Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34874
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dc.contributor.authorShah, Ayesha-
dc.contributor.authorJones, Michael P-
dc.contributor.authorCallaghan, Gavin-
dc.contributor.authorFairlie, Thomas-
dc.contributor.authorMa, Xiaomin-
dc.contributor.authorCulver, Emma L-
dc.contributor.authorStuart, Katherine-
dc.contributor.authorDe Cruz, Peter P-
dc.contributor.authorO'Beirne, James-
dc.contributor.authorTabibian, James H-
dc.contributor.authorDignass, Axel-
dc.contributor.authorCanbay, Ali-
dc.contributor.authorGores, Gregory J-
dc.contributor.authorHoltmann, Gerald J-
dc.date2024-
dc.date.accessioned2024-01-19T05:25:06Z-
dc.date.available2024-01-19T05:25:06Z-
dc.date.issued2024-01-01-
dc.identifier.citationHepatology Communications 2024-01-01; 8(1)en_US
dc.identifier.issn2471-254X-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34874-
dc.description.abstractPrimary sclerosing cholangitis (PSC) is an immune-mediated, chronic cholestatic liver disease. Currently, liver transplantation is the only established life-saving treatment. Several studies have evaluated the effect of different biologic therapies on PSC with inconclusive findings. We conducted a systematic review and meta-analysis to assess the effects of biologics in PSC and associated inflammatory bowel disease (IBD). MEDLINE, Scopus, and Embase were searched up to July 31, 2023, for studies reporting the effects of biologics in patients with PSC-IBD. Effects of biologic therapy on alkaline phosphatase, total bilirubin, ulcerative colitis response score, and adverse events were calculated and expressed as standardized difference of means (SMD), proportions, and 95% CI using a random-effects model. Six studies, including 411 PSC-IBD patients who received biologics, were included. Biologic treatment was associated with no change in alkaline phosphatase (SMD: 0.1, 95% CI: -0.07 -0.17, p=0.43), but a small and statistically significant increase in total bilirubin (SMD: 0.2, 95% CI: 0.05-0.35, p<0.01). 31.2% (95% CI: 23.8-39.7) of patients with IBD achieved endoscopic response, and there was a significant improvement in ulcerative colitis response score (SMD: -0.6,95% CI: -0.88 to 0.36, p<0.01). Furthermore, 17.6% (95% CI: 13.0-23.5) of patients experienced adverse events severe enough to discontinue therapy, and 29.9% (95% CI: 25.2-34.8) had a loss of response to biologics. Treatment of patients with PSC-IBD with biologics (vedolizumab, infliximab, and adalimumab) was not associated with improvement of biochemical markers of cholestasis. Biologics are effective in treating the colitis associated with PSC. Vedolizumab was associated with worsening liver enzymes in contrast to other biologics, a finding that warrants further study.en_US
dc.language.isoeng-
dc.titleEfficacy and safety of biologics in primary sclerosing cholangitis with inflammatory bowel disease: A systematic review and meta-analysis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleHepatology Communicationsen_US
dc.identifier.affiliationThe University of Queensland, Faculty of Medicine, Australia.;Department of Gastroenterology & Hepatology, Princess Alexandra Hospital.;Translational Research Institute, Queensland, Australia.;AGIRA (Australian Gastrointestinal Research Alliance) and the NHMRC Centre of Research Excellence in Digestive Health.en_US
dc.identifier.affiliationAGIRA (Australian Gastrointestinal Research Alliance) and the NHMRC Centre of Research Excellence in Digestive Health.;Department of Psychology, Macquarie University, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Gastroenterology & Hepatology, Princess Alexandra Hospital.en_US
dc.identifier.affiliationThe University of Queensland, Faculty of Medicine, Australia.;Department of Gastroenterology & Hepatology, Princess Alexandra Hospital.;Translational Research Institute, Queensland, Australia.;AGIRA (Australian Gastrointestinal Research Alliance) and the NHMRC Centre of Research Excellence in Digestive Health.en_US
dc.identifier.affiliationThe University of Queensland, Faculty of Medicine, Australia.;Department of Gastroenterology & Hepatology, Princess Alexandra Hospital.en_US
dc.identifier.affiliationTranslational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.;NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United Kingdom.en_US
dc.identifier.affiliationThe University of Queensland, Faculty of Medicine, Australia.;Department of Gastroenterology & Hepatology, Princess Alexandra Hospital.en_US
dc.identifier.affiliationGastroenterology and Hepatologyen_US
dc.identifier.affiliationUniversity of the Sunshine Coast, Sunshine Coast, Queensland, Australia.;Sunshine Coast University Hospital, Sunshine Coast, Queensland, Australia.en_US
dc.identifier.affiliationDavid Geffen School of Medicine at UCLA, Los Angeles, California, USA.en_US
dc.identifier.affiliationDepartment of Medicine I, Agaplesion Markus Hospital, Frankfurt, Germany.en_US
dc.identifier.affiliationDepartment of Medicine, University Hospital of the Ruhr-University Bochum, Germany.en_US
dc.identifier.affiliationDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.en_US
dc.identifier.affiliationThe University of Queensland, Faculty of Medicine, Australia.;Department of Gastroenterology & Hepatology, Princess Alexandra Hospital.;Translational Research Institute, Queensland, Australia.;AGIRA (Australian Gastrointestinal Research Alliance) and the NHMRC Centre of Research Excellence in Digestive Health.en_US
dc.identifier.doi10.1097/HC9.0000000000000347en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-0710-1691en_US
dc.identifier.orcid0000-0002-0206-2358en_US
dc.identifier.pubmedid38206197-
dc.description.volume8-
dc.description.issue1-
dc.subject.meshtermssecondaryColitis, Ulcerative/drug therapy-
dc.subject.meshtermssecondaryCholangitis, Sclerosing/complications-
dc.subject.meshtermssecondaryCholangitis, Sclerosing/drug therapy-
dc.subject.meshtermssecondaryInflammatory Bowel Diseases/complications-
dc.subject.meshtermssecondaryInflammatory Bowel Diseases/drug therapy-
dc.subject.meshtermssecondaryBiological Products/adverse effects-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptGastroenterology and Hepatology-
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