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.authorTruong, Steven L.
dc.contributor.authorChin, Jasmine
dc.contributor.authorLiew, David F. L.
dc.contributor.authorZahir, Syeda Farah
dc.contributor.authorRyan, Elizabeth G.
dc.contributor.authorRubel, Diana
dc.contributor.authorRadford-Smith, Graham
dc.contributor.authorRobinson, Philip C.
dc.date.accessioned2024-02-26T03:16:27Z
dc.date.available2024-02-26T03:16:27Z
dc.date.issued2021
dc.date.updated2022-10-09T07:17:13Z
dc.description.abstractIntroduction 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.sponsorshipThis 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.mimetypeapplication/pdfen_AU
dc.identifier.issn2198-6584en_AU
dc.identifier.urihttp://hdl.handle.net/1885/313912
dc.language.isoen_AUen_AU
dc.provenanceThis 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.publisherAdis International Ltd.en_AU
dc.rights© 2021 The authorsen_AU
dc.rights.licenseCreative Commons Attribution licenceen_AU
dc.rights.urihttp://creativecommons.org/licenses/ by-nc/4.0/en_AU
dc.sourceRheumatology and Therapyen_AU
dc.subjectInflammatory bowel diseaseen_AU
dc.subjectAntiinterleukin-17en_AU
dc.subjectAnti-tumor necrosis factoren_AU
dc.subjectAxial spondyloarthritisen_AU
dc.subjectPsoriatic arthritisen_AU
dc.subjectPsoriasisen_AU
dc.subjectMeta-analysisen_AU
dc.subjectCrohn’s diseaseen_AU
dc.subjectUlcerative colitisen_AU
dc.subjectPharmacovigilanceen_AU
dc.titleSystematic 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 Psoriasisen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.lastpage1616en_AU
local.bibliographicCitation.startpage1603en_AU
local.contributor.affiliationTruong, Steven L., Griffith Universityen_AU
local.contributor.affiliationChin, Jasmine, University of Queenslanden_AU
local.contributor.affiliationLiew, David F. L., University of Melbourneen_AU
local.contributor.affiliationZahir, Syeda Farah, University of Queenslanden_AU
local.contributor.affiliationRyan, Elizabeth G., University of Queenslanden_AU
local.contributor.affiliationRubel, Diana, College of Health and Medicine, ANUen_AU
local.contributor.affiliationRadford-Smith, Graham, University of Queenslanden_AU
local.contributor.affiliationRobinson, Philip C., University of Queenslanden_AU
local.contributor.authoruidRubel, Diana, u5458435en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor320223 - Rheumatology and arthritisen_AU
local.identifier.absfor320402 - Applied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies)en_AU
local.identifier.ariespublicationa383154xPUB22244en_AU
local.identifier.citationvolume8en_AU
local.identifier.doi10.1007/s40744-021-00360-6en_AU
local.identifier.scopusID2-s2.0-85113632236
local.identifier.thomsonIDWOS:000690333300001
local.publisher.urlhttps://link.springer.com/en_AU
local.type.statusPublished Versionen_AU

Downloads

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
s40744-021-00360-6.pdf
Size:
439.78 KB
Format:
Adobe Portable Document Format
Description: