Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission

Background: Vitamin D deficiency is associated with active Crohn’s disease (CD). However, it remains unclear if lower 25-hydroxyvitamin D [25(OH)D] concentration is the cause, or consequence, of intestinal inflammation. Existing literature has focused on circulating 25(OH)D rather than the active me...

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Main Authors: Craig Haifer, Ian C. Lawrance, Jacqueline R. Center, Michael W. Clarke, Prue H. Hart, John A. Eisman, Robyn Lucas, Simon Ghaly
Format: Article
Language:English
Published: SAGE Publishing 2019-07-01
Series:Therapeutic Advances in Gastroenterology
Online Access:https://doi.org/10.1177/1756284819865144
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spelling doaj-86308fa9220a4d4cb73728138e49cfbc2020-11-25T03:46:03ZengSAGE PublishingTherapeutic Advances in Gastroenterology1756-28482019-07-011210.1177/1756284819865144Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remissionCraig HaiferIan C. LawranceJacqueline R. CenterMichael W. ClarkePrue H. HartJohn A. EismanRobyn LucasSimon GhalyBackground: Vitamin D deficiency is associated with active Crohn’s disease (CD). However, it remains unclear if lower 25-hydroxyvitamin D [25(OH)D] concentration is the cause, or consequence, of intestinal inflammation. Existing literature has focused on circulating 25(OH)D rather than the active metabolite 1,25(OH) 2 D, or its breakdown product, 24,25(OH) 2 D. We aimed to characterise vitamin D metabolism in a cohort of patients with active and inactive CD. Methods: Fifty-four patients with CD and not on corticosteroids or vitamin D supplements, were enrolled in a 6-month prospective cohort study. Sera were collected on enrolment and at 6 months and tested for 25(OH)D, 1,25(OH) 2 D, 24,25(OH) 2 D using liquid chromatography tandem mass spectroscopy as well as vitamin-D-binding protein. Results: There were no differences in 25(OH)D or 1,25(OH) 2 D levels between participants with active versus inactive disease. Levels of 24,25(OH) 2 D were significantly lower in those with active compared with inactive disease (mean 3.9 versus 6.0 µmol/l; p  = 0.007) and therefore the ratio of 25(OH)D:24,25(OH) 2 D was higher (mean 17.3 versus 11.1; p  = 0.001). In those patients with active disease who achieved remission, there was a mean increase in 25(OH)D of 32.3 nmol/l (i.e. to a level in the sufficient range) and 24,25(OH) 2 D of 2.1 µmol/l. These increases were not seen in patients with persistently active or inactive disease. Conclusion: Levels of 24,25(OH) 2 D, but not 25(OH)D, were lower in patients with active CD, and spontaneously increased with resolution of underlying inflammation. The utility of 24,25(OH) 2 D as a biomarker of disease activity and vitamin D status in CD warrants further exploration.https://doi.org/10.1177/1756284819865144
collection DOAJ
language English
format Article
sources DOAJ
author Craig Haifer
Ian C. Lawrance
Jacqueline R. Center
Michael W. Clarke
Prue H. Hart
John A. Eisman
Robyn Lucas
Simon Ghaly
spellingShingle Craig Haifer
Ian C. Lawrance
Jacqueline R. Center
Michael W. Clarke
Prue H. Hart
John A. Eisman
Robyn Lucas
Simon Ghaly
Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission
Therapeutic Advances in Gastroenterology
author_facet Craig Haifer
Ian C. Lawrance
Jacqueline R. Center
Michael W. Clarke
Prue H. Hart
John A. Eisman
Robyn Lucas
Simon Ghaly
author_sort Craig Haifer
title Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission
title_short Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission
title_full Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission
title_fullStr Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission
title_full_unstemmed Vitamin D metabolites are lower with active Crohn’s disease and spontaneously recover with development of remission
title_sort vitamin d metabolites are lower with active crohn’s disease and spontaneously recover with development of remission
publisher SAGE Publishing
series Therapeutic Advances in Gastroenterology
issn 1756-2848
publishDate 2019-07-01
description Background: Vitamin D deficiency is associated with active Crohn’s disease (CD). However, it remains unclear if lower 25-hydroxyvitamin D [25(OH)D] concentration is the cause, or consequence, of intestinal inflammation. Existing literature has focused on circulating 25(OH)D rather than the active metabolite 1,25(OH) 2 D, or its breakdown product, 24,25(OH) 2 D. We aimed to characterise vitamin D metabolism in a cohort of patients with active and inactive CD. Methods: Fifty-four patients with CD and not on corticosteroids or vitamin D supplements, were enrolled in a 6-month prospective cohort study. Sera were collected on enrolment and at 6 months and tested for 25(OH)D, 1,25(OH) 2 D, 24,25(OH) 2 D using liquid chromatography tandem mass spectroscopy as well as vitamin-D-binding protein. Results: There were no differences in 25(OH)D or 1,25(OH) 2 D levels between participants with active versus inactive disease. Levels of 24,25(OH) 2 D were significantly lower in those with active compared with inactive disease (mean 3.9 versus 6.0 µmol/l; p  = 0.007) and therefore the ratio of 25(OH)D:24,25(OH) 2 D was higher (mean 17.3 versus 11.1; p  = 0.001). In those patients with active disease who achieved remission, there was a mean increase in 25(OH)D of 32.3 nmol/l (i.e. to a level in the sufficient range) and 24,25(OH) 2 D of 2.1 µmol/l. These increases were not seen in patients with persistently active or inactive disease. Conclusion: Levels of 24,25(OH) 2 D, but not 25(OH)D, were lower in patients with active CD, and spontaneously increased with resolution of underlying inflammation. The utility of 24,25(OH) 2 D as a biomarker of disease activity and vitamin D status in CD warrants further exploration.
url https://doi.org/10.1177/1756284819865144
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