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Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups

CONTEXT: Ethnic groups differ in fragility fracture risk and bone metabolism. Differences in diurnal rhythms (DRs) of bone turnover and PTH may play a role. OBJECTIVE: We investigated the DRs of plasma bone turnover markers (BTMs), PTH, and 1,25(OH)(2)D in three groups with pronounced differences in...

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Autores principales: Redmond, Jean, Fulford, Anthony J., Jarjou, Landing, Zhou, Bo, Prentice, Ann, Schoenmakers, Inez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971334/
https://www.ncbi.nlm.nih.gov/pubmed/27294326
http://dx.doi.org/10.1210/jc.2016-1183
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author Redmond, Jean
Fulford, Anthony J.
Jarjou, Landing
Zhou, Bo
Prentice, Ann
Schoenmakers, Inez
author_facet Redmond, Jean
Fulford, Anthony J.
Jarjou, Landing
Zhou, Bo
Prentice, Ann
Schoenmakers, Inez
author_sort Redmond, Jean
collection PubMed
description CONTEXT: Ethnic groups differ in fragility fracture risk and bone metabolism. Differences in diurnal rhythms (DRs) of bone turnover and PTH may play a role. OBJECTIVE: We investigated the DRs of plasma bone turnover markers (BTMs), PTH, and 1,25(OH)(2)D in three groups with pronounced differences in bone metabolism and plasma PTH. PARTICIPANTS: Healthy Gambian, Chinese, and white British adults (ages 60–75 years; 30 per country). INTERVENTIONS: Observational study with sample collection every 4 hours for 24 hours. MAIN OUTCOMES: Levels of plasma C-terminal telopeptide of type I collagen, procollagen type-1 N-propeptide, N-mid osteocalcin, bone alkaline phosphatase, PTH, and 1,25-dihydroxyvitamin D were measured. DRs were analyzed with random-effects Fourier regression and cross-correlation and regression analyses to assess associations between DRs and fasting and 24-hour means of BTMs and PTH. RESULTS: Concentrations of BTMs, PTH, and 1,25-dihydroxyvitamin D were higher in Gambians compared to other groups (P < .05). The DRs were significant for all variables and groups (P < .03) and were unimodal, with a nocturnal peak and a daytime nadir for BTMs, whereas PTH had two peaks. The DRs of BTMs and PTH were significantly cross-correlated for all groups (P < .05). There was a significant positive association between C-terminal telopeptide of type I collagen and PTH in the British and Gambian groups (P = .03), but not the Chinese group. CONCLUSIONS: Despite ethnic differences in plasma BTMs and PTH, DRs were similar. This indicates that alteration of rhythmicity and loss of coupling of bone resorption and formation associated with an elevated PTH in other studies may not uniformly occur across different populations and needs to be considered in the interpretation of PTH as a risk factor of increased bone loss.
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spelling pubmed-49713342016-08-17 Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups Redmond, Jean Fulford, Anthony J. Jarjou, Landing Zhou, Bo Prentice, Ann Schoenmakers, Inez J Clin Endocrinol Metab Original Articles CONTEXT: Ethnic groups differ in fragility fracture risk and bone metabolism. Differences in diurnal rhythms (DRs) of bone turnover and PTH may play a role. OBJECTIVE: We investigated the DRs of plasma bone turnover markers (BTMs), PTH, and 1,25(OH)(2)D in three groups with pronounced differences in bone metabolism and plasma PTH. PARTICIPANTS: Healthy Gambian, Chinese, and white British adults (ages 60–75 years; 30 per country). INTERVENTIONS: Observational study with sample collection every 4 hours for 24 hours. MAIN OUTCOMES: Levels of plasma C-terminal telopeptide of type I collagen, procollagen type-1 N-propeptide, N-mid osteocalcin, bone alkaline phosphatase, PTH, and 1,25-dihydroxyvitamin D were measured. DRs were analyzed with random-effects Fourier regression and cross-correlation and regression analyses to assess associations between DRs and fasting and 24-hour means of BTMs and PTH. RESULTS: Concentrations of BTMs, PTH, and 1,25-dihydroxyvitamin D were higher in Gambians compared to other groups (P < .05). The DRs were significant for all variables and groups (P < .03) and were unimodal, with a nocturnal peak and a daytime nadir for BTMs, whereas PTH had two peaks. The DRs of BTMs and PTH were significantly cross-correlated for all groups (P < .05). There was a significant positive association between C-terminal telopeptide of type I collagen and PTH in the British and Gambian groups (P = .03), but not the Chinese group. CONCLUSIONS: Despite ethnic differences in plasma BTMs and PTH, DRs were similar. This indicates that alteration of rhythmicity and loss of coupling of bone resorption and formation associated with an elevated PTH in other studies may not uniformly occur across different populations and needs to be considered in the interpretation of PTH as a risk factor of increased bone loss. Endocrine Society 2016-08 2016-06-13 /pmc/articles/PMC4971334/ /pubmed/27294326 http://dx.doi.org/10.1210/jc.2016-1183 Text en https://creativecommons.org/licenses/by/4.0/ This article has been published under the terms of the Creative Commons Attribution License (CC-BY; https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s).
spellingShingle Original Articles
Redmond, Jean
Fulford, Anthony J.
Jarjou, Landing
Zhou, Bo
Prentice, Ann
Schoenmakers, Inez
Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups
title Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups
title_full Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups
title_fullStr Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups
title_full_unstemmed Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups
title_short Diurnal Rhythms of Bone Turnover Markers in Three Ethnic Groups
title_sort diurnal rhythms of bone turnover markers in three ethnic groups
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971334/
https://www.ncbi.nlm.nih.gov/pubmed/27294326
http://dx.doi.org/10.1210/jc.2016-1183
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