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Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty

BACKGROUND: We investigated longitudinal relationships between the biochemical markers of bone and adipose tissue with bone mineral content (BMC), bone mineral density (BMD), moderate-to-vigorous physical activity (MVPA) and sedentary time (SED) in pubertal boys. METHODS: Ninety-six boys (11.9 ± 0.6...

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Autores principales: Vaitkeviciute, Donvina, Lätt, Evelin, Mäestu, Jarek, Jürimäe, Toivo, Saar, Meeli, Purge, Priit, Maasalu, Katre, Jürimäe, Jaak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955269/
https://www.ncbi.nlm.nih.gov/pubmed/27439435
http://dx.doi.org/10.1186/s12887-016-0647-1
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author Vaitkeviciute, Donvina
Lätt, Evelin
Mäestu, Jarek
Jürimäe, Toivo
Saar, Meeli
Purge, Priit
Maasalu, Katre
Jürimäe, Jaak
author_facet Vaitkeviciute, Donvina
Lätt, Evelin
Mäestu, Jarek
Jürimäe, Toivo
Saar, Meeli
Purge, Priit
Maasalu, Katre
Jürimäe, Jaak
author_sort Vaitkeviciute, Donvina
collection PubMed
description BACKGROUND: We investigated longitudinal relationships between the biochemical markers of bone and adipose tissue with bone mineral content (BMC), bone mineral density (BMD), moderate-to-vigorous physical activity (MVPA) and sedentary time (SED) in pubertal boys. METHODS: Ninety-six boys (11.9 ± 0.6 years old) were measured at baseline, after 12 and 24 months. Body composition (fat mass [FM], lean body mass [LBM]), and whole body (WB), lumbar spine (LS) and femoral neck (FN) BMD and BMC were assessed. Additionally, serum leptin, adiponectin, osteocalcin (OC) and C-terminal telopeptide of type I collagen (CTX) were measured. RESULTS: OC had a strong longitudinal inverse effect on changes in WB_BMD (p < 0.001) and LS_BMD (p = 0.021), while CTX had an inverse effect only on changes in FN_BMD (p = 0.011). Leptin had an inverse effect on changes in WB_BMC/WB_BMD (p = 0.001), FN_BMD (p = 0.002) and LS_BMD (p = 0.001). MVPA showed a longitudinal inverse effect on changes in leptin (p = 0.030), however no longitudinal effect of SED to biochemical markers of bone and adipose tissue was found. CONCLUSIONS: Bone metabolism markers have negative effect on bone mineral accrual during puberty. Increases in MVPA affect leptin, suggesting a positive link of MVPA through leptin metabolism on increases in bone mineralization during puberty.
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spelling pubmed-49552692016-07-22 Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty Vaitkeviciute, Donvina Lätt, Evelin Mäestu, Jarek Jürimäe, Toivo Saar, Meeli Purge, Priit Maasalu, Katre Jürimäe, Jaak BMC Pediatr Research Article BACKGROUND: We investigated longitudinal relationships between the biochemical markers of bone and adipose tissue with bone mineral content (BMC), bone mineral density (BMD), moderate-to-vigorous physical activity (MVPA) and sedentary time (SED) in pubertal boys. METHODS: Ninety-six boys (11.9 ± 0.6 years old) were measured at baseline, after 12 and 24 months. Body composition (fat mass [FM], lean body mass [LBM]), and whole body (WB), lumbar spine (LS) and femoral neck (FN) BMD and BMC were assessed. Additionally, serum leptin, adiponectin, osteocalcin (OC) and C-terminal telopeptide of type I collagen (CTX) were measured. RESULTS: OC had a strong longitudinal inverse effect on changes in WB_BMD (p < 0.001) and LS_BMD (p = 0.021), while CTX had an inverse effect only on changes in FN_BMD (p = 0.011). Leptin had an inverse effect on changes in WB_BMC/WB_BMD (p = 0.001), FN_BMD (p = 0.002) and LS_BMD (p = 0.001). MVPA showed a longitudinal inverse effect on changes in leptin (p = 0.030), however no longitudinal effect of SED to biochemical markers of bone and adipose tissue was found. CONCLUSIONS: Bone metabolism markers have negative effect on bone mineral accrual during puberty. Increases in MVPA affect leptin, suggesting a positive link of MVPA through leptin metabolism on increases in bone mineralization during puberty. BioMed Central 2016-07-20 /pmc/articles/PMC4955269/ /pubmed/27439435 http://dx.doi.org/10.1186/s12887-016-0647-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Vaitkeviciute, Donvina
Lätt, Evelin
Mäestu, Jarek
Jürimäe, Toivo
Saar, Meeli
Purge, Priit
Maasalu, Katre
Jürimäe, Jaak
Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
title Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
title_full Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
title_fullStr Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
title_full_unstemmed Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
title_short Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
title_sort longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955269/
https://www.ncbi.nlm.nih.gov/pubmed/27439435
http://dx.doi.org/10.1186/s12887-016-0647-1
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