用于评估克罗恩病肠道损伤的勒曼指数:一项真实世界的研究。

Eric Prado, Cindy C Y Law, Catherine Rowan, Ali Osman, Emily Gore, David H Ballard, Daniel R Ludwig, Richard Tsai, Maté Gergely, Amine Geahchan, Bachir Taouli, Ghadi Abboud, Emre Altinmakas, Palak Rajauria, Jean-Frederic Colombel, Ryan C Ungaro, Parakkal Deepak
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引用次数: 0

摘要

背景与目的:勒曼指数(LI)是衡量克罗恩病(CD)累积性肠道结构损伤的终点,最近已得到更新和验证。我们将其用于研究现实世界队列中的肠损伤预测因素:我们进行了一项回顾性研究(2008-2022 年),涉及美国两家三级 IBD 转诊中心。研究放射科医生对 MR 或 CT 肠道造影进行审查,研究消化科医生对内镜检查报告进行审查,以计算 LI。计算基线和随访 LI。我们将肠道高度损伤定义为 LI ≥2。在LI评分≥2分的患者中,我们使用多变量逻辑回归确定了与高LI相关的因素,然后使用多变量线性混合效应模型评估了LI的变化(增加与不变/减少):结果:447 名 CD 患者的首次 LI 中位数为 7 [IQR,1.25-14.55]。按病程分类,中位LI评分有明显差异;结论为2.0[IQR,0.6-5.9]:更新后的LI量化了CD患者真实世界队列中横断面和纵向累积性肠道损伤,并确定了LI纵向增加的预测因素。需要进一步研究对LI进行前瞻性验证,并确定肠损伤的多组学预测因子。
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Lemann Index for assessing bowel damage in Crohn's disease: a real world study.

Background & aims: The Lemann Index (LI), an endpoint to measure cumulative structural bowel damage in Crohn's disease (CD), has been recently updated and validated. We applied this to investigate predictors of bowel damage in a real-world cohort.

Methods: We performed a retrospective study (2008-2022) involving two tertiary referral IBD centers in the US. MR or CT enterographies were reviewed by study radiologists and endoscopy reports by study gastroenterologists, to calculate LI. Baseline and follow-up LI were calculated. We defined high bowel damage as LI ≥2. Factors associated with high LI were identified in patients with ≥2 LI scores using multivariate logistic regression and then assessed for a change in LI (increase vs. no change/decrease) using a multivariate linear mixed-effects model.

Results: 447 patients with CD had a median first LI of 7 [IQR, 1.25-14.55]. Median LI scores were significantly different when categorized by disease duration; 2.0 [IQR, 0.6-5.9] for <2 years, 2.6 [IQR, 0.6-9.6] for ≥2 and <10 years, and 12.5 [IQR, 6.4-21.5] for ≥10 years with a p <0.01. Disease duration, presence of perianal disease, elevated C-reactive protein, and Harvey-Bradshaw index, were associated with a high LI at inclusion and increase in LI during follow-up (all p <0.01).

Conclusions: The updated LI quantified cross-sectional and longitudinal cumulative bowel damage in a real-world cohort of patients with CD with predictors identified for a longitudinal increase in LI. Further studies for prospective validation of LI and identification of multi-omic predictors of bowel damage are needed.

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