关。

5-aminosalicylate therapy is associated with higher 6-thioguanine levels in adults and children with inflammatory bowel disease in remission on 6-mercaptopurine or azathioprine.

作者信息

Hande Scott, Wilson-Rich Noah, Bousvaros Athos, Zholudev Anna, Maurer Rie, Banks Peter, Makrauer Frederick, Reddy Sarathchandra, Burakoff Robert, Friedman Sonia

机构信息

Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

Inflamm Bowel Dis. 2006 Apr;12(4):251-7. doi: 10.1097/01.MIB.0000206544.05661.9f.


DOI:10.1097/01.MIB.0000206544.05661.9f
PMID:16633046
Abstract

BACKGROUND: Small uncontrolled trials have suggested that 5-aminosalicylate (5-ASA) medications increase 6-thioguanine nucleotide (6-TGn) levels in adults with Crohn's disease (CD) on azathioprine (AZA) or 6-mercaptopurine (6-MP), presumably through the inhibition of thiopurine methyltransferase (TPMT). We tested the theory that coadministration of 5-ASA agents with AZA/6-MP results in higher 6-TGn levels in a large cohort of children and adults with CD or ulcerative colitis (UC). METHODS: A retrospective cohort study identified all children and adults treated for IBD with AZA/6-MP at 2 tertiary medical centers. Patients were included if their TPMT genotype was known and 6-TGn and 6-methymercaptopurine (6-MMP) levels had been obtained after 3 months of clinical remission at a stable dose of AZA/6-MP. 6-TGn and 6-MMP levels were compared between patients taking and those not taking 5-ASA medications through the use of linear regression models to identify and adjust for potentially confounding variables. RESULTS: Of the 126 patients included, 88 were taking 5-ASA medications. Patients on 5-ASA agents had higher mean 6-TGn levels after adjustment for confounding variables (Delta6-TGn, 47.6 +/- 21.8 pmol/8 x 10 red blood cells; P = 0.03). CD and TPMT heterozygosity was independently associated with higher 6-TGn levels (P = 0.01 and P = 0.03, respectively). 5-ASA exposure was not associated with a change in 6-MMP levels. CONCLUSIONS: We found that 5-ASA therapy is associated with higher 6-TGn levels in children and adults with IBD on 6-MP/AZA. TPMT inhibition may not explain this effect because 5-ASA exposure did not affect 6-MMP levels. The observed association of CD with higher 6-TGn levels is novel and needs to be verified in prospective studies.

摘要

背景:小型非对照试验表明,5-氨基水杨酸(5-ASA)类药物可使接受硫唑嘌呤(AZA)或6-巯基嘌呤(6-MP)治疗的克罗恩病(CD)成年患者的6-硫鸟嘌呤核苷酸(6-TGn)水平升高,推测其机制是抑制硫嘌呤甲基转移酶(TPMT)。我们验证了以下理论:在一大群患有CD或溃疡性结肠炎(UC)的儿童和成人中,5-ASA制剂与AZA/6-MP联合使用会使6-TGn水平升高。 方法:一项回顾性队列研究纳入了在两家三级医疗中心接受AZA/6-MP治疗的所有IBD儿童和成人。如果患者的TPMT基因型已知,且在以稳定剂量的AZA/6-MP达到临床缓解3个月后获得了6-TGn和6-甲基巯基嘌呤(6-MMP)水平,则纳入研究。通过线性回归模型比较服用和未服用5-ASA药物的患者的6-TGn和6-MMP水平,以识别和调整潜在的混杂变量。 结果:纳入的126例患者中,88例正在服用5-ASA药物。在对混杂变量进行调整后,服用5-ASA制剂的患者的平均6-TGn水平更高(Δ6-TGn,47.6±21.8 pmol/8×10⁶红细胞;P=0.03)。CD和TPMT杂合性分别与较高的6-TGn水平独立相关(P=0.01和P=0.03)。5-ASA暴露与6-MMP水平的变化无关。 结论:我们发现,在接受6-MP/AZA治疗的IBD儿童和成人中,5-ASA治疗与较高的6-TGn水平相关。TPMT抑制可能无法解释这种效应,因为5-ASA暴露并未影响6-MMP水平。观察到的CD与较高6-TGn水平之间的关联是新发现,需要在前瞻性研究中进行验证。

相似文献

[1]
5-aminosalicylate therapy is associated with higher 6-thioguanine levels in adults and children with inflammatory bowel disease in remission on 6-mercaptopurine or azathioprine.

Inflamm Bowel Dis. 2006-4

[2]
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[3]
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[4]
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Inflamm Bowel Dis. 2007-4

[5]
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Clin Gastroenterol Hepatol. 2004-5

[6]
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World J Gastroenterol. 2015-3-28

[7]
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J Gastroenterol Hepatol. 2008-9

[8]
Does lymphopenia or macrocytosis reflect 6-thioguanine levels in patients with inflammatory bowel disease treated with azathioprine or 6-mercaptopurine?

Intern Med J. 2016-4

[9]
A 6-thioguanine nucleotide threshold level of 400 pmol/8 x 10(8) erythrocytes predicts azathioprine refractoriness in patients with inflammatory bowel disease and normal TPMT activity.

Am J Gastroenterol. 2008-12

[10]
Thiopurine maintenance therapy for ulcerative colitis: the clinical significance of monitoring 6-thioguanine nucleotide.

Inflamm Bowel Dis. 2010-8

引用本文的文献

[1]
Proactive pharmacogenomics in azathioprine-treated pediatric inflammatory bowel disease at a Chinese tertiary hospital.

Front Pharmacol. 2025-3-26

[2]
Real-world NUDT15 genotyping and thiopurine treatment optimization in inflammatory bowel disease: a multicenter study.

J Gastroenterol. 2024-6

[3]
Concomitant 5-aminosalicylic acid treatment does not affect 6-thioguanine nucleotide levels in patients with inflammatory bowel disease on thiopurines.

Ann Gastroenterol. 2023

[4]
The Role of Pharmacogenetics in the Therapeutic Response to Thiopurines in the Treatment of Inflammatory Bowel Disease: A Systematic Review.

J Clin Med. 2023-10-25

[5]
Risk-stratified monitoring for thiopurine toxicity in immune-mediated inflammatory diseases: prognostic model development, validation, and, health economic evaluation.

EClinicalMedicine. 2023-9-14

[6]
No Benefit of Continuing 5-Aminosalicylates in Patients with Crohn's Disease Treated with Anti-metabolite Therapy.

Dig Dis Sci. 2022-7

[7]
Advances in Thiopurine Drug Delivery: The Current State-of-the-Art.

Eur J Drug Metab Pharmacokinet. 2021-11

[8]
Xanthine oxidase activity in thiopurine curative Chinese inflammatory bowel disease patients.

Pharmacol Res Perspect. 2021-5

[9]
Thiopurines' Metabolites and Drug Toxicity: A Meta-Analysis.

J Clin Med. 2020-7-13

[10]
No benefit of continuing vs stopping 5-aminosalicylates in patients with ulcerative colitis escalated to anti-metabolite therapy.

Aliment Pharmacol Ther. 2020-6-23

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