A Systematic Review and Meta-Analysis: Adverse Inflammatory Bowel Disease Outcomes Following Acute COVID-19

Gastro hep advances Pub Date : 2025-01-01 Epub Date: 2024-10-24 DOI:10.1016/j.gastha.2024.10.021
Evangelin Shaloom Vitus , Simran Mann , Charlie W. Lees , Tine Jess , Rahma Elmahdi
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Abstract

Background and Aims

Respiratory viral infections have been implicated in the exacerbation of immune-mediated inflammatory diseases such as inflammatory bowel disease (IBD). To understand the impact of early SARS-CoV-2 variants on the risk of adverse IBD outcomes, we aimed to perform a meta-analysis of high-quality studies.

Methods

Cohort studies investigating adverse IBD outcomes (IBD flares, change in disease activity, change in medication, IBD-related hospitalization, and surgery) following COVID-19 were retrieved from MEDLINE and Embase. The Risk Of Bias In Nonrandomized Studies—of Exposure tool was used to assess risk of bias. Random effects model meta-analysis was used to calculate the hazard ratio (HR) for risk of adverse outcomes. Subgroup analysis was performed to estimate risk of outcomes for ulcerative colitis and Crohn’s disease patients. Metaregression was performed for sex and duration of follow-up.

Results

Of the 3119 identified studies, 5 were included in the meta-analysis. A total of 34,977 IBD patients with COVID-19 and 53,270 IBD patients without recorded COVID-19 infection were identified. Two of the studies showed a high risk of bias. The random effects model did not show a statistically significant increase in the risk of adverse IBD outcomes following COVID infection (HR:1.05 [0.75–1.46]). There was no significant difference in adverse outcomes between Crohn’s disease (HR: 0.91 [0.82–1.02]) and ulcerative colitis patients (HR: 0.83 [0.76–0.90]). Neither the proportion of male participants nor the mean duration of follow-up were found to be significant predictors of effect size.

Conclusion

In this systematic review and meta-analysis, we find that COVID-19 did not increase the risk of adverse IBD outcomes.
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一项系统综述和荟萃分析:急性COVID-19后炎症性肠病的不良结局
背景和目的呼吸道病毒感染与免疫介导的炎症性疾病(如炎症性肠病(IBD))的恶化有关。为了了解早期SARS-CoV-2变异对IBD不良结局风险的影响,我们旨在对高质量研究进行荟萃分析。方法从MEDLINE和Embase检索调查COVID-19后IBD不良结局(IBD发作、疾病活动度变化、药物变化、IBD相关住院和手术)的简短研究。使用非随机研究的偏倚风险-暴露工具来评估偏倚风险。采用随机效应模型meta分析计算不良结局风险的风险比(HR)。进行亚组分析以估计溃疡性结肠炎和克罗恩病患者结局的风险。对性别和随访时间进行回归分析。在3119项确定的研究中,有5项纳入了meta分析。共发现34977例合并COVID-19的IBD患者和53270例未记录COVID-19感染的IBD患者。其中两项研究显示出较高的偏倚风险。随机效应模型未显示COVID感染后IBD不良结局的风险有统计学意义的增加(HR:1.05[0.75-1.46])。克罗恩病(HR: 0.91[0.82-1.02])和溃疡性结肠炎(HR: 0.83[0.76-0.90])患者的不良结局无显著差异。男性参与者的比例和平均随访时间均未被发现是效应大小的显著预测因子。结论在本系统综述和荟萃分析中,我们发现COVID-19并未增加IBD不良结局的风险。
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来源期刊
Gastro hep advances
Gastro hep advances Gastroenterology
CiteScore
0.80
自引率
0.00%
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0
审稿时长
64 days
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