医学
内科学
自身抗体
胃肠病学
优势比
溃疡性结肠炎
置信区间
内皮蛋白C受体
曲线下面积
人口
血清学
免疫学
抗体
疾病
血小板
环境卫生
凝血酶
作者
Motoi Sawahashi,Yoichi Kakuta,Takeo Naito,Soshi Okazaki,Kinuko Ohneda,Masatsugu Orui,Taku Obara,Soichi Ogishima,Kazuki Kumada,Hisaaki Kudo,Fuji Nagami,Atsushi Hozawa,Hideya Iwaki,Hiroshi Nagai,Yusuke Shimoyama,Rintaro Moroi,Hisashi Shiga,Yoshitaka Kinouchi,Tsuyoshi Shirai,Hiroshi Fujii
标识
DOI:10.1007/s00535-025-02263-7
摘要
BACKGROUND: 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. METHODS: 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. RESULTS: 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). CONCLUSIONS: 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.
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