Soluble Syndecan-1: A Novel Biomarker of Small Bowel Mucosal Damage in Children with Celiac Disease

Background Syndecan-1 (SDC1) is essential for maintaining normal epithelial barrier. Shedding of SDC1 ectodomain, reflected by serum soluble syndecan-1 ( S SDC1) levels, is regulated by inflammation. Increased intestinal permeability plays a central role in celiac disease (CD). The association betwe...

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Veröffentlicht in:Digestive diseases and sciences 2017-03, Vol.62 (3), p.755-760
Hauptverfasser: Yablecovitch, D., Oren, A., Ben-Horin, S., Fudim, E., Eliakim, R., Saker, T., Konikoff, F. M., Kopylov, U., Matthias, T., Lerner, A.
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Sprache:eng
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Zusammenfassung:Background Syndecan-1 (SDC1) is essential for maintaining normal epithelial barrier. Shedding of SDC1 ectodomain, reflected by serum soluble syndecan-1 ( S SDC1) levels, is regulated by inflammation. Increased intestinal permeability plays a central role in celiac disease (CD). The association between S SDC1 levels and mucosal damage in CD has not been evaluated. Aims To evaluate serum S SDC1 levels in children with CD and to determine its relationship with histological grading classified by modified Marsh criteria. Methods This is a cross-sectional, pilot study, in which serum S SDC1 was analyzed by ELISA in a cohort of 49 untreated children with CD and 15 children with nonspecific abdominal pain (AP). CD was diagnosed based on positive celiac serology and small intestinal biopsy. S SDC1 levels at the time of biopsy were correlated with Marsh grading. Controls were defined by AP, negative celiac serology, normal upper endoscopy, and small intestinal biopsies. Results S SDC1 levels were significantly higher in CD patients compared to AP controls (116.2 ± 161 vs. 41.3 ± 17.5 ng/ml, respectively, p  
ISSN:0163-2116
1573-2568
DOI:10.1007/s10620-016-4415-8