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Biomarkers for Monitoring of Changes in Disease Activity in Ulcerative Colitis

医学 钙蛋白酶 溃疡性结肠炎 生物标志物 胃肠病学 内科学 抗体 C反应蛋白 英夫利昔单抗 疾病 炎症性肠病 免疫学 炎症 生物化学 化学
作者
Yoshihiro Tatsumi,Kazuki Kakimoto,Azusa Hara,Noboru Mizuta,Keijiro Numa,Naohiko Kinoshita,Kôzô Nakazawa,Ryoji Koshiba,Yuki Hirata,Ota K,Takako Miyazaki,Shirô Nakamura,Kayoko Sakagami,Shoko Arimitsu,Hiroaki Ito,Hiroki Nishikawa
出处
期刊:Journal of Clinical Medicine [Multidisciplinary Digital Publishing Institute]
卷期号:12 (22): 7165-7165
标识
DOI:10.3390/jcm12227165
摘要

In recent years, various biomarkers of ulcerative colitis (UC) have emerged; however, few studies have simultaneously examined the utility of multiple biomarkers for monitoring disease activity. Additionally, serum leucine-rich alpha-2 glycoprotein (LRG), a new biomarker, may show a blunt response to anti-TNF antibody therapy. This prospective study explored effective biomarkers that could monitor disease activity changes in patients with UC. In addition, we examined the effect of anti-TNF antibody therapy on changes in LRG.Blood and stool samples were collected twice from patients with UC: at baseline and at least 8 weeks later. Changes in serum LRG, interleukin (IL)-6, prealbumin (pre-Alb), high-sensitivity C-reactive protein (hs-CRP), CRP, and fecal calprotectin (FC) were measured and correlated with changes in disease activity. The relationship between anti-TNF antibody therapy and LRG levels was also examined in patients with the same disease activity.Forty-eight patients with UC (96 samples) were analyzed. ΔLRG and ΔIL-6 correlated strongly with the change in the partial Mayo (pMayo) score between the two time points (ΔpMayo) (r = 0.686, 0.635, respectively). In contrast, FC and IL-6 were particularly accurate predictors of clinical remission, and their area under the curves (AUCs) were significantly higher than that of CRP (AUC: 0.81, 0.76 vs. 0.50; p = 0.001, 0.005). No association was found between the administration of anti-TNF antibody preparations and the LRG values.Correlations were found between changes in UC disease activity and LRG, IL-6, pre-Alb, hs-CRP, CRP, and FC. LRG reflects disease activity during anti-TNF antibody therapy.

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