Systematic Review and Meta-Analysis of Inflammatory Bowel Disease Adverse Events with Anti-Interleukin 17A Agents and Tumor Necrosis Factor Inhibitors in Rheumatic Disease and Skin Psoriasis
| dc.contributor.author | Truong, Steven L. | |
| dc.contributor.author | Chin, Jasmine | |
| dc.contributor.author | Liew, David F. L. | |
| dc.contributor.author | Zahir, Syeda Farah | |
| dc.contributor.author | Ryan, Elizabeth G. | |
| dc.contributor.author | Rubel, Diana | |
| dc.contributor.author | Radford-Smith, Graham | |
| dc.contributor.author | Robinson, Philip C. | |
| dc.date.accessioned | 2024-02-26T03:16:27Z | |
| dc.date.available | 2024-02-26T03:16:27Z | |
| dc.date.issued | 2021 | |
| dc.date.updated | 2022-10-09T07:17:13Z | |
| dc.description.abstract | Introduction The aim of this work is to perform a systematic review and meta-analysis of anti-tumor necrosis factor (anti-TNF) and anti-interleukin-17 (anti-IL-17) trials for spondyloarthritis, psoriatic arthritis, and psoriasis comparing rates of inflammatory bowel disease (IBD) events compared to placebo. Methods MEDLINE, EMBASE, and The Cochrane Library were searched for double-blind, randomized placebo-controlled anti-TNF and anti-IL-17 trials of included diseases. Inflammatory bowel disease events from the RCT period were pooled and meta-analyzed using statistical methods suitable for low-event-rate meta-analysis (Peto’s, Mantel–Haenszel, hypergeometric-normal model, and Shuster-Guo-Skyler). When observed data were insufficient, we performed an exploratory sensitivity analysis to compare methods. Results We identified 9551 original papers, and included 96 publications: 65 anti-TNF and 31 anti-IL-17 trials, containing 21 new and 12 flare IBD events in 28,209 participants. New IBD on anti-IL-17 occurred 0.23/100 patient-years (PY) in psoriasis, 0.61/100 PY in PsA and 1.63/100 PY in spondyloarthritis, rates similar to observational cohorts, and less commonly on anti-TNF (0/100 PY, 0/100 PY, 0.32/100 PY, respectively). No evidence of difference between groups was found, with wide CI from many pooled counts of zero, especially in placebo arms. Conclusions IBD events were rare, occurring at rates similar to biologic-naive groups. We could not find statistically significant differences in risk of new or recurrent IBD between treatment and control groups using selected meta-analytical methods for low event rate scenarios. Meta-analyses of this topic require more IBD events, ideally without pooling heterogeneous groups. Larger, thoroughly reported trials with systematic and detailed safety reporting are required to improve risk estimation and to make accurate inferences. | en_AU |
| dc.description.sponsorship | This work was supported by an unrestricted grant from Novartis Pharmaceuticals Australia. This funding paid for investigator time, statistical analysis, and the journal’s Rapid Service Fee. | en_AU |
| dc.format.mimetype | application/pdf | en_AU |
| dc.identifier.issn | 2198-6584 | en_AU |
| dc.identifier.uri | http://hdl.handle.net/1885/313912 | |
| dc.language.iso | en_AU | en_AU |
| dc.provenance | This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/. | en_AU |
| dc.publisher | Adis International Ltd. | en_AU |
| dc.rights | © 2021 The authors | en_AU |
| dc.rights.license | Creative Commons Attribution licence | en_AU |
| dc.rights.uri | http://creativecommons.org/licenses/ by-nc/4.0/ | en_AU |
| dc.source | Rheumatology and Therapy | en_AU |
| dc.subject | Inflammatory bowel disease | en_AU |
| dc.subject | Antiinterleukin-17 | en_AU |
| dc.subject | Anti-tumor necrosis factor | en_AU |
| dc.subject | Axial spondyloarthritis | en_AU |
| dc.subject | Psoriatic arthritis | en_AU |
| dc.subject | Psoriasis | en_AU |
| dc.subject | Meta-analysis | en_AU |
| dc.subject | Crohn’s disease | en_AU |
| dc.subject | Ulcerative colitis | en_AU |
| dc.subject | Pharmacovigilance | en_AU |
| dc.title | Systematic Review and Meta-Analysis of Inflammatory Bowel Disease Adverse Events with Anti-Interleukin 17A Agents and Tumor Necrosis Factor Inhibitors in Rheumatic Disease and Skin Psoriasis | en_AU |
| dc.type | Journal article | en_AU |
| dcterms.accessRights | Open Access | en_AU |
| local.bibliographicCitation.lastpage | 1616 | en_AU |
| local.bibliographicCitation.startpage | 1603 | en_AU |
| local.contributor.affiliation | Truong, Steven L., Griffith University | en_AU |
| local.contributor.affiliation | Chin, Jasmine, University of Queensland | en_AU |
| local.contributor.affiliation | Liew, David F. L., University of Melbourne | en_AU |
| local.contributor.affiliation | Zahir, Syeda Farah, University of Queensland | en_AU |
| local.contributor.affiliation | Ryan, Elizabeth G., University of Queensland | en_AU |
| local.contributor.affiliation | Rubel, Diana, College of Health and Medicine, ANU | en_AU |
| local.contributor.affiliation | Radford-Smith, Graham, University of Queensland | en_AU |
| local.contributor.affiliation | Robinson, Philip C., University of Queensland | en_AU |
| local.contributor.authoruid | Rubel, Diana, u5458435 | en_AU |
| local.description.notes | Imported from ARIES | en_AU |
| local.identifier.absfor | 320223 - Rheumatology and arthritis | en_AU |
| local.identifier.absfor | 320402 - Applied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies) | en_AU |
| local.identifier.ariespublication | a383154xPUB22244 | en_AU |
| local.identifier.citationvolume | 8 | en_AU |
| local.identifier.doi | 10.1007/s40744-021-00360-6 | en_AU |
| local.identifier.scopusID | 2-s2.0-85113632236 | |
| local.identifier.thomsonID | WOS:000690333300001 | |
| local.publisher.url | https://link.springer.com/ | en_AU |
| local.type.status | Published Version | en_AU |
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