Literature DB >> 29171305

Serum interleukin-6 level is associated with response to infliximab in ulcerative colitis.

Yu Nishida1, Shuhei Hosomi1, Kenji Watanabe1,2, Kimihiko Watanabe1, Tomomi Yukawa1, Koji Otani1, Yasuaki Nagami1, Fumio Tanaka1, Koichi Taira1, Noriko Kamata1, Hirokazu Yamagami1, Tetsuya Tanigawa1, Toshio Watanabe1, Yasuhiro Fujiwara1.   

Abstract

OBJECTIVES: Infliximab is effective in patients with ulcerative colitis (UC); however, one-third of patients do not respond and require additional therapies such as other biologic agents. Therefore, the aim of this study was to analyze the association between pro-inflammatory molecules and clinical efficacy to elucidate possible mechanisms for the non-response to infliximab to aid in treatment selection. MATERIALS AND
METHOD: Patients with moderate-to-severe active UC receiving infliximab in our hospital between 2010 and 2016 for whom pre-treatment serum samples were available were retrospectively evaluated. We analyzed the association between serum interleukin (IL)-6, tumor necrosis factor-α (TNF-α) and soluble mucosal vascular addressin cell adhesion molecule-1 (sMAdCAM-1) and the clinical efficacy of infliximab. The primary endpoint was clinical response at the end of the induction period.
RESULTS: Forty-one patients were included in this study. After induction therapy, 27 patients (65.9%) showed a clinical response. Serum IL-6 levels were significantly lower in responders than in non-responders (p = .012), whereas no significant differences were noted in other factors including sMAdCAM-1 and TNF-α. Multivariate analysis identified that serum IL-6 level (odds ratio = 0.72; 95% confidence interval, 0.54-0.96; p = .027) was independently associated with response to infliximab.
CONCLUSIONS: Serum IL-6 level is associated with response to infliximab in UC. Elevated concentrations of IL-6 may provide insight to the mechanism of non-response to infliximab.

Entities:  

Keywords:  Infliximab; interleukin-6; sMAdCAM; tumor necrosis factor; ulcerative colitis

Mesh:

Substances:

Year:  2017        PMID: 29171305     DOI: 10.1080/00365521.2017.1403647

Source DB:  PubMed          Journal:  Scand J Gastroenterol        ISSN: 0036-5521            Impact factor:   2.423


  7 in total

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