Serum Zonulin Measured by Commercial Kit Fails to Correlate With Physiologic Measures of Altered Gut Permeability in First Degree Relatives of Crohn's Disease Patients

The CCC GEM Project Research Consortium

Résultat de recherche: Articleexamen par les pairs

19 Citations (Scopus)

Résumé

Intestinal epithelial cell tight junctions (TJs) contribute to the integrity of the intestinal barrier allowing for control of the physical barrier between external antigens or bacterial products and the internal environment. Zonula occludens-1 (ZO-1) is a protein that modulates intestinal TJs, and serum levels of ZO-1 has been suggested as a biomarker of disrupted barrier function in humans. Previous studies suggested that increased intestinal permeability was associated with evidence of TJ abnormalities. However, there is limited information on the serological measurement of ZO-1 and its relation to other tests of barrier function in healthy subjects. We investigated the correlation of serum ZO-1, with physiologic measures of intestinal permeability (as the ratio of the fractional excretion of lactulose-mannitol or LMR) in a cohort of 39 healthy FDRs of Crohn's disease (CD) patients. No significant correlation was found between LMR and ZO-1 levels (r2 = 0.004, P < 0.71), or intestinal fatty acid binding proteins (I-FABP) (r2 = 0.004, P < 0.71). In conclusion, our data show that ZO-1 and I-FABP are not a marker of gut permeability as defined by LMR.

Langue d'origineEnglish
Numéro d'article645303
JournalFrontiers in Physiology
Volume12
DOI
Statut de publicationPublished - mars 25 2021

Note bibliographique

Funding Information:
We thank Kevin Ow, Ashleigh Goethel, Heather MacAulay, and everyone in the members of the CCC GEM Global Project Office. Funding. This study was supported by grants from Crohn's and Colitis Canada (Grant No. CCC-GEMIII), Canadian Institutes of Health Research (CIHR) (Grant No. CMF108031), and the Helmsley Charitable Trust. KC was partially supported by a Canada Research Chair in Inflammatory Bowel Diseases. WT was a former recipient of a Post-doctoral Fellowship Research Award from the CIHR Fellowship/Canadian Association of Gastroenterology/Ferring Pharmaceuticals Inc. and a recipient of a fellowship from the Department of Medicine, Mount Sinai Hospital, Toronto, Canada.

Funding Information:
This study was supported by grants from Crohn’s and Colitis Canada (Grant No. CCC-GEMIII), Canadian Institutes of Health Research (CIHR) (Grant No. CMF108031), and the Helmsley Charitable Trust. KC was partially supported by a Canada Research Chair in Inflammatory Bowel Diseases. WT was a former recipient of a Postdoctoral Fellowship Research Award from the CIHR Fellowship/Canadian Association of Gastroenterology/Ferring Pharmaceuticals Inc. and a recipient of a fellowship from the Department of Medicine, Mount Sinai Hospital, Toronto, Canada.

Publisher Copyright:
© Copyright © 2021 Power, Turpin, Espin-Garcia, Smith, The CCC GEM Project Research Consortium and Croitoru.

ASJC Scopus Subject Areas

  • Physiology
  • Physiology (medical)

PubMed: MeSH publication types

  • Journal Article

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