Cumulative burden of inflammation predicts colorectal neoplasia risk in ulcerative colitis: a large single-centre study

• Published in: Gut Vol. 68; no. 3; pp. 414 - 422
• Main Authors: Choi, Chang-Ho Ryan, Al Bakir, Ibrahim, Ding, Nik-Sheng (John), Lee, Gui-Han, Askari, Alan, Warusavitarne, Janindra, Moorghen, Morgan, Humphries, Adam, Ignjatovic-Wilson, Ana, Thomas-Gibson, Siwan, Saunders, Brian P, Rutter, Matthew D, Graham, Trevor A, Hart, Ailsa L
• Format: Journal Article
• Language: English
• Published: England BMJ Publishing Group LTD 01.03.2019; BMJ Publishing Group
• Series: Original article
• Subjects: Adult; Biopsy; Clinical medicine; Colitis, Ulcerative - complications; Colitis, Ulcerative - pathology; Colon; Colonoscopy; Colorectal cancer; Colorectal Neoplasms - etiology; Endoscopy; Female; Follow-Up Studies; Gastroenterology; Humans; Inflammation; Inflammatory Bowel Disease; Inflammatory bowel diseases; Kaplan-Meier Estimate; Male; Medical screening; Multivariate analysis; Patients; Population Surveillance; Retrospective Studies; Risk Assessment - methods; Risk Factors; Severity of Illness Index; Surveillance; Ulcerative colitis; Young Adult; colorectal neoplasia; colorectal cancer screening; surveillance; inflammation; colonoscopy
• ISSN: 0017-5749; 1468-3288
• DOI: 10.1136/gutjnl-2017-314190

ObjectiveUlcerative colitis (UC) is a dynamic disease with its severity continuously changing over time. We hypothesised that the risk of colorectal neoplasia (CRN) in UC closely follows an actuarial accumulative inflammatory burden, which is inadequately represented by current risk stratification strategies.DesignThis was a retrospective single-centre study. Patients with extensive UC who were under colonoscopic surveillance between 2003 and 2012 were studied. Each surveillance episode was scored for a severity of microscopic inflammation (0=no activity; 1=mild; 2=moderate; 3=severe activity). The cumulative inflammatory burden (CIB) was defined as sum of: average score between each pair of surveillance episodes multiplied by the surveillance interval in years. Potential predictors were correlated with CRN outcome using time-dependent Cox regression.ResultsA total of 987 patients were followed for a median of 13 years (IQR, 9-18), 97 (9.8%) of whom developed CRN. Multivariate analysis showed that the CIB was significantly associated with CRN development (HR, 2.1 per 10-unit increase in CIB (equivalent of 10, 5 or 3.3 years of continuous mild, moderate or severe active microscopic inflammation); 95% CI 1.4 to 3.0; P<0.001). Reflecting this, while inflammation severity based on the most recent colonoscopy alone was not significant (HR, 0.9 per-1-unit increase in severity; 95% CI 0.7 to 1.2; P=0.5), a mean severity score calculated from all colonoscopies performed in preceding 5 years was significantly associated with CRN risk (HR, 2.2 per-1-unit increase; 95% CI 1.6 to 3.1; P<0.001).ConclusionThe risk of CRN in UC is significantly associated with accumulative inflammatory burden. An accurate CRN risk stratification should involve assessment of multiple surveillance episodes to take this into account.