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Markers of Intestinal Permeability and Inflammation in Enterally Fed Children with Cerebral Palsy.

Authors :
Mickiewicz-Góra D
Sznurkowska K
Skonieczna-Żydecka K
Drozd A
Borkowska A
Zagierski M
Troch J
Szlagatys-Sidorkiewicz A
Source :
Nutrients [Nutrients] 2024 Jul 27; Vol. 16 (15). Date of Electronic Publication: 2024 Jul 27.
Publication Year :
2024

Abstract

Cerebral palsy (CP) results in non-progressive damage to the central nervous system, leading to functional disorders of the gastrointestinal tract and requiring enteral nutrition via gastrostomy in some patients. The aim of the study was to assess the impact of enteral nutrition on intestinal inflammation expressed by stool calprotectin and intestinal permeability determined by fecal zonulin and IFABP, and to determine whether CP affects these parameters. The study group consisted of 30 children with CP, fed enterally (Cerebral Palsy Enteral Nutrition-CPEN), and two reference groups: 24 children with CP, fed orally with a standard diet (CPC-Cerebral Palsy Controls) and 24 healthy children (HC-healthy controls). The differences between these groups and between the combined CP groups (CPG and CPEN + CPC) and HC were analyzed. Fecal zonulin, calprotectin, and intestinal fatty acid-binding protein 2 (IFABP2) levels were determined by ELISA. The concentrations of fecal calprotectin and zonulin were significantly higher in the CPEN group than in the CPC group ( p = 0.012, p = 0.025). When comparing the CPG ( n = 53) with the HC group ( n = 24), statistically significant differences were observed for calprotectin ( p = 0.000018, higher in the CPG) and IFABP ( p = 0.021, higher in HC). Enteral nutrition was associated in our cohort with increased fecal calprotectin and zonulin. Children with cerebral palsy presented with increased fecal calprotectin but not increased intestinal permeability expressed by stool zonulin.

Details

Language :
English
ISSN :
2072-6643
Volume :
16
Issue :
15
Database :
MEDLINE
Journal :
Nutrients
Publication Type :
Academic Journal
Accession number :
39125328
Full Text :
https://doi.org/10.3390/nu16152447