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The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease

BACKGROUND/AIMS: The exact relationship between vitamin D deficiency and inflammatory bowel disease (IBD) remains unclear. We evaluated the effect of vitamin D(3) administration on inflammatory responses and disease severity in patients with IBD. METHODS: We investigated the serum 25-hydroxyvitamin...

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Autores principales: Jun, Jae Chang, Yoon, Hyuk, Choi, Yoon Jin, Shin, Cheol Min, Park, Young Soo, Kim, Nayoung, Lee, Dong Ho, Kim, Joo Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for the Study of Intestinal Diseases 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505089/
https://www.ncbi.nlm.nih.gov/pubmed/30477283
http://dx.doi.org/10.5217/ir.2018.00081
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author Jun, Jae Chang
Yoon, Hyuk
Choi, Yoon Jin
Shin, Cheol Min
Park, Young Soo
Kim, Nayoung
Lee, Dong Ho
Kim, Joo Sung
author_facet Jun, Jae Chang
Yoon, Hyuk
Choi, Yoon Jin
Shin, Cheol Min
Park, Young Soo
Kim, Nayoung
Lee, Dong Ho
Kim, Joo Sung
author_sort Jun, Jae Chang
collection PubMed
description BACKGROUND/AIMS: The exact relationship between vitamin D deficiency and inflammatory bowel disease (IBD) remains unclear. We evaluated the effect of vitamin D(3) administration on inflammatory responses and disease severity in patients with IBD. METHODS: We investigated the serum 25-hydroxyvitamin D(3) [25-(OH)D], C-reactive protein (CRP) levels and the partial Mayo score (PMS) in patients with IBD. Vitamin D(3) was administered in patients with either vitamin D deficiency or insufficiency and CRP, serum vitamin D levels and PMS were re-examined at 6 months of administration. RESULTS: In 88 patients with Crohn’s disease (CD), a negative correlation was found between serum vitamin D and CRP. In 178 patients with ulcerative colitis (UC), serum vitamin D showed no association with CRP or PMS. Serum vitamin D increased from 11.08±3.63 to 22.69±6.11 ng/mL in 29 patients with CD and from 11.45±4.10 to 24.20±6.61 ng/mL in 41 patients with UC who received vitamin D(3) treatment (P<0.001 and P<0.001, respectively). In patients with CD, median ΔCRP was –0.24 in the normalized vitamin D group and –0.11 in the non-normalized group (P=0.308). In patients with UC, median ΔCRP was −0.01 in the normalized vitamin D group and 0.06 in the non-normalized group (P=0.359). CONCLUSIONS: Although a negative correlation was found between serum vitamin D and CRP levels in patients with CD, administration of vitamin D did not improve the CRP level in patients with CD. In patients with UC, serum vitamin D level was unrelated to CRP or PMS.
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spelling pubmed-65050892019-05-20 The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease Jun, Jae Chang Yoon, Hyuk Choi, Yoon Jin Shin, Cheol Min Park, Young Soo Kim, Nayoung Lee, Dong Ho Kim, Joo Sung Intest Res Original Article BACKGROUND/AIMS: The exact relationship between vitamin D deficiency and inflammatory bowel disease (IBD) remains unclear. We evaluated the effect of vitamin D(3) administration on inflammatory responses and disease severity in patients with IBD. METHODS: We investigated the serum 25-hydroxyvitamin D(3) [25-(OH)D], C-reactive protein (CRP) levels and the partial Mayo score (PMS) in patients with IBD. Vitamin D(3) was administered in patients with either vitamin D deficiency or insufficiency and CRP, serum vitamin D levels and PMS were re-examined at 6 months of administration. RESULTS: In 88 patients with Crohn’s disease (CD), a negative correlation was found between serum vitamin D and CRP. In 178 patients with ulcerative colitis (UC), serum vitamin D showed no association with CRP or PMS. Serum vitamin D increased from 11.08±3.63 to 22.69±6.11 ng/mL in 29 patients with CD and from 11.45±4.10 to 24.20±6.61 ng/mL in 41 patients with UC who received vitamin D(3) treatment (P<0.001 and P<0.001, respectively). In patients with CD, median ΔCRP was –0.24 in the normalized vitamin D group and –0.11 in the non-normalized group (P=0.308). In patients with UC, median ΔCRP was −0.01 in the normalized vitamin D group and 0.06 in the non-normalized group (P=0.359). CONCLUSIONS: Although a negative correlation was found between serum vitamin D and CRP levels in patients with CD, administration of vitamin D did not improve the CRP level in patients with CD. In patients with UC, serum vitamin D level was unrelated to CRP or PMS. Korean Association for the Study of Intestinal Diseases 2019-04 2018-11-27 /pmc/articles/PMC6505089/ /pubmed/30477283 http://dx.doi.org/10.5217/ir.2018.00081 Text en © Copyright 2019. Korean Association for the Study of Intestinal Diseases. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jun, Jae Chang
Yoon, Hyuk
Choi, Yoon Jin
Shin, Cheol Min
Park, Young Soo
Kim, Nayoung
Lee, Dong Ho
Kim, Joo Sung
The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease
title The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease
title_full The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease
title_fullStr The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease
title_full_unstemmed The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease
title_short The effect of vitamin D administration on inflammatory markers in patients with inflammatory bowel disease
title_sort effect of vitamin d administration on inflammatory markers in patients with inflammatory bowel disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505089/
https://www.ncbi.nlm.nih.gov/pubmed/30477283
http://dx.doi.org/10.5217/ir.2018.00081
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