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Efficacy and predictor of anti-TNFα agents in patients with intestinal Behçet's disease

dc.contributor.authorMiyazaki, Haruka
dc.contributor.authorWatanabe, Daisuke
dc.contributor.authorOkamoto, Norihiro
dc.contributor.authorTokunaga, Eri
dc.contributor.authorKu, Yuna
dc.contributor.authorTakenaka, Haruka
dc.contributor.authorHoshi, Namiko
dc.contributor.authorOoi, Makoto
dc.contributor.authorKodama, Yuzo
dc.date.accessioned2022-08-10T18:10:56Z
dc.date.available2022-08-10T18:10:56Z
dc.date.issued2022-03-28
dc.identifier.citationBMC Gastroenterology. 2022 Mar 28;22(1):149
dc.identifier.urihttps://doi.org/10.1186/s12876-022-02221-0
dc.identifier.urihttps://hdl.handle.net/2027.42/173563en
dc.description.abstractAbstract Background Behçet’s disease (BD) is a recurrent multisystem inflammatory disease. Anti-tumor necrosis factor (TNF) α agents have been used to treat patients with intestinal BD with severe disease activity or those who are resistant to conventional treatments; however, the long-term efficacy of anti-TNFα agents in intestinal BD remains unclear. In the present study, we investigated the clinical outcomes and predictors of discontinuation of anti-TNFα agents in patients with intestinal BD. Methods We reviewed the medical records of patients with intestinal BD who received first-line anti-TNFα agents between January 2009 and June 2020. The primary outcome was the percentage of patients who continued anti-TNFα therapy for 48 weeks. Secondary outcomes included the percentage of patients who achieved marked improvement, complete remission, and mucosal healing, as well as predictors of discontinuation of anti-TNFα agents. Results A total of 29 patients were included in the study. Twenty-two (75.9%) patients continued anti-TNFα therapy for 48 weeks. The percentage of patients who achieved marked improvement, complete remission, and mucosal healing at week 48 was 48.3%, 37.9%, and 48.3%, respectively. At week 96, 11 (37.9%) patients achieved marked improvement, complete remission, and mucosal healing. A higher C-reactive protein level (CRP; ≥ 1 mg/dL) at baseline was a predictor of discontinuation of anti-TNFα agents. Conclusions The 48-week continuation rate of anti-TNFα agents was 75.9% in bio-naïve patients with intestinal BD. However, a higher baseline CRP level (≥ 1 mg/dL) was associated with discontinuation of anti-TNFα agents.
dc.titleEfficacy and predictor of anti-TNFα agents in patients with intestinal Behçet's disease
dc.typeJournal Article
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/173563/1/12876_2022_Article_2221.pdf
dc.identifier.doihttps://dx.doi.org/10.7302/5294
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.date.updated2022-08-10T18:10:55Z
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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