Evidence for a Cystic Fibrosis Enteropathy

Previous studies have suggested the existence of enteropathy in cystic fibrosis (CF), which may contribute to intestinal function impairment, a poor nutritional status and decline in lung function. This study evaluated enterocyte damage and intestinal inflammation in CF and studied its associations...

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Veröffentlicht in:PloS one 2015-10, Vol.10 (10), p.e0138062
Hauptverfasser: Adriaanse, Marlou P M, van der Sande, Linda J T M, van den Neucker, Anita M, Menheere, Paul P C A, Dompeling, Edward, Buurman, Wim A, Vreugdenhil, Anita C E
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Sprache:eng
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Zusammenfassung:Previous studies have suggested the existence of enteropathy in cystic fibrosis (CF), which may contribute to intestinal function impairment, a poor nutritional status and decline in lung function. This study evaluated enterocyte damage and intestinal inflammation in CF and studied its associations with nutritional status, CF-related morbidities such as impaired lung function and diabetes, and medication use. Sixty-eight CF patients and 107 controls were studied. Levels of serum intestinal-fatty acid binding protein (I-FABP), a specific marker for enterocyte damage, were retrospectively determined. The faecal intestinal inflammation marker calprotectin was prospectively studied. Nutritional status, lung function (FEV1), exocrine pancreatic insufficiency (EPI), CF-related diabetes (CFRD) and use of proton pump inhibitors (PPI) were obtained from the medical charts. Serum I-FABP levels were elevated in CF patients as compared with controls (p
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0138062