接受非抗-TNF 生物制剂或抗-TNF-α 制剂治疗的韩国炎症性肠病患者发生严重感染和结核病的比较风险:一项基于全国人口的队列研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-07-31 eCollection Date: 2024-01-01 DOI:10.1177/17562848241265013
Min Jee Kim, Ye-Jee Kim, Daehyun Jeong, Seonok Kim, Seokchan Hong, Sang Hyoung Park, Kyung-Wook Jo
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引用次数: 0

摘要

背景:在韩国人群中,尚未根据抗肿瘤坏死因子(TNF)-α药物与非抗肿瘤坏死因子生物制剂(维妥珠单抗/奥司替尼)的使用情况同时评估炎症性肠病(IBD)患者发生严重感染和活动性肺结核的风险:我们比较了接受非抗-TNF生物制剂(维妥珠单抗/奥司替尼)或抗-TNF-α制剂治疗的韩国IBD患者发生严重感染和活动性肺结核的风险:方法:回顾2007年1月至2021年2月期间健康保险审查和评估服务的索赔数据(占韩国人口的97%),纳入2017年至2020年期间开始使用维多珠单抗/奥斯特库单抗或抗-TNF-α治疗的成人IBD患者(n = 6123)。分析了随访期间需要住院/急诊就诊的严重感染或活动性肺结核风险的组间差异:在平均随访1.55±1.05年和0.84±0.69年期间接受抗TNF-α药物或维多珠单抗/奥司替尼治疗的患者中,严重感染发生率分别为9.43/100人年和6.87/100人年。多变量分析显示,使用维多珠单抗/奥司替尼或抗肿瘤坏死因子-α治疗的严重感染风险在组间无明显差异;与抗肿瘤坏死因子-α药物相比,使用维多珠单抗/奥司替尼的调整后相对风险为0.81(95%置信区间为0.46-1.44,P = 0.478)。在接受抗肿瘤坏死因子-α药物和维多珠单抗/奥司替尼治疗的患者中,活动性肺结核的发病率分别为每100人年0.87例和0.37例。与抗肿瘤坏死因子-α药物相比,维多珠单抗/奥司替尼的相对风险为0.31(95%置信区间为0.07-1.26,P = 0.101)。在比较维多珠单抗和乌斯特库单抗与抗肿瘤坏死因子-α药物的子集分析中,也观察到类似的结果:结论:在韩国IBD患者中,与抗肿瘤坏死因子α药物相比,非抗肿瘤坏死因子生物制剂(维多利珠单抗/乌斯特库单抗)发生严重感染或活动性肺结核的风险较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative risk of serious infections and tuberculosis in Korean patients with inflammatory bowel disease treated with non-anti-TNF biologics or anti-TNF-α agents: a nationwide population-based cohort study.

Background: The risk of serious infection and active tuberculosis in patients with inflammatory bowel disease (IBD) has not been concurrently evaluated based on the use of anti-tumor necrosis factor (TNF)-α agents versus non-anti-TNF biologics (vedolizumab/ustekinumab) in the Korean population.

Objectives: We compared the risk of serious infection and active tuberculosis in Korean patients with IBD treated with non-anti-TNF biologics (vedolizumab/ustekinumab) or anti-TNF-α agents.

Design: This study was a population-based cohort analysis of nationwide administrative claims data.

Methods: Health Insurance Review and Assessment Service claims data (representing 97% of the South Korean population) from between January 2007 and February 2021 were reviewed, and adults with IBD who initiated vedolizumab/ustekinumab or anti-TNF-α treatment (n = 6123) between 2017 and 2020 were enrolled. Intergroup differences in the risk of serious infection requiring hospitalization/emergency department visits or active tuberculosis during the follow-up period were analyzed.

Results: In the patients treated with anti-TNF-α agents or vedolizumab/ustekinumab during a mean follow-up of 1.55 ± 1.05 and 0.84 ± 0.69 years, the incidence rates of serious infection were 9.43/100 and 6.87/100 person-years, respectively. Multivariable analysis showed no significant intergroup difference in the risk of serious infection with vedolizumab/ustekinumab or anti-TNF-α treatment; the adjusted relative risk of vedolizumab/ustekinumab compared with anti-TNF-α agents was 0.81 (95% confidence interval 0.46-1.44, p = 0.478). Among patients treated with anti-TNF-α agents and vedolizumab/ustekinumab, the incidence rates of active tuberculosis were 0.87 and 0.37 per 100 person-years, respectively. The relative risk of vedolizumab/ustekinumab compared with anti-TNF-α agents was 0.31 (95% confidence interval 0.07-1.26, p = 0.101). In a subset analysis comparing vedolizumab and ustekinumab with anti-TNF-α agents, similar results were observed.

Conclusion: In Korean patients with IBD, non-anti-TNF biologics (vedolizumab/ustekinumab) tended to be associated with a lower risk of serious infection or active tuberculosis than anti-TNF-α agents.

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