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The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH

Vitamin D status, assessed by serum concentration of 25(OH)D, is the prime candidate marker for many disease-association studies, but the interplay between the subsequent 1,25-dihydroxyvitamin D (1,25(OH)(2)D) and 24,25-dihydroxyvitamin D (24,25(OH)(2)D) metabolites is unclear. In this study, we con...

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Autores principales: Tang, Jonathan C. Y., Jackson, Sarah, Walsh, Neil P., Greeves, Julie, Fraser, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502854/
https://www.ncbi.nlm.nih.gov/pubmed/31061425
http://dx.doi.org/10.1038/s41598-019-43462-6
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author Tang, Jonathan C. Y.
Jackson, Sarah
Walsh, Neil P.
Greeves, Julie
Fraser, William D.
author_facet Tang, Jonathan C. Y.
Jackson, Sarah
Walsh, Neil P.
Greeves, Julie
Fraser, William D.
author_sort Tang, Jonathan C. Y.
collection PubMed
description Vitamin D status, assessed by serum concentration of 25(OH)D, is the prime candidate marker for many disease-association studies, but the interplay between the subsequent 1,25-dihydroxyvitamin D (1,25(OH)(2)D) and 24,25-dihydroxyvitamin D (24,25(OH)(2)D) metabolites is unclear. In this study, we conducted an analysis from a large cohort of healthy, physically fit, young army recruits (n = 940). We found a significant, inverse relationship between serum 25(OH)D and 1,25(OH)(2)D:24,25(OH)(2)D vitamin D metabolite ratio (VMR) (r(2)Exp = 0.582, p < 0.0001), and demonstrated a significant association with increasing PTH concentration (p < 0.001). Circannual rhythms were evident for all vitamin D metabolites and VMRs except for 1,25(OH)(2)D when fitted to Cosinor curves. We estimated 1,25(OH)(2)D:24,25(OH)(2)D VMR of ≥35 to be the threshold value for vitamin D insufficiency, and ≥51 to be predictive of vitamin D deficiency. Our three-dimensional model provides mechanistic insight into the vitamin D-PTH endocrine system, and further substantiates the role of 24,25(OH)(2)D in human physiology. The model sets a new paradigm for vitamin D treatment strategy, and may help the establishment of vitamin D-adjusted PTH reference intervals. The study was approved by the UK Ministry of Defence research ethics committee (MODREC 165/Gen/10 and 692/MoDREC/15). ClinicalTrials.gov Identifier NCT02416895.
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spelling pubmed-65028542019-05-20 The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH Tang, Jonathan C. Y. Jackson, Sarah Walsh, Neil P. Greeves, Julie Fraser, William D. Sci Rep Article Vitamin D status, assessed by serum concentration of 25(OH)D, is the prime candidate marker for many disease-association studies, but the interplay between the subsequent 1,25-dihydroxyvitamin D (1,25(OH)(2)D) and 24,25-dihydroxyvitamin D (24,25(OH)(2)D) metabolites is unclear. In this study, we conducted an analysis from a large cohort of healthy, physically fit, young army recruits (n = 940). We found a significant, inverse relationship between serum 25(OH)D and 1,25(OH)(2)D:24,25(OH)(2)D vitamin D metabolite ratio (VMR) (r(2)Exp = 0.582, p < 0.0001), and demonstrated a significant association with increasing PTH concentration (p < 0.001). Circannual rhythms were evident for all vitamin D metabolites and VMRs except for 1,25(OH)(2)D when fitted to Cosinor curves. We estimated 1,25(OH)(2)D:24,25(OH)(2)D VMR of ≥35 to be the threshold value for vitamin D insufficiency, and ≥51 to be predictive of vitamin D deficiency. Our three-dimensional model provides mechanistic insight into the vitamin D-PTH endocrine system, and further substantiates the role of 24,25(OH)(2)D in human physiology. The model sets a new paradigm for vitamin D treatment strategy, and may help the establishment of vitamin D-adjusted PTH reference intervals. The study was approved by the UK Ministry of Defence research ethics committee (MODREC 165/Gen/10 and 692/MoDREC/15). ClinicalTrials.gov Identifier NCT02416895. Nature Publishing Group UK 2019-05-06 /pmc/articles/PMC6502854/ /pubmed/31061425 http://dx.doi.org/10.1038/s41598-019-43462-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tang, Jonathan C. Y.
Jackson, Sarah
Walsh, Neil P.
Greeves, Julie
Fraser, William D.
The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH
title The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH
title_full The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH
title_fullStr The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH
title_full_unstemmed The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH
title_short The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH
title_sort dynamic relationships between the active and catabolic vitamin d metabolites, their ratios, and associations with pth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502854/
https://www.ncbi.nlm.nih.gov/pubmed/31061425
http://dx.doi.org/10.1038/s41598-019-43462-6
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