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Serum adropin levels are reduced in patients with inflammatory bowel diseases

Adropin is a novel peptide mostly associated with energy homeostasis and vascular protection. To our knowledge, there are no studies that investigated its relationship with inflammatory bowel diseases (IBD). The aim of this study was to compare serum adropin levels between 55 patients with IBD (30 U...

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Autores principales: Brnić, Darko, Martinovic, Dinko, Zivkovic, Piero Marin, Tokic, Daria, Tadin Hadjina, Ivana, Rusic, Doris, Vilovic, Marino, Supe-Domic, Daniela, Tonkic, Ante, Bozic, Josko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283308/
https://www.ncbi.nlm.nih.gov/pubmed/32518265
http://dx.doi.org/10.1038/s41598-020-66254-9
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author Brnić, Darko
Martinovic, Dinko
Zivkovic, Piero Marin
Tokic, Daria
Tadin Hadjina, Ivana
Rusic, Doris
Vilovic, Marino
Supe-Domic, Daniela
Tonkic, Ante
Bozic, Josko
author_facet Brnić, Darko
Martinovic, Dinko
Zivkovic, Piero Marin
Tokic, Daria
Tadin Hadjina, Ivana
Rusic, Doris
Vilovic, Marino
Supe-Domic, Daniela
Tonkic, Ante
Bozic, Josko
author_sort Brnić, Darko
collection PubMed
description Adropin is a novel peptide mostly associated with energy homeostasis and vascular protection. To our knowledge, there are no studies that investigated its relationship with inflammatory bowel diseases (IBD). The aim of this study was to compare serum adropin levels between 55 patients with IBD (30 Ulcerative colitis (UC) patients, 25 Crohn’s disease (CD) patients) and 50 age/gender matched controls. Furthermore, we explored adropin correlations with IBD severity scores, hsCRP, fecal calprotectin, fasting glucose and insulin levels. Serum adropin levels were significantly lower in patients with IBD in comparison with the control group (2.89 ± 0.94 vs 3.37 ± 0.60 ng/mL, P = 0.002), while there was no significant difference in comparison of UC patients with CD patients (P = 0.585). Furthermore, there was a negative correlation between adropin and fecal calprotectin (r = −0.303, P = 0.025), whereas in the total study population, we found a significant negative correlation with fasting glucose levels (r = −0.222, P = 0.023). A multivariable logistic regression showed that serum adropin was a significant predictor of positive IBD status when enumerated along with baseline characteristics (OR 0.455, 95% CI 0.251–0.823, P = 0.009). Our findings imply that adropin could be involved in complex pathophysiology of IBD, but further larger scale studies are needed to address these findings.
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spelling pubmed-72833082020-06-15 Serum adropin levels are reduced in patients with inflammatory bowel diseases Brnić, Darko Martinovic, Dinko Zivkovic, Piero Marin Tokic, Daria Tadin Hadjina, Ivana Rusic, Doris Vilovic, Marino Supe-Domic, Daniela Tonkic, Ante Bozic, Josko Sci Rep Article Adropin is a novel peptide mostly associated with energy homeostasis and vascular protection. To our knowledge, there are no studies that investigated its relationship with inflammatory bowel diseases (IBD). The aim of this study was to compare serum adropin levels between 55 patients with IBD (30 Ulcerative colitis (UC) patients, 25 Crohn’s disease (CD) patients) and 50 age/gender matched controls. Furthermore, we explored adropin correlations with IBD severity scores, hsCRP, fecal calprotectin, fasting glucose and insulin levels. Serum adropin levels were significantly lower in patients with IBD in comparison with the control group (2.89 ± 0.94 vs 3.37 ± 0.60 ng/mL, P = 0.002), while there was no significant difference in comparison of UC patients with CD patients (P = 0.585). Furthermore, there was a negative correlation between adropin and fecal calprotectin (r = −0.303, P = 0.025), whereas in the total study population, we found a significant negative correlation with fasting glucose levels (r = −0.222, P = 0.023). A multivariable logistic regression showed that serum adropin was a significant predictor of positive IBD status when enumerated along with baseline characteristics (OR 0.455, 95% CI 0.251–0.823, P = 0.009). Our findings imply that adropin could be involved in complex pathophysiology of IBD, but further larger scale studies are needed to address these findings. Nature Publishing Group UK 2020-06-09 /pmc/articles/PMC7283308/ /pubmed/32518265 http://dx.doi.org/10.1038/s41598-020-66254-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Brnić, Darko
Martinovic, Dinko
Zivkovic, Piero Marin
Tokic, Daria
Tadin Hadjina, Ivana
Rusic, Doris
Vilovic, Marino
Supe-Domic, Daniela
Tonkic, Ante
Bozic, Josko
Serum adropin levels are reduced in patients with inflammatory bowel diseases
title Serum adropin levels are reduced in patients with inflammatory bowel diseases
title_full Serum adropin levels are reduced in patients with inflammatory bowel diseases
title_fullStr Serum adropin levels are reduced in patients with inflammatory bowel diseases
title_full_unstemmed Serum adropin levels are reduced in patients with inflammatory bowel diseases
title_short Serum adropin levels are reduced in patients with inflammatory bowel diseases
title_sort serum adropin levels are reduced in patients with inflammatory bowel diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283308/
https://www.ncbi.nlm.nih.gov/pubmed/32518265
http://dx.doi.org/10.1038/s41598-020-66254-9
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