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Parathyroid hormone in relation to various vitamin D metabolites in adult females
Vitamin D binding protein (DBP) and albumin are the important determinants of circulatory 25(OH)D in adults. Physiological function of vitamin D is particularly regulated by DBPs. Serum parathyroid hormone (PTH) is considered as the biological activity reader of circulating 25(OH)D. We therefore exa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604675/ https://www.ncbi.nlm.nih.gov/pubmed/28906406 http://dx.doi.org/10.1097/MD.0000000000008071 |
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author | Al-Daghri, Nasser M. Yakout, Sobhy Bukhari, Ihtisham Khattak, Malak N.K. Al-Saleh, Yousef Aljohani, Naji Al-Attas, Omar S. Alokail, Majed |
author_facet | Al-Daghri, Nasser M. Yakout, Sobhy Bukhari, Ihtisham Khattak, Malak N.K. Al-Saleh, Yousef Aljohani, Naji Al-Attas, Omar S. Alokail, Majed |
author_sort | Al-Daghri, Nasser M. |
collection | PubMed |
description | Vitamin D binding protein (DBP) and albumin are the important determinants of circulatory 25(OH)D in adults. Physiological function of vitamin D is particularly regulated by DBPs. Serum parathyroid hormone (PTH) is considered as the biological activity reader of circulating 25(OH)D. We therefore examined the relationships between serum total, free, and bioavailable 25(OH)D versus PTH in apparently healthy Saudi female adults. A total of 350 apparently healthy Saudi female adults ([Mean ± standard deviation] age [years] 52.9 ± 9.2; body mass index [kg/m(2)] 32.9 ± 5.4) were included in this observational study. Anthropometrics was measured as well as fasting glucose, lipid profile, calcium and phosphorous using routine methods. Serum 25(OH)D was measured using an electrochemiluminescence immunoassay. Serum DBP was determined by ELISA. Free and bioavailable 25(OH)D were calculated by comparing concentrations of total 25(OH)D, DBP, and albumin. Data revealed that circulating total 25(OH)D had weak but significant inverse association with DBP (R = −0.24; P < .01), and strong inverse associations with free 25(OH)D (R = −0.87; P < .001), albumin-bound 25(OH)D (R = −0.88; P < .001), and bioavailable 25(OH)D (R = −0.89; p < 0.001). None of the vitamin D metabolites, including 25(OH)D, correlated with serum PTH. Various metabolites of 25(OH)D are not correlated with serum PTH in Saudi adult females. Bioavailable, albumin-bound and free 25(OH)D cannot be surrogate measures for vitamin D status, at least in this population. |
format | Online Article Text |
id | pubmed-5604675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-56046752017-10-03 Parathyroid hormone in relation to various vitamin D metabolites in adult females Al-Daghri, Nasser M. Yakout, Sobhy Bukhari, Ihtisham Khattak, Malak N.K. Al-Saleh, Yousef Aljohani, Naji Al-Attas, Omar S. Alokail, Majed Medicine (Baltimore) Research Article Vitamin D binding protein (DBP) and albumin are the important determinants of circulatory 25(OH)D in adults. Physiological function of vitamin D is particularly regulated by DBPs. Serum parathyroid hormone (PTH) is considered as the biological activity reader of circulating 25(OH)D. We therefore examined the relationships between serum total, free, and bioavailable 25(OH)D versus PTH in apparently healthy Saudi female adults. A total of 350 apparently healthy Saudi female adults ([Mean ± standard deviation] age [years] 52.9 ± 9.2; body mass index [kg/m(2)] 32.9 ± 5.4) were included in this observational study. Anthropometrics was measured as well as fasting glucose, lipid profile, calcium and phosphorous using routine methods. Serum 25(OH)D was measured using an electrochemiluminescence immunoassay. Serum DBP was determined by ELISA. Free and bioavailable 25(OH)D were calculated by comparing concentrations of total 25(OH)D, DBP, and albumin. Data revealed that circulating total 25(OH)D had weak but significant inverse association with DBP (R = −0.24; P < .01), and strong inverse associations with free 25(OH)D (R = −0.87; P < .001), albumin-bound 25(OH)D (R = −0.88; P < .001), and bioavailable 25(OH)D (R = −0.89; p < 0.001). None of the vitamin D metabolites, including 25(OH)D, correlated with serum PTH. Various metabolites of 25(OH)D are not correlated with serum PTH in Saudi adult females. Bioavailable, albumin-bound and free 25(OH)D cannot be surrogate measures for vitamin D status, at least in this population. Wolters Kluwer Health 2017-09-15 /pmc/articles/PMC5604675/ /pubmed/28906406 http://dx.doi.org/10.1097/MD.0000000000008071 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Research Article Al-Daghri, Nasser M. Yakout, Sobhy Bukhari, Ihtisham Khattak, Malak N.K. Al-Saleh, Yousef Aljohani, Naji Al-Attas, Omar S. Alokail, Majed Parathyroid hormone in relation to various vitamin D metabolites in adult females |
title | Parathyroid hormone in relation to various vitamin D metabolites in adult females |
title_full | Parathyroid hormone in relation to various vitamin D metabolites in adult females |
title_fullStr | Parathyroid hormone in relation to various vitamin D metabolites in adult females |
title_full_unstemmed | Parathyroid hormone in relation to various vitamin D metabolites in adult females |
title_short | Parathyroid hormone in relation to various vitamin D metabolites in adult females |
title_sort | parathyroid hormone in relation to various vitamin d metabolites in adult females |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604675/ https://www.ncbi.nlm.nih.gov/pubmed/28906406 http://dx.doi.org/10.1097/MD.0000000000008071 |
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