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Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects

The association between gut microbiota and circulating zonulin level, a marker of intestinal permeability, has not been studied yet. The aim of the study is the assessment of plasma zonulin, haptoglobin and proinflammatory cytokines (TNF-α and IL-6) levels in relation to composition of gut microbiot...

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Autores principales: Żak-Gołąb, Agnieszka, Kocełak, Piotr, Aptekorz, Małgorzata, Zientara, Maria, Juszczyk, Łukasz, Martirosian, Gayane, Chudek, Jerzy, Olszanecka-Glinianowicz, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732644/
https://www.ncbi.nlm.nih.gov/pubmed/23970898
http://dx.doi.org/10.1155/2013/674106
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author Żak-Gołąb, Agnieszka
Kocełak, Piotr
Aptekorz, Małgorzata
Zientara, Maria
Juszczyk, Łukasz
Martirosian, Gayane
Chudek, Jerzy
Olszanecka-Glinianowicz, Magdalena
author_facet Żak-Gołąb, Agnieszka
Kocełak, Piotr
Aptekorz, Małgorzata
Zientara, Maria
Juszczyk, Łukasz
Martirosian, Gayane
Chudek, Jerzy
Olszanecka-Glinianowicz, Magdalena
author_sort Żak-Gołąb, Agnieszka
collection PubMed
description The association between gut microbiota and circulating zonulin level, a marker of intestinal permeability, has not been studied yet. The aim of the study is the assessment of plasma zonulin, haptoglobin and proinflammatory cytokines (TNF-α and IL-6) levels in relation to composition of gut microbiota in obese and normal weight subjects. Circulating inflammation markers, such as TNF-α, sTNFR1, sTNFR2, IL-6, zonulin, and haptoglobin levels were measured and semiquantitative analysis of gut microbiota composition was carried out in 50 obese and 30 normal weight subjects without concomitant diseases. Higher circulating zonulin, TNF-α, sTNFR1, sTNFR2, and IL-6 levels were found in the obese subjects. Plasma zonulin level correlated positively with age (r = 0.43, P < 0.001), body mass (r = 0.30, P < 0.01), BMI (r = 0.33, P < 0.01), fat mass and fat percentage (r = 0.31, P < 0.01 and r = 0.23, P < 0.05, resp.). Positive correlations between bacterial colony count and sTNFR1 (r = 0.33, P < 0.01) and plasma zonulin (r = 0.26, P < 0.05) but not haptoglobin levels were found. Additionally, plasma zonulin level was proportional to daily energy intake (r = 0.27, P < 0.05) and serum glucose concentration (r = 0.18, P < 0.05) and inversely proportional to diet protein percentage (r = −0.23, P < 0.05). Gut microbiota-related systemic microinflammation in the obese is reflected by circulating zonulin level, a potential marker of interstitial permeability.
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spelling pubmed-37326442013-08-22 Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects Żak-Gołąb, Agnieszka Kocełak, Piotr Aptekorz, Małgorzata Zientara, Maria Juszczyk, Łukasz Martirosian, Gayane Chudek, Jerzy Olszanecka-Glinianowicz, Magdalena Int J Endocrinol Research Article The association between gut microbiota and circulating zonulin level, a marker of intestinal permeability, has not been studied yet. The aim of the study is the assessment of plasma zonulin, haptoglobin and proinflammatory cytokines (TNF-α and IL-6) levels in relation to composition of gut microbiota in obese and normal weight subjects. Circulating inflammation markers, such as TNF-α, sTNFR1, sTNFR2, IL-6, zonulin, and haptoglobin levels were measured and semiquantitative analysis of gut microbiota composition was carried out in 50 obese and 30 normal weight subjects without concomitant diseases. Higher circulating zonulin, TNF-α, sTNFR1, sTNFR2, and IL-6 levels were found in the obese subjects. Plasma zonulin level correlated positively with age (r = 0.43, P < 0.001), body mass (r = 0.30, P < 0.01), BMI (r = 0.33, P < 0.01), fat mass and fat percentage (r = 0.31, P < 0.01 and r = 0.23, P < 0.05, resp.). Positive correlations between bacterial colony count and sTNFR1 (r = 0.33, P < 0.01) and plasma zonulin (r = 0.26, P < 0.05) but not haptoglobin levels were found. Additionally, plasma zonulin level was proportional to daily energy intake (r = 0.27, P < 0.05) and serum glucose concentration (r = 0.18, P < 0.05) and inversely proportional to diet protein percentage (r = −0.23, P < 0.05). Gut microbiota-related systemic microinflammation in the obese is reflected by circulating zonulin level, a potential marker of interstitial permeability. Hindawi Publishing Corporation 2013 2013-07-18 /pmc/articles/PMC3732644/ /pubmed/23970898 http://dx.doi.org/10.1155/2013/674106 Text en Copyright © 2013 Agnieszka Żak-Gołąb et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Żak-Gołąb, Agnieszka
Kocełak, Piotr
Aptekorz, Małgorzata
Zientara, Maria
Juszczyk, Łukasz
Martirosian, Gayane
Chudek, Jerzy
Olszanecka-Glinianowicz, Magdalena
Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects
title Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects
title_full Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects
title_fullStr Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects
title_full_unstemmed Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects
title_short Gut Microbiota, Microinflammation, Metabolic Profile, and Zonulin Concentration in Obese and Normal Weight Subjects
title_sort gut microbiota, microinflammation, metabolic profile, and zonulin concentration in obese and normal weight subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732644/
https://www.ncbi.nlm.nih.gov/pubmed/23970898
http://dx.doi.org/10.1155/2013/674106
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