4.8 Article

Increased Intestinal Permeability Is Associated With Later Development of Crohn 's Disease

Journal

GASTROENTEROLOGY
Volume 159, Issue 6, Pages -

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2020.08.005

Keywords

FDR Study; IBD; Gut Barrier; Crohn's Risk

Funding

  1. Crohn's and Colitis Canada [CCC-GEMIII]
  2. Canadian Institutes of Health Research (CIHR) [CMF108031]
  3. Helmsley Charitable Trust
  4. CIHR Fellowship/Canadian Association of Gastroenterology/Ferring Pharmaceuticals Inc.
  5. Department of Medicine, Mount Sinai Hospital, Toronto, Canada
  6. Canada Research Chair in Immune-Mediated Gastrointestinal Disorders
  7. Bruce Kaufman Chair in Inflammatory Bowel Disease at McGill
  8. Canada Research Chair in Inflammatory Bowel Diseases

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BACKGROUND & AIMS: Increased intestinal permeability has been associated with Crohn's disease (CD), but it is not clear whether it is a cause or result of the disease. We performed a prospective study to determine whether increased intestinal permeability is associated with future development of CD. METHODS: We assessed the intestinal permeability, measured by the urinary fractional excretion of lactulose-to-mannitol ratio (LMR) at recruitment in 1420 asymptomatic first-degree relatives (6-35 years old) of patients with CD (collected from 2008 through 2015). Participants were then followed up for a diagnosis of CD from 2008 to 2017, with a median follow-up time of 7.8 years. We analyzed data from 50 participants who developed CD after a median of 2.7 years during the study period, along with 1370 individuals who remained asymptomatic until October 2017. We used the Cox proportional hazards model to evaluate time-related risk of CD based on the baseline LMR. RESULTS: An abnormal LMR (>0.03) was associated with a diagnosis of CD during the follow-up period(hazard ratio, 3.03; 95% CI, 1.64-5.63; P = 3.97 x 10(-4)). This association remained significant even when the test was performed more than 3 years before the diagnosis of CD (hazard ratio, 1.62; 95% CI, 1.051-2.50; P = .029). CONCLUSIONS: Increased intestinal permeability is associated with later development of CD; these findings support a model in which altered intestinal barrier function contributes to pathogenesis. Abnormal gut barrier function might serve as a biomarker for risk of CD onset.

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