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

被引:413
作者
Sapone, A
de Magistris, L
Pietzak, M
Clemente, MG
Tripathi, A
Cucca, F
Lampis, R
Kryszak, D
Cartenì, M
Generoso, M
Iafusco, D
Prisco, F
Laghi, F
Riegler, G
Carratu, R
Counts, D
Fasano, A
机构
[1] Univ Maryland, Sch Med, Mucosl Biol Res Ctr, Baltimore, MD 21201 USA
[2] II Univ Naples, Gastroenterol Unit, Dept Magrassi Lanzara, Naples, Italy
[3] Univ So Calif, Keck Sch Med, Los Angeles, CA USA
[4] Childrens Hosp Los Angeles, Div Gastroenterol & Nutr, Los Angeles, CA 90027 USA
[5] Univ Cagliari, Dept Biomed Sci & Biotechnol, Cagliari, Italy
[6] Univ Maryland, Sch Med, Dept Pediat, Div Pediat Endocrinol, Baltimore, MD 21201 USA
关键词
D O I
10.2337/db05-1593
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1443 / 1449
页数:7
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