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首页> 外文期刊>Gut: Journal of the British Society of Gastroenterology >Cumulative burden of inflammation predicts colorectal neoplasia risk in ulcerative colitis: a large single-centre study
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Cumulative burden of inflammation predicts colorectal neoplasia risk in ulcerative colitis: a large single-centre study

机译:炎症的累积负担预测溃疡性结肠炎的结肠直肠肿瘤风险:一个大型单中心研究

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摘要

Ulcerative 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.This 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=noa€‰activity; 1=mild; 2=moderate; 3=severea€‰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.A total of 987 patients were followed for a median of 13 years (IQR, 9a€“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%a€‰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%a€‰CI 0.7 to 1.2; P=0.5), a mean severity score calculated from all colonoscopies performed in preceding 5a€‰years was significantly associated with CRN risk (HR, 2.2 per-1-unit increase; 95%a€‰CI 1.6 to 3.1; P<0.001).The 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.
机译:溃疡性结肠炎(UC)是一种动态疾病,其严重程度随着时间的推移而连续变化。我们假设UC中结肠直肠肿瘤(CRN)的风险紧密遵循精算累积炎症负担,这因当前风险分层策略而言不充分。这是一个回顾性单中心研究。研究了2003年至2012年间结肠透视监测的广泛UC的患者。每个监测发作都被评分为显微镜炎症的严重程度(0 = NOA€‰活性; 1 =温和; 2 =中度; 3 = SEVEEA€‰活动)。累积炎症负担(CIB)被定义为:每对监视剧之间的平均得分乘以多年监测间隔。使用时间依赖的COX回归与CRN结果相关的潜在预测因子。在13年(IQR,9A€“18),97(9.8%)的中位,患者总共持续了987名患者。多变量分析表明,CIB与CRN发育显着相关(HR,每10单位的CIB增加2.1(相当于10,5或3年的连续温和,中等或严重的活性微观炎症); 95%a€‰ci 1.4至3.0; p <0.001)。反映这一点,而仅基于最近的结肠镜检查的炎症严重程度不显着(HR,每1单位的严重程度增加0.9%; 95%A€‰CI0.7至1.2; p = 0.5),从而计算出平均严重性得分前5A欧元的所有结肠镜检查与CRN风险显着相关(HR,2.2每1单位增加; 95%A€CI 1.6至3.1; P <0.001)。UC中CRN的风险显着相关累积炎症负担。准确的CRN风险分层应涉及对多次监控剧集的评估,以考虑到这一点。

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