Sawahashi Motoi, Kakuta Yoichi, Naito Takeo, Okazaki Soshi, Ohneda Kinuko, Orui Masatsugu, Obara Taku, Ogishima Soichi, Kumada Kazuki, Kudo Hisaaki, Nagami Fuji, Hozawa Atsushi, Iwaki Hideya, Nagai Hiroshi, Shimoyama Yusuke, Moroi Rintaro, Shiga Hisashi, Kinouchi Yoshitaka, Shirai Tsuyoshi, Fujii Hiroshi, Masamune Atsushi
Division of Gastroenterology, Tohoku University Graduate School of Medicine, 1-1, Seiryo, Aoba-Ku, Sendai, Miyagi, 980-8574, Japan.
Department of Rheumatology, Tohoku University Hospital, Sendai, Japan.
J Gastroenterol. 2025 May 15. doi: 10.1007/s00535-025-02263-7.
A method for predicting ulcerative colitis (UC) onset has not been established. Serum autoantibodies have been suggested as potential predictive biomarkers for UC onset. We aimed to validate the risks associated with serological and environmental factors and construct a model for predicting UC development.
Using the population-based cohort studies (n > 83,000), we identified 42 individuals who were diagnosed with UC later in life and compared them with matched healthy controls. We analyzed serum anti-integrin αvβ6 antibody (anti-αvβ6) and anti-endothelial protein C receptor antibody (anti-EPCR) titers, and lifestyle and dietary habits to explore UC onset predictors. The predictive performance of the models was evaluated based on these predictors.
The sensitivity and specificity of anti-EPCR for predicting UC onset were 51.4% and 97.8%, respectively, comparable to those of anti-αvβ6 (52.5% and 97.6%, respectively). The proportion of individuals with insomnia was significantly higher in the preclinical UC group (adjusted odds ratio = 2.14, 95% confidence interval [CI] 1.11-4.04, p = 0.019). The predictive performance of anti-EPCR alone was high with an area under the curve (AUC) of 0.89 (95%CI 0.83-0.96), and that of anti-EPCR combined with anti-αvβ6 was even better with an AUC of 0.92 (95%CI 0.87-0.97); the lifestyle model had lower predictive accuracy (AUC = 0.65, 95%CI 0.55-0.74).
Anti-EPCR and anti-αvβ6 each strongly predict UC onset. The combined anti-EPCR and anti-αvβ6 model had stronger predictive performance than the single models.
尚未建立预测溃疡性结肠炎(UC)发病的方法。血清自身抗体被认为是UC发病的潜在预测生物标志物。我们旨在验证与血清学和环境因素相关的风险,并构建一个预测UC发展的模型。
利用基于人群的队列研究(n>83000),我们确定了42名在晚年被诊断为UC的个体,并将他们与匹配的健康对照进行比较。我们分析了血清抗整合素αvβ6抗体(抗αvβ6)和抗内皮蛋白C受体抗体(抗EPCR)滴度,以及生活方式和饮食习惯,以探索UC发病的预测因素。基于这些预测因素评估模型的预测性能。
抗EPCR预测UC发病的敏感性和特异性分别为51.4%和97.8%,与抗αvβ6相当(分别为52.5%和97.6%)。临床前UC组失眠个体的比例显著更高(调整优势比=2.14,95%置信区间[CI]1.11-4.04,p=0.019)。单独抗EPCR的预测性能较高,曲线下面积(AUC)为0.89(95%CI 0.83-0.96),抗EPCR与抗αvβ6联合使用时预测性能更好,AUC为0.92(95%CI 0.87-0.97);生活方式模型的预测准确性较低(AUC=0.65,95%CI 0.55-0.74)。
抗EPCR和抗αvβ6均可强烈预测UC发病。抗EPCR和抗αvβ6联合模型的预测性能比单一模型更强。