钙蛋白酶
胃肠病学
溃疡性结肠炎
医学
结肠镜检查
内科学
炎症性肠病
前瞻性队列研究
粪便
结肠炎
代理终结点
疾病
结直肠癌
癌症
生物
古生物学
作者
Gustavo Drügg Hahn,Péter L. Lakatos,Chelsea Maedler‐Kron,Victoria Marcus,Waqqas Afif,Gary Wild,Alain Bitton,Cristina Flores,Carlos Fernando de Magalhães Francesconi,Talat Bessissow
摘要
Abstract Background Fecal calprotectin is a reliable surrogate marker for disease activity in ulcerative colitis. However, there are no consensus cutoff values for histoendoscopic remission. This study aimed to correlate fecal calprotectin with Mayo endoscopic score and histological disease activity (Geboes score) for ulcerative colitis patients in clinical remission. Methods Prospective study including adult ulcerative colitis patients in clinical remission or disease relapse, undergoing endoscopy for disease activity or dysplasia surveillance at an inflammatory bowel disease center between 2013 and 2020. Fecal calprotectin was collected before bowel preparation and Mayo endoscopic score was documented during colonoscopy. Biopsies were taken throughout the colon and histological activity was assessed using Geboes score by a blinded expert gastrointestinal pathologist. Results Two hundred fifty-three patients were included, 117 (46%) were male (mean age of 38.2 years—standard deviation ± 24.8). A fecal calprotectin ≥ 123 μg/g predicts Mayo endoscopic score > 0 (58% sensitivity and 70% specificity), also aiding to differentiate Mayo endoscopic score 0 from 1 (61% sensitivity and 70% specificity). A fecal calprotectin ≥ 80 μg/g identified histological disease activity using Geboes score > 3.1 in patients with clinical remission (64.7% sensitivity, 58.7% specificity). Using Geboes score > 2, a fecal calprotectin ≥ 50 μg/g, is the most clinically relevant to identify patients in clinical remission with active histologic inflammation (49.6% sensitivity, 41.6% specificity). Conclusions Fecal calprotectin correlates with endoscopic and histologic disease activity and can be used as a surrogate marker for disease activity. Our study prospectively demonstrated optimal cutoff values to discriminate histoendoscopic remission.
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