Antibiotic Exposure and Risk of New-Onset Inflammatory Bowel Disease: A Systematic Review and Dose-Response Meta-Analysis.

IF 11.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Clinical Gastroenterology and Hepatology Pub Date : 2025-01-01 Epub Date: 2024-02-28 DOI:10.1016/j.cgh.2024.02.010
Ruqiao Duan, Cunzheng Zhang, Gaonan Li, Jun Li, Liping Duan
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Abstract

Background & aims: The association between antibiotic exposure and inflammatory bowel disease (IBD) remains controversial, especially whether there is a dose-response relationship. We aimed to conduct a systematic review and meta-analysis to thoroughly evaluate the risk of new-onset IBD associated with antibiotic exposure.

Methods: Four databases were searched from their inception to September 30, 2023 for all relevant studies. The risk estimates were pooled together using random-effects models, and pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated, stratified by IBD subtype, age, exposure period, study type, and antibiotic classes. Dose-response relationship between the number of antibiotic prescriptions and IBD risk was assessed using generalized least squares regression analysis.

Results: Twenty-eight studies involving 153,027 patients with IBD were included. Antibiotic exposure was significantly associated with an increased risk of new-onset IBD for prescription-based studies (pooled OR, 1.41; 95% CI, 1.29-1.53) and for questionnaire-based studies (pooled OR, 1.35; 95% CI, 1.08-1.68). This association existed for both Crohn's disease and ulcerative colitis, as well as in children and adults for prescription-based studies. The majority of antibiotic classes were associated with an increased IBD risk, with metronidazole (OR, 1.70; 95% CI, 1.38-2.10) and quinolones (OR, 1.56; 95% CI, 1.37-1.77) having relatively higher risk estimates. A positive nonlinear dose-response association was observed between the number of antibiotic prescriptions and IBD risk.

Conclusions: Antibiotic exposure was significantly associated with an increased risk of new-onset IBD, and a positive nonlinear dose-response relationship was observed. Antibiotic stewardship may be important for reducing IBD risk.

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抗生素暴露与新发炎症性肠病的风险:系统回顾与剂量反应荟萃分析。
背景和目的:抗生素暴露与炎症性肠病(IBD)之间的关系仍存在争议,尤其是是否存在剂量反应关系。我们旨在进行一项系统回顾和荟萃分析,以全面评估与抗生素暴露相关的新发 IBD 风险:方法:我们在四个数据库中检索了从开始到 2023 年 9 月 30 日的所有相关研究。采用随机效应模型对风险估计值进行了汇总,并按IBD亚型、年龄、暴露期、研究类型和抗生素类别计算了汇总的几率比(OR)和95%置信区间(CI)。使用广义最小二乘法回归分析评估了抗生素处方数量与 IBD 风险之间的剂量-反应关系:结果:共纳入28项研究,涉及153027名IBD患者。在基于处方的研究(汇总 OR = 1.41,95% CI 1.29-1.53)和基于问卷的研究(汇总 OR = 1.35,95% CI 1.08-1.68)中,抗生素暴露与新发 IBD 风险的增加明显相关。在基于处方的研究中,克罗恩病和溃疡性结肠炎以及儿童和成人都存在这种关联。大多数抗生素类别都与 IBD 风险增加有关,其中甲硝唑(OR = 1.70,95% CI 1.38-2.10)和喹诺酮类(OR = 1.56,95% CI 1.37-1.77)的风险估计值相对较高。抗生素处方数量与 IBD 风险之间存在正向非线性剂量反应关系:结论:抗生素暴露与新发 IBD 风险的增加密切相关,并观察到正向非线性剂量-反应关系。抗生素管理对于降低 IBD 风险可能很重要。
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来源期刊
CiteScore
16.90
自引率
4.80%
发文量
903
审稿时长
22 days
期刊介绍: Clinical Gastroenterology and Hepatology (CGH) is dedicated to offering readers a comprehensive exploration of themes in clinical gastroenterology and hepatology. Encompassing diagnostic, endoscopic, interventional, and therapeutic advances, the journal covers areas such as cancer, inflammatory diseases, functional gastrointestinal disorders, nutrition, absorption, and secretion. As a peer-reviewed publication, CGH features original articles and scholarly reviews, ensuring immediate relevance to the practice of gastroenterology and hepatology. Beyond peer-reviewed content, the journal includes invited key reviews and articles on endoscopy/practice-based technology, health-care policy, and practice management. Multimedia elements, including images, video abstracts, and podcasts, enhance the reader's experience. CGH remains actively engaged with its audience through updates and commentary shared via platforms such as Facebook and Twitter.
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