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Increased plasma zonulin in patients with sepsis
INTRODUCTION: Zonulin is a eukaryotic protein structurally similar to Vibrio cholerae’s zonula occludens toxin. It plays an important role in the opening of small intestine tight junctions. The loss of gut wall integrity during sepsis might be pivotal and has been described in various experimental a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Croatian Society of Medical Biochemistry and Laboratory Medicine
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900088/ https://www.ncbi.nlm.nih.gov/pubmed/23457771 http://dx.doi.org/10.11613/BM.2013.013 |
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author | Klaus, Daniel A. Motal, Michael C. Burger-Klepp, Ursula Marschalek, Corinna Schmidt, Elisabeth M. Lebherz-Eichinger, Diana Krenn, Claus G. Roth, Georg A. |
author_facet | Klaus, Daniel A. Motal, Michael C. Burger-Klepp, Ursula Marschalek, Corinna Schmidt, Elisabeth M. Lebherz-Eichinger, Diana Krenn, Claus G. Roth, Georg A. |
author_sort | Klaus, Daniel A. |
collection | PubMed |
description | INTRODUCTION: Zonulin is a eukaryotic protein structurally similar to Vibrio cholerae’s zonula occludens toxin. It plays an important role in the opening of small intestine tight junctions. The loss of gut wall integrity during sepsis might be pivotal and has been described in various experimental as well as human studies. Increased levels of zonulin could be demonstrated in diseases associated with increased intestinal inflammation, such as celiac disease and type 1 diabetes. We therefore investigated the role of plasma levels of zonulin in patients with sepsis as a non-invasive marker of gut wall integrity. MATERIALS AND METHODS: Plasma level of zonulin was measured in 25 patients with sepsis, severe sepsis or septic shock according to ACCP/SCCM criteria at the first day of diagnosed sepsis. 18 non-septic post-surgical ICU-patients and 20 healthy volunteers served as control. Plasma levels were determined by using commercially available ELISA kit. Data are given as median and interquartile range (IQR). RESULTS: Significantly higher plasma concentration of zonulin were found in the sepsis group: 6.61 ng/mL (IQR 3.51–9.46), as compared to the to the post-surgical control group: 3.40 ng/mL (IQR 2.14–5.70) (P = 0.025), as well as to the healthy group: 3.55 ng/mL (IQR 3.14–4.14) (P = 0.008). CONCLUSION: We were able demonstrate elevated levels of plasma zonulin, a potential marker of intestinal permeability in septic patients. Increased zonulin may serve as an additional mechanism for the observed increased intestinal permeability during sepsis and SIRS. |
format | Online Article Text |
id | pubmed-3900088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Croatian Society of Medical Biochemistry and Laboratory Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-39000882014-01-23 Increased plasma zonulin in patients with sepsis Klaus, Daniel A. Motal, Michael C. Burger-Klepp, Ursula Marschalek, Corinna Schmidt, Elisabeth M. Lebherz-Eichinger, Diana Krenn, Claus G. Roth, Georg A. Biochem Med (Zagreb) Original Paper INTRODUCTION: Zonulin is a eukaryotic protein structurally similar to Vibrio cholerae’s zonula occludens toxin. It plays an important role in the opening of small intestine tight junctions. The loss of gut wall integrity during sepsis might be pivotal and has been described in various experimental as well as human studies. Increased levels of zonulin could be demonstrated in diseases associated with increased intestinal inflammation, such as celiac disease and type 1 diabetes. We therefore investigated the role of plasma levels of zonulin in patients with sepsis as a non-invasive marker of gut wall integrity. MATERIALS AND METHODS: Plasma level of zonulin was measured in 25 patients with sepsis, severe sepsis or septic shock according to ACCP/SCCM criteria at the first day of diagnosed sepsis. 18 non-septic post-surgical ICU-patients and 20 healthy volunteers served as control. Plasma levels were determined by using commercially available ELISA kit. Data are given as median and interquartile range (IQR). RESULTS: Significantly higher plasma concentration of zonulin were found in the sepsis group: 6.61 ng/mL (IQR 3.51–9.46), as compared to the to the post-surgical control group: 3.40 ng/mL (IQR 2.14–5.70) (P = 0.025), as well as to the healthy group: 3.55 ng/mL (IQR 3.14–4.14) (P = 0.008). CONCLUSION: We were able demonstrate elevated levels of plasma zonulin, a potential marker of intestinal permeability in septic patients. Increased zonulin may serve as an additional mechanism for the observed increased intestinal permeability during sepsis and SIRS. Croatian Society of Medical Biochemistry and Laboratory Medicine 2013-02-15 /pmc/articles/PMC3900088/ /pubmed/23457771 http://dx.doi.org/10.11613/BM.2013.013 Text en ©Copyright by Croatian Society of Medical Biochemistry and Laboratory Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Klaus, Daniel A. Motal, Michael C. Burger-Klepp, Ursula Marschalek, Corinna Schmidt, Elisabeth M. Lebherz-Eichinger, Diana Krenn, Claus G. Roth, Georg A. Increased plasma zonulin in patients with sepsis |
title | Increased plasma zonulin in patients with sepsis |
title_full | Increased plasma zonulin in patients with sepsis |
title_fullStr | Increased plasma zonulin in patients with sepsis |
title_full_unstemmed | Increased plasma zonulin in patients with sepsis |
title_short | Increased plasma zonulin in patients with sepsis |
title_sort | increased plasma zonulin in patients with sepsis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900088/ https://www.ncbi.nlm.nih.gov/pubmed/23457771 http://dx.doi.org/10.11613/BM.2013.013 |
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