Increased intestinal permeability in patients with short bowel syndrome is not affected by parenteral nutrition
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
31424246
DOI
10.33549/physiolres.934134
PII: 934134
Knihovny.cz E-resources
- MeSH
- Biomarkers blood MeSH
- Citrulline blood MeSH
- Glucagon-Like Peptide 2 blood MeSH
- Haptoglobins MeSH
- Intestinal Absorption * MeSH
- Middle Aged MeSH
- Humans MeSH
- Membrane Glycoproteins blood MeSH
- Parenteral Nutrition * MeSH
- Permeability MeSH
- Protein Precursors blood MeSH
- Acute-Phase Proteins MeSH
- Fatty Acid-Binding Proteins blood MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Short Bowel Syndrome blood diagnosis physiopathology therapy MeSH
- Intestine, Small metabolism physiopathology MeSH
- Carrier Proteins blood MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- Citrulline MeSH
- FABP2 protein, human MeSH Browser
- Glucagon-Like Peptide 2 MeSH
- Haptoglobins MeSH
- lipopolysaccharide-binding protein MeSH Browser
- Membrane Glycoproteins MeSH
- Protein Precursors MeSH
- Acute-Phase Proteins MeSH
- Fatty Acid-Binding Proteins MeSH
- Carrier Proteins MeSH
- zonulin MeSH Browser
The aim of our study was to assess the presence and degree of intestinal leakage in subjects suffering from short bowel syndrome (SBS) and its modification by parenteral nutrition. To this end we assessed circulating levels of selected makers of intestinal permeability including zonulin, fatty acid binding protein 2 (FABP-2), citrulline and glucagon-like peptide 2 (GLP-2). We also measured lipopolysaccharide binding protein (LBP) as a marker of circulating levels of lipopolysaccharide acting through the CD14 molecule. Eleven SBS and 10 age- and BMI-matched control subjects were included into the study. The effect of parenteral nutrition was assessed after 14 days, 6 and 12 months from its initiation, respectively. At baseline, SBS patients had increased gut permeability as measured by zonulin (47.24+/-2.14 vs. 39.48+/-1.20 ng/ml, p=0.006) and LBP (30.32+/-13.25 vs. 9.77+/-0.71 microg/ml, p<0.001) compared to healthy controls. Furthermore, SBS subjects had reduced FABP-2, unchanged citrulline and increased sCD14 and GLP-2 relative to control group. Throughout the whole study period the administered parenteral nutrition had no significant effect on any of the studied parameters. Taken together, our data show that patients with short bowel syndrome have increased intestinal permeability that is not affected by parenteral nutrition.
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