Increased vitamin D binding protein levels are associated with irritable bowel syndrome

dc.contributor.authorElif BÖREKÇİ
dc.contributor.authorMahmut KILIÇ
dc.contributor.authorZeynep OZAN
dc.contributor.authorHasan BÖREKÇİ
dc.contributor.authorTekin YILDIRIM
dc.contributor.authorYeşim GÖÇMEN
dc.contributor.authorHatice BAŞ
dc.date.accessioned2024-07-24T09:10:39Z
dc.date.available2024-07-24T09:10:39Z
dc.date.issued2021
dc.description.abstractidentify Irritable bowel syndrome (IBS) and its subtypes. The aim of this study is to explore potential serum biomarkers that may be associated with IBS subtypes, particularly in the vitamin D pathway. Methods: The study population comprised 75 IBS patients and 79 controls. Patients divided into IBS subtypes. Routine biochemical parameters, 25-OH-vitamin D, vitamin D binding protein (VDBP) and vitamin D receptor (VDR) serum levels were compared between IBS subtypes and controls. Factors related to IBS subtypes were examined by multivariate logistic regression analysis. Results: Vitamin D levels were lower; VDBP and VDR were higher in all IBS patients than in controls (p<0.001; 0.047 and 0.029, respectively). According to logistic regression analysis, VDBP was a disease-related parameter as much as vitamin D in all IBS subtypes. C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) were higher especially in diarrhea-dominant IBS (IBS-D) (p=0.041; 0.046) and vitamin B12 were significantly lower in constipation-dominant IBS (IBS-C) (p=0.001). Conclusions: Increased VDBP levels were associated with all IBS subtypes. Patients, especially in IBS-D, had higher serum levels of VDBP, CRP and ESR. Vitamin B12 deficiency, which we consider as a result of the disease, was more common in IBS-C.
dc.identifier.DOI-ID10.1515/tjb-2020-0305
dc.identifier.issn1303-829X
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/23094
dc.language.isoeng
dc.titleIncreased vitamin D binding protein levels are associated with irritable bowel syndrome
dc.typeAraştırma Makalesi

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