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Anti-integrin αvβ6 antibody as a biomarker for diagnosing ulcerative colitis: a nationwide multicenter validation study

医学 溃疡性结肠炎 内科学 生物标志物 胃肠病学 逻辑回归 队列研究 肝病学 外科肿瘤学 炎症性肠病 试验预测值 前瞻性队列研究 疾病 生物化学 化学
作者
Makoto Okabe,Shuji Yamamoto,M. Shiokawa,Tadakazu Hisamatsu,Hajime Yamazaki,Risa Nakanishi,K Hamada,Hiroki Kitamoto,Takeshi Kuwada,Norimitsu Uza,Aki Sakatani,Toshimitsu Fujii,Masashi Ohno,Minoru Matsuura,Tomoyoshi Shibuya,Naoki Ohmiya,Makoto Ooi,Namiko Hoshi,Kei Moriya,Kiichiro Tsuchiya
出处
期刊:Journal of Gastroenterology [Springer Nature]
卷期号:60 (1): 86-95
标识
DOI:10.1007/s00535-024-02176-x
摘要

Abstract Background A serum biomarker for diagnosing ulcerative colitis (UC) remains to be established. Although we recently reported an anti-integrin αvβ6 antibody (V6 Ab) for diagnosing UC with high sensitivity and specificity, no large-scale validation study exists. This study aimed to validate the diagnostic value of V6 Ab for UC using a nationwide multicenter cohort study. Methods We measured V6 Ab titers in patients definitively diagnosed with UC, Crohn’s disease (CD), or other gastrointestinal disorders (OGDs). The primary outcome was the diagnostic value of V6 Ab. Secondary outcomes were factors associated with false-negative results in patients with UC and false-positive results in patients without UC and the heterogeneity of the diagnostic value of V6 Ab among the participating facilities. Results We enrolled 1241, 796, and 206 patients with UC, CD, and OGD, respectively, from 28 Japanese high-volume referral centers. The diagnostic sensitivity of V6 Ab for UC was 87.7%, and its specificities for CD and OGDs were 82.0% and 87.4%, respectively. Multivariable logistic regression analysis showed that false-negative results were associated with older age at the time of sample collection, current smokers, lower partial Mayo score, and not receiving advanced therapies in patients with UC, and false-positive results were associated with colonic CD in patients with CD. No factor was associated with false-positive results in patients with OGDs. There were no significant differences in the diagnostic value of V6 Ab among the centers. Conclusions The diagnostic value of V6 Ab for UC was validated in the large-scale nationwide multicenter study.

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