Risk of Infection in Patients With Inflammatory Bowel Disease Treated With Interleukin-Targeting Agents: A Systematic Review and Meta-Analysis.

IF 4.5 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Inflammatory Bowel Diseases Pub Date : 2025-01-06 DOI:10.1093/ibd/izae031
Konstantinos Ouranos, Hira Saleem, Stephanos Vassilopoulos, Athanasios Vassilopoulos, Evangelia K Mylona, Fadi Shehadeh, Markos Kalligeros, Bincy P Abraham, Eleftherios Mylonakis
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Abstract

Background: Patients with inflammatory bowel disease (IBD) are at increased risk of infection. The aim of this study was to assess the cumulative incidence and risk of infection in patients with IBD treated with interleukin (IL)-targeting agents.

Methods: We searched PubMed, EMBASE, and Web of Science for randomized controlled trials including patients with IBD receiving IL-targeting agents compared with patients receiving placebo or treatment that only differed from the intervention arm in the absence of an IL-targeting agent. The primary outcome of interest was the relative risk (RR) of any-grade and severe infection during the induction phase.

Results: There was no difference in risk of any-grade (RR, 0.98; 95% confidence interval [CI], 0.89-1.09) or severe (RR, 0.64; 95% CI, 0.38-1.10) infection in patients receiving any IL-targeting agent compared with the control group. During the maintenance period, the cumulative incidence of any-grade infection in patients receiving IL-12/23p40-targeting agents (mean follow-up 29 weeks) was 34.82% (95% CI, 26.78%-43.32%), while the cumulative incidence of severe infection was 3.07% (95% CI, 0.93%-6.21%). The cumulative incidence of any-grade infection in patients receiving IL-23p19-targeting agents (mean follow-up 40.9 weeks) was 32.16% (95% CI, 20.63%-44.88%), while the cumulative incidence of severe infection was 1.75% (95% CI, 0.60%-3.36%). During the maintenance phase of the included studies, the incidence of infection was 30.66% (95% CI, 22.12%-39.90%) for any-grade and 1.59% (95% CI, 0.76%-2.63%) for severe infection in patients in the control group.

Conclusions: There was no difference in risk of infection between patients with IBD who received IL-targeting agents compared with the control group. Case registries and randomized controlled trials reporting the safety of IL inhibitors should provide detailed information about the risk of specific infectious complications in patients with IBD receiving IL-targeting agents.

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使用白细胞介素靶向药物治疗的炎症性肠病患者的感染风险:系统回顾与元分析》。
背景:炎症性肠病(IBD)患者感染风险增加。本研究旨在评估接受白细胞介素(IL)靶向药物治疗的 IBD 患者的累积感染率和感染风险:我们在PubMed、EMBASE和Web of Science上搜索了随机对照试验,这些试验包括接受IL靶向药物治疗的IBD患者与接受安慰剂治疗的患者,或仅在未使用IL靶向药物的情况下与干预组不同的治疗。主要研究结果是诱导阶段发生任何等级和严重感染的相对风险(RR):结果:与对照组相比,接受任何一种IL靶向药物治疗的患者发生任何等级感染(RR,0.98;95% 置信区间[CI],0.89-1.09)或严重感染(RR,0.64;95% CI,0.38-1.10)的风险没有差异。在维持治疗期间,接受IL-12/23p40靶向药物治疗的患者(平均随访29周)的任何级别感染的累积发生率为34.82%(95% CI,26.78%-43.32%),而严重感染的累积发生率为3.07%(95% CI,0.93%-6.21%)。在接受IL-23p19靶向药物治疗的患者中(平均随访40.9周),任何级别感染的累积发生率为32.16%(95% CI,20.63%-44.88%),而严重感染的累积发生率为1.75%(95% CI,0.60%-3.36%)。在纳入研究的维持阶段,对照组患者的任何等级感染发生率为30.66%(95% CI,22.12%-39.90%),严重感染发生率为1.59%(95% CI,0.76%-2.63%):结论:与对照组相比,接受IL靶向药物治疗的IBD患者感染风险没有差异。报告IL抑制剂安全性的病例登记和随机对照试验应提供有关接受IL靶向药物治疗的IBD患者发生特定感染并发症风险的详细信息。
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来源期刊
Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 医学-胃肠肝病学
CiteScore
9.70
自引率
6.10%
发文量
462
审稿时长
1 months
期刊介绍: Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.
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