克罗恩病患者在使用硫嘌呤和甲氨蝶呤时临床失败风险的差异:一项基于韩国全国人口的研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-05-12 eCollection Date: 2024-01-01 DOI:10.1177/17562848241248321
Yu Kyung Jun, Eunjeong Ji, Hye Ran Yang, Yonghoon Choi, Cheol Min Shin, Young Soo Park, Nayoung Kim, Dong Ho Lee, Hyuk Yoon
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引用次数: 0

摘要

背景:尽管克罗恩病(CD)患者广泛使用免疫调节剂,但目前尚不清楚硫嘌呤类药物和甲氨蝶呤(MTX)的治疗效果是否存在差异:目的:比较硫嘌呤类药物和MTX对生物无效的克罗恩病患者临床治疗失败的风险:设计:全国性、基于人群的研究:我们使用了韩国国民健康保险服务的理赔数据。在对治疗进行反概率加权后,采用逻辑回归和 Cox 比例危险分析来评估接受硫嘌呤(硫嘌呤组)或 MTX(MTX 组)治疗的 CD 患者临床治疗失败的风险:共纳入10296名成人和儿童CD患者[硫嘌呤组和MTX组分别为9912人(96.3%)和384人(3.7%)]。MTX组未能诱导缓解的几率(ORs)明显高于硫嘌呤组[调整后OR(aOR),1.115;95%置信区间(CI),1.045-1.190;P = 0.001]。然而,仅在未同时使用类固醇的患者中观察到相反的结果:MTX 组诱导失败的风险低于硫嘌呤组(aOR,0.740;95% 置信区间(CI),0.673-0.813;P = 0.001]。标准剂量 MTX 组发生总体维持治疗失败的风险高于低剂量 MTX 组(aHR:1.296;95% CI:1.134-1.480;P 结论:硫嘌呤比呋喃妥因更有效:硫嘌呤比MTX更能有效诱导和维持生化免疫缺陷CD患者的病情缓解;然而,同时使用类固醇会影响病情缓解的诱导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differences in the risk of clinical failure between thiopurine and methotrexate in bio-naïve patients with Crohn's disease: a Korean nationwide population-based study.

Background: Although immunomodulators are widely prescribed in patients with Crohn's disease (CD), it is unclear whether there is a difference in treatment outcomes between thiopurines and methotrexate (MTX).

Objective: To compare the risk of clinical failure between thiopurines and MTX in bio-naïve patients with CD.

Design: Nationwide, population-based study.

Methods: We used claims data from the Korean National Health Insurance Service. After inverse probability of treatment weighting, logistic regression and Cox proportional hazard analyses were used to evaluate the risk of clinical failure in bio-naïve patients with CD treated with thiopurine (thiopurine group) or MTX (MTX group).

Results: Overall, 10,296 adult and pediatric patients with CD [9912 (96.3%) and 384 (3.7%) in the thiopurine and MTX groups, respectively] were included. The odds ratios (ORs) of failure to induce remission were significantly higher in the MTX group than in the thiopurine group [adjusted OR (aOR), 1.115; 95% confidence interval (CI), 1.045-1.190; p = 0.001]. However, the opposite result was observed only in patients without concomitant steroid use: the MTX group had a lower risk of induction failure than the thiopurine group (aOR, 0.740; 95% CI, 0.673-0.813; p < 0.001). The risk of overall maintenance failure was higher in the MTX group than in the thiopurine group [adjusted hazard ratio (aHR), 1.117; 95% CI, 1.047-1.191; p = 0.001]. The risk of overall maintenance failure was higher in the standard-dose MTX group than in the low-dose MTX group (aHR, 1.296; 95% CI, 1.134-1.480; p < 0.001). There was no significant difference in the risk of maintenance failure according to the administration route of MTX.

Conclusion: Thiopurine is more effective than MTX in inducing and maintaining remission in bio-naïve patients with CD; however, the concomitant use of steroids influences inducing remission.

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