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

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. Ninety-six boys (11.9 ± 0.6 years old) were meas...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:BMC pediatrics 2016-07, Vol.16 (1), p.102-102, Article 102
Hauptverfasser: Vaitkeviciute, Donvina, Lätt, Evelin, Mäestu, Jarek, Jürimäe, Toivo, Saar, Meeli, Purge, Priit, Maasalu, Katre, Jürimäe, Jaak
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 102
container_issue 1
container_start_page 102
container_title BMC pediatrics
container_volume 16
creator Vaitkeviciute, Donvina
Lätt, Evelin
Mäestu, Jarek
Jürimäe, Toivo
Saar, Meeli
Purge, Priit
Maasalu, Katre
Jürimäe, Jaak
description 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. 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. OC had a strong longitudinal inverse effect on changes in WB_BMD (p 
doi_str_mv 10.1186/s12887-016-0647-1
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4955269</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A468888279</galeid><sourcerecordid>A468888279</sourcerecordid><originalsourceid>FETCH-LOGICAL-c486t-a35721e517a72122b7cd3aa23bf8b69314486edf08de52f43d1be6b01d07cc833</originalsourceid><addsrcrecordid>eNpdkk2LFDEQhoMo7jr6A7xIQBAvrfnqTuYiLItfMOBFzyGdVE9n7U7GTnqXEfzvpmfWYdZcKpCn3qpUvQi9pOQdpap5nyhTSlaENhVphKzoI3RJhaQVE5w-PrtfoGcp3RBCpRLNU3TBpOBrwetL9GcTw9bn2flgBmxSitab7GNIuIV8BxBwGwNgExw2zu9iApx9SjPg1kfbw-htSRzN9BOmhO987o8Jow8wmcH_Pqhhv-jsE3bz5MMW7-YWprx_jp50Zkjw4j6u0I9PH79ff6k23z5_vb7aVFaoJleG15JRqKk0JTLWSuu4MYy3nWqbNaeiYOA6ohzUrBPc0RaallBHpLWK8xX6cNQtdUdwFkIuvend5Evjex2N1w9fgu_1Nt5qsa5rViqs0Nt7gSn-miFlPfpkYRhMgDgnTVVZAJeCiIK-_g-9ifNUpnugFF3zBT1RWzOA9qGLpa5dRPWVaFQ5TC5l35xRPZgh9ykO82FBD0F6BO0UU5qgO_2NEr14RR-9ootX9OIVTUvOq_OhnDL-mYP_Baliu8Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1808193064</pqid></control><display><type>article</type><title>Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>SpringerLink Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Springer Nature OA/Free Journals</source><source>PubMed Central Open Access</source><creator>Vaitkeviciute, Donvina ; Lätt, Evelin ; Mäestu, Jarek ; Jürimäe, Toivo ; Saar, Meeli ; Purge, Priit ; Maasalu, Katre ; Jürimäe, Jaak</creator><creatorcontrib>Vaitkeviciute, Donvina ; Lätt, Evelin ; Mäestu, Jarek ; Jürimäe, Toivo ; Saar, Meeli ; Purge, Priit ; Maasalu, Katre ; Jürimäe, Jaak</creatorcontrib><description>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. 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. OC had a strong longitudinal inverse effect on changes in WB_BMD (p &lt; 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. 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.</description><identifier>ISSN: 1471-2431</identifier><identifier>EISSN: 1471-2431</identifier><identifier>DOI: 10.1186/s12887-016-0647-1</identifier><identifier>PMID: 27439435</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adiponectin - blood ; Adiposity - physiology ; Adolescent ; Analysis ; Biological markers ; Biomarkers - blood ; Body composition ; Body fat ; Bone Density - physiology ; Bone Remodeling - physiology ; Bones ; Calcification ; Child ; Children ; Children &amp; youth ; Collagen Type I - blood ; Density ; Exercise ; Exercise - physiology ; Health aspects ; Humans ; Leptin - blood ; Longitudinal Studies ; Male ; Males ; Mineralization ; Models, Statistical ; Osteocalcin - blood ; Peptides - blood ; Puberty ; Puberty - blood ; Puberty - physiology ; Sedentary Lifestyle ; Software ; Statistical analysis ; Teenagers ; Variance analysis</subject><ispartof>BMC pediatrics, 2016-07, Vol.16 (1), p.102-102, Article 102</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-a35721e517a72122b7cd3aa23bf8b69314486edf08de52f43d1be6b01d07cc833</citedby><cites>FETCH-LOGICAL-c486t-a35721e517a72122b7cd3aa23bf8b69314486edf08de52f43d1be6b01d07cc833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955269/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955269/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27439435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vaitkeviciute, Donvina</creatorcontrib><creatorcontrib>Lätt, Evelin</creatorcontrib><creatorcontrib>Mäestu, Jarek</creatorcontrib><creatorcontrib>Jürimäe, Toivo</creatorcontrib><creatorcontrib>Saar, Meeli</creatorcontrib><creatorcontrib>Purge, Priit</creatorcontrib><creatorcontrib>Maasalu, Katre</creatorcontrib><creatorcontrib>Jürimäe, Jaak</creatorcontrib><title>Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty</title><title>BMC pediatrics</title><addtitle>BMC Pediatr</addtitle><description>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. 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. OC had a strong longitudinal inverse effect on changes in WB_BMD (p &lt; 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. 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.</description><subject>Adiponectin - blood</subject><subject>Adiposity - physiology</subject><subject>Adolescent</subject><subject>Analysis</subject><subject>Biological markers</subject><subject>Biomarkers - blood</subject><subject>Body composition</subject><subject>Body fat</subject><subject>Bone Density - physiology</subject><subject>Bone Remodeling - physiology</subject><subject>Bones</subject><subject>Calcification</subject><subject>Child</subject><subject>Children</subject><subject>Children &amp; youth</subject><subject>Collagen Type I - blood</subject><subject>Density</subject><subject>Exercise</subject><subject>Exercise - physiology</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Leptin - blood</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Males</subject><subject>Mineralization</subject><subject>Models, Statistical</subject><subject>Osteocalcin - blood</subject><subject>Peptides - blood</subject><subject>Puberty</subject><subject>Puberty - blood</subject><subject>Puberty - physiology</subject><subject>Sedentary Lifestyle</subject><subject>Software</subject><subject>Statistical analysis</subject><subject>Teenagers</subject><subject>Variance analysis</subject><issn>1471-2431</issn><issn>1471-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkk2LFDEQhoMo7jr6A7xIQBAvrfnqTuYiLItfMOBFzyGdVE9n7U7GTnqXEfzvpmfWYdZcKpCn3qpUvQi9pOQdpap5nyhTSlaENhVphKzoI3RJhaQVE5w-PrtfoGcp3RBCpRLNU3TBpOBrwetL9GcTw9bn2flgBmxSitab7GNIuIV8BxBwGwNgExw2zu9iApx9SjPg1kfbw-htSRzN9BOmhO987o8Jow8wmcH_Pqhhv-jsE3bz5MMW7-YWprx_jp50Zkjw4j6u0I9PH79ff6k23z5_vb7aVFaoJleG15JRqKk0JTLWSuu4MYy3nWqbNaeiYOA6ohzUrBPc0RaallBHpLWK8xX6cNQtdUdwFkIuvend5Evjex2N1w9fgu_1Nt5qsa5rViqs0Nt7gSn-miFlPfpkYRhMgDgnTVVZAJeCiIK-_g-9ifNUpnugFF3zBT1RWzOA9qGLpa5dRPWVaFQ5TC5l35xRPZgh9ykO82FBD0F6BO0UU5qgO_2NEr14RR-9ootX9OIVTUvOq_OhnDL-mYP_Baliu8Q</recordid><startdate>20160720</startdate><enddate>20160720</enddate><creator>Vaitkeviciute, Donvina</creator><creator>Lätt, Evelin</creator><creator>Mäestu, Jarek</creator><creator>Jürimäe, Toivo</creator><creator>Saar, Meeli</creator><creator>Purge, Priit</creator><creator>Maasalu, Katre</creator><creator>Jürimäe, Jaak</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160720</creationdate><title>Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty</title><author>Vaitkeviciute, Donvina ; Lätt, Evelin ; Mäestu, Jarek ; Jürimäe, Toivo ; Saar, Meeli ; Purge, Priit ; Maasalu, Katre ; Jürimäe, Jaak</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-a35721e517a72122b7cd3aa23bf8b69314486edf08de52f43d1be6b01d07cc833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adiponectin - blood</topic><topic>Adiposity - physiology</topic><topic>Adolescent</topic><topic>Analysis</topic><topic>Biological markers</topic><topic>Biomarkers - blood</topic><topic>Body composition</topic><topic>Body fat</topic><topic>Bone Density - physiology</topic><topic>Bone Remodeling - physiology</topic><topic>Bones</topic><topic>Calcification</topic><topic>Child</topic><topic>Children</topic><topic>Children &amp; youth</topic><topic>Collagen Type I - blood</topic><topic>Density</topic><topic>Exercise</topic><topic>Exercise - physiology</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Leptin - blood</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Males</topic><topic>Mineralization</topic><topic>Models, Statistical</topic><topic>Osteocalcin - blood</topic><topic>Peptides - blood</topic><topic>Puberty</topic><topic>Puberty - blood</topic><topic>Puberty - physiology</topic><topic>Sedentary Lifestyle</topic><topic>Software</topic><topic>Statistical analysis</topic><topic>Teenagers</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vaitkeviciute, Donvina</creatorcontrib><creatorcontrib>Lätt, Evelin</creatorcontrib><creatorcontrib>Mäestu, Jarek</creatorcontrib><creatorcontrib>Jürimäe, Toivo</creatorcontrib><creatorcontrib>Saar, Meeli</creatorcontrib><creatorcontrib>Purge, Priit</creatorcontrib><creatorcontrib>Maasalu, Katre</creatorcontrib><creatorcontrib>Jürimäe, Jaak</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vaitkeviciute, Donvina</au><au>Lätt, Evelin</au><au>Mäestu, Jarek</au><au>Jürimäe, Toivo</au><au>Saar, Meeli</au><au>Purge, Priit</au><au>Maasalu, Katre</au><au>Jürimäe, Jaak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty</atitle><jtitle>BMC pediatrics</jtitle><addtitle>BMC Pediatr</addtitle><date>2016-07-20</date><risdate>2016</risdate><volume>16</volume><issue>1</issue><spage>102</spage><epage>102</epage><pages>102-102</pages><artnum>102</artnum><issn>1471-2431</issn><eissn>1471-2431</eissn><abstract>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. 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. OC had a strong longitudinal inverse effect on changes in WB_BMD (p &lt; 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. 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.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27439435</pmid><doi>10.1186/s12887-016-0647-1</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1471-2431
ispartof BMC pediatrics, 2016-07, Vol.16 (1), p.102-102, Article 102
issn 1471-2431
1471-2431
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4955269
source MEDLINE; DOAJ Directory of Open Access Journals; SpringerLink Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Springer Nature OA/Free Journals; PubMed Central Open Access
subjects Adiponectin - blood
Adiposity - physiology
Adolescent
Analysis
Biological markers
Biomarkers - blood
Body composition
Body fat
Bone Density - physiology
Bone Remodeling - physiology
Bones
Calcification
Child
Children
Children & youth
Collagen Type I - blood
Density
Exercise
Exercise - physiology
Health aspects
Humans
Leptin - blood
Longitudinal Studies
Male
Males
Mineralization
Models, Statistical
Osteocalcin - blood
Peptides - blood
Puberty
Puberty - blood
Puberty - physiology
Sedentary Lifestyle
Software
Statistical analysis
Teenagers
Variance analysis
title Longitudinal associations between bone and adipose tissue biochemical markers with bone mineralization in boys during puberty
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T07%3A07%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Longitudinal%20associations%20between%20bone%20and%20adipose%20tissue%20biochemical%20markers%20with%20bone%20mineralization%20in%20boys%20during%20puberty&rft.jtitle=BMC%20pediatrics&rft.au=Vaitkeviciute,%20Donvina&rft.date=2016-07-20&rft.volume=16&rft.issue=1&rft.spage=102&rft.epage=102&rft.pages=102-102&rft.artnum=102&rft.issn=1471-2431&rft.eissn=1471-2431&rft_id=info:doi/10.1186/s12887-016-0647-1&rft_dat=%3Cgale_pubme%3EA468888279%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1808193064&rft_id=info:pmid/27439435&rft_galeid=A468888279&rfr_iscdi=true