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Association of selected adipokines with vitamin D deficiency in children with inflammatory bowel disease
M. Geryk, V. Kucerova, M. Velganova-Veghova, H. Foltenova, K. Bouchalova, D. Karasek, M. Radvansky, E. Karaskova
Language English Country England, Great Britain
Document type Journal Article
Grant support
IGA LF 2023_037
Palacky University Olomouc
IGA LF 2024_040
Palacky University Olomouc
IGA LF 2024_040
Palacky University Olomouc
MH CZ DRO (FNOl, 00098892)
Ministerstvo Zdravotnictví Ceské Republiky
MH CZ DRO (FNOl, 00098892)
Ministerstvo Zdravotnictví Ceské Republiky
MH CZ DRO (FNOl, 00098892)
Ministerstvo Zdravotnictví Ceské Republiky
NLK
BioMedCentral
from 2001-12-01
BioMedCentral Open Access
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Directory of Open Access Journals
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Free Medical Journals
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PubMed Central
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Europe PubMed Central
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ProQuest Central
from 2009-01-01
Open Access Digital Library
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Open Access Digital Library
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Open Access Digital Library
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Medline Complete (EBSCOhost)
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Health & Medicine (ProQuest)
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ROAD: Directory of Open Access Scholarly Resources
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Springer Nature OA/Free Journals
from 2001-12-01
- MeSH
- Adipokines * blood MeSH
- Adiponectin blood deficiency MeSH
- Biomarkers blood MeSH
- Child MeSH
- DNA-Binding Proteins blood MeSH
- Inflammatory Bowel Diseases blood complications MeSH
- Humans MeSH
- Adolescent MeSH
- Vitamin D Deficiency * complications blood MeSH
- Nucleobindins blood MeSH
- Retinol-Binding Proteins, Plasma metabolism analysis MeSH
- Fatty Acid-Binding Proteins blood MeSH
- Calcium-Binding Proteins blood MeSH
- Resistin blood MeSH
- Case-Control Studies MeSH
- Vitamin D * blood analogs & derivatives MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: Adipose tissue is significantly involved in inflammatory bowel disease (IBD). Vitamin D can affect both adipogenesis and inflammation. The aim of this study was to compare the production of selected adipokines, potentially involved in the pathogenesis of IBD - adiponectin, resistin, retinol binding protein 4 (RBP-4), adipocyte fatty acid binding protein and nesfatin-1 in children with IBD according to the presence of 25-hydroxyvitamin D (25(OH)D) deficiency. METHODS: The study was conducted as a case-control study in pediatric patients with IBD and healthy children of the same sex and age. In addition to adipokines and 25(OH)D, anthropometric parameters, markers of inflammation and disease activity were assessed in all participants. RESULTS: Children with IBD had significantly higher resistin levels regardless of 25(OH)D levels. IBD patients with 25(OH)D deficiency only had significantly lower RBP-4 compared to healthy controls and also compared to IBD patients without 25(OH)D deficiency. No other significant differences in adipokines were found in children with IBD with or without 25(OH)D deficiency. 25(OH)D levels in IBD patients corelated with RBP-4 only, and did not correlate with other adipokines. CONCLUSIONS: Whether the lower RBP-4 levels in the 25(OH)D-deficient group of IBD patients directly reflect vitamin D deficiency remains uncertain. The production of other adipokines does not appear to be directly related to vitamin D deficiency.
References provided by Crossref.org
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- $a BACKGROUND: Adipose tissue is significantly involved in inflammatory bowel disease (IBD). Vitamin D can affect both adipogenesis and inflammation. The aim of this study was to compare the production of selected adipokines, potentially involved in the pathogenesis of IBD - adiponectin, resistin, retinol binding protein 4 (RBP-4), adipocyte fatty acid binding protein and nesfatin-1 in children with IBD according to the presence of 25-hydroxyvitamin D (25(OH)D) deficiency. METHODS: The study was conducted as a case-control study in pediatric patients with IBD and healthy children of the same sex and age. In addition to adipokines and 25(OH)D, anthropometric parameters, markers of inflammation and disease activity were assessed in all participants. RESULTS: Children with IBD had significantly higher resistin levels regardless of 25(OH)D levels. IBD patients with 25(OH)D deficiency only had significantly lower RBP-4 compared to healthy controls and also compared to IBD patients without 25(OH)D deficiency. No other significant differences in adipokines were found in children with IBD with or without 25(OH)D deficiency. 25(OH)D levels in IBD patients corelated with RBP-4 only, and did not correlate with other adipokines. CONCLUSIONS: Whether the lower RBP-4 levels in the 25(OH)D-deficient group of IBD patients directly reflect vitamin D deficiency remains uncertain. The production of other adipokines does not appear to be directly related to vitamin D deficiency.
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