Serum adropin levels are reduced in patients with inflammatory bowel diseases

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作者
Darko Brnić
Dinko Martinovic
Piero Marin Zivkovic
Daria Tokic
Ivana Tadin Hadjina
Doris Rusic
Marino Vilovic
Daniela Supe-Domic
Ante Tonkic
Josko Bozic
机构
[1] Department of Gastroenterology,
[2] University Hospital of Split,undefined
[3] Institute of Emergency Medicine of Split-Dalmatia County,undefined
[4] Department of Pathophysiology,undefined
[5] University of Split School of Medicine,undefined
[6] Department of Pharmacy,undefined
[7] University of Split School of Medicine,undefined
[8] Department of Medical Laboratory Diagnostics,undefined
[9] University Hospital of Split,undefined
[10] Department of Health Studies,undefined
[11] University of Split,undefined
[12] Department of Internal Medicine,undefined
[13] University of Split School of Medicine,undefined
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摘要
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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