Literature DB >> 16644703

Zonulin upregulation is associated with increased gut permeability in subjects with type 1 diabetes and their relatives.

Anna Sapone1, Laura de Magistris, Michelle Pietzak, Maria G Clemente, Amit Tripathi, Francesco Cucca, Rosanna Lampis, Deborah Kryszak, Maria Cartenì, Maddalena Generoso, Dario Iafusco, Francesco Prisco, Francesca Laghi, Gabriele Riegler, Romano Carratu, Debra Counts, Alessio Fasano.   

Abstract

Zonulin, a protein that modulates intestinal permeability, is upregulated in several autoimmune diseases and is involved in the pathogenesis of autoimmune diabetes in the BB/Wor animal model of the disease. To verify the association between serum zonulin levels and in vivo intestinal permeability in patients with type 1 diabetes, both parameters were investigated in different stages of the autoimmune process. Forty-two percent (141 of 339) of the patients had abnormal serum zonulin levels, as compared with age-matched control subjects. The increased zonulin levels correlated with increased intestinal permeability in vivo and changes in claudin-1, claudin-2, and myosin IXB genes expression, while no changes were detected in ZO1 and occludin genes expression. When tested in serum samples collected during the pre-type 1 diabetes phase, elevated serum zonulin was detected in 70% of subjects and preceded by 3.5 +/- 0.9 years the onset of the disease in those patients who went on to develop type 1 diabetes. Combined, these results suggest that zonulin upregulation is associated with increased intestinal permeability in a subgroup of type 1 diabetic patients. Zonulin upregulation seems to precede the onset of the disease, providing a possible link between increased intestinal permeability, environmental exposure to non-self antigens, and the development of autoimmunity in genetically susceptible individuals.

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Year:  2006        PMID: 16644703     DOI: 10.2337/db05-1593

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  184 in total

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9.  Gut barrier disruption by an enteric bacterial pathogen accelerates insulitis in NOD mice.

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