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Supplementary Material for: Anti-IL 12/23 versus Anti-TNF-α in Patients with Biologically Naïve Crohn's Disease: A Systematic Review and Meta-analysis

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DataCite Commons2025-06-06 更新2026-04-25 收录
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https://karger.figshare.com/articles/dataset/Supplementary_Material_for_Anti-IL_12_23_versus_Anti-TNF-_in_Patients_with_Biologically_Na_ve_Crohn_s_Disease_A_Systematic_Review_and_Meta-analysis/29253815
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Background: Crohn’s disease is a chronic inflammatory condition of the digestive tract characterized by a non-continuous pattern of transmural inflammation. This leads to a major decline in quality of life and productivity. For biologic-naïve patients, anti-TNF-α and anti-IL-12/23 therapies are commonly recommended. This study compares anti-IL-12/23 and anti-TNF-α for clinical remission, endoscopic remission, corticosteroid-free remission, and endoscopic response in biologic-naïve patients. Methods: We searched PubMed, Google Scholar, VHL, Cochrane Library, Scopus, Web of Science, and ClinicalTrials.gov for randomized clinical trials and cohort studies. Data were analyzed using odds ratios (OR) with 95% confidence intervals (CI). A random-effects model was applied for meta-analysis. Results: Only 6 out of 5,401 articles were included, involving 1,103 patients. Of these, 636 (57.6%) received anti-TNF-α therapy (infliximab or adalimumab), while 467 (42.4%) received anti-IL-12/23 (ustekinumab) therapy. Within 52 weeks, there were no statistically significant differences found between Ustekinumab and anti-TNF-α in terms of clinical remission (OR: 0.92, 95% CI: 0.55 to 1.54, p-value =0.75), endoscopic remission (OR = 0.583, 95% CI: 0.289–1.176; p = 0.13), corticosteroid-free remission (OR: 1.19, 95% CI: 0.87 to 1.64, p-value = 0.28), or endoscopic response (OR = 0.48, 95% CI: 0.147–1.578; p = 0.23). Conclusion: This meta-analysis found no significant differences in clinical remission, corticosteroid-free remission, endoscopic remission, or endoscopic response within 52 weeks between ustekinumab and anti-TNF-α agents in biologic-naïve CD patients. However, due to study limitations, further high-quality, head-to-head trials are needed to refine treatment selection and optimize outcomes.
提供机构:
Karger Publishers
创建时间:
2025-06-06
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