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dc.contributor.authorConstable, Annie M.
dc.contributor.authorVlachopoulos, Dimitris
dc.contributor.authorBarker, Alan R.
dc.contributor.authorMoore, Sarah A.
dc.contributor.authorSoininen, Sonja
dc.contributor.authorHaapala, Eero A.
dc.contributor.authorVäistö, Juuso
dc.contributor.authorJääskeläinen, Jarmo
dc.contributor.authorVoutilainen, Raimo
dc.contributor.authorAuriola, Seppo
dc.contributor.authorHäkkinen, Merja R.
dc.contributor.authorLaitinen, Tomi
dc.contributor.authorLakka, Timo A.
dc.date.accessioned2022-06-16T10:41:21Z
dc.date.available2022-06-16T10:41:21Z
dc.date.issued2022
dc.identifier.citationConstable, A. M., Vlachopoulos, D., Barker, A. R., Moore, S. A., Soininen, S., Haapala, E. A., Väistö, J., Jääskeläinen, J., Voutilainen, R., Auriola, S., Häkkinen, M. R., Laitinen, T., & Lakka, T. A. (2022). The Mediating Role of Endocrine Factors in the Positive Relationship Between Fat Mass and Bone Mineral Content in Children Aged 9–11 Years : The Physical Activity and Nutrition in Children Study. <i>Frontiers in Endocrinology</i>, <i>13</i>, Article 850448. <a href="https://doi.org/10.3389/fendo.2022.850448" target="_blank">https://doi.org/10.3389/fendo.2022.850448</a>
dc.identifier.otherCONVID_146492264
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/81812
dc.description.abstractIntroduction: We aimed to investigate whether the relationship between fat mass and bone mineral content (BMC) is mediated by insulin, leptin, adiponectin, dehydroepiandrosterone sulphate, testosterone and estradiol in children aged 9-11 years. Materials and Methods: We utilised cross-sectional data from the Physical Activity and Nutrition in Children study (n = 230 to 396; 112 to 203 girls). Fat mass and BMC were assessed with dual-energy X-ray absorptiometry. Endocrine factors were assessed from fasted blood samples. We applied the novel 4-way decomposition method to analyse associations between fat mass, endocrine factors, and BMC. Results: Fat mass was positively associated with BMC in girls (ß = 0.007 to 0.015, 95% confidence interval (CI) 0.005 to 0.020) and boys (ß = 0.009 to 0.015, 95% CI 0.005 to 0.019). The relationship between fat mass and BMC was mediated by free leptin index in girls (ß = -0.025, 95% CI -0.039 to -0.010) and boys (ß = -0.014, 95% CI -0.027 to -0.001). The relationship between fat mass and BMC was partially explained by mediated interaction between fat mass and free leptin index in boys (ß = -0.009, 95% CI -0.013 to -0.004) and by interaction between fat mass and adiponectin in girls (ß = -0.003, 95% CI -0.006 to -0.000). Conclusion: At greater levels of adiponectin and free leptin index, the fat mass and BMC relationship becomes less positive in girls and boys respectively. The positive association between fat mass with BMC was largely not explained by the endocrine factors we assessed.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherFrontiers Media SA
dc.relation.ispartofseriesFrontiers in Endocrinology
dc.rightsCC BY 4.0
dc.subject.otheradiposity
dc.subject.otherinsulin
dc.subject.otherleptin
dc.subject.otheradiponectin
dc.subject.otherDXA (dual-energy X-ray absorptiometry)
dc.subject.otherpaediatric
dc.titleThe Mediating Role of Endocrine Factors in the Positive Relationship Between Fat Mass and Bone Mineral Content in Children Aged 9–11 Years : The Physical Activity and Nutrition in Children Study
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202206163421
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineLiikuntalääketiedefi
dc.contributor.oppiaineBiomekaniikkafi
dc.contributor.oppiaineSports and Exercise Medicineen
dc.contributor.oppiaineBiomechanicsen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1664-2392
dc.relation.volume13
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 the Authors
dc.rights.accesslevelopenAccessfi
dc.subject.ysoleptiini
dc.subject.ysorasvakudokset
dc.subject.ysokehonkoostumus
dc.subject.ysolapset (ikäryhmät)
dc.subject.ysohormonaaliset tekijät
dc.subject.ysoinsuliini
dc.subject.ysoadiponektiini
dc.subject.ysoluuntiheys
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p11607
jyx.subject.urihttp://www.yso.fi/onto/yso/p24382
jyx.subject.urihttp://www.yso.fi/onto/yso/p26989
jyx.subject.urihttp://www.yso.fi/onto/yso/p4354
jyx.subject.urihttp://www.yso.fi/onto/yso/p21658
jyx.subject.urihttp://www.yso.fi/onto/yso/p8422
jyx.subject.urihttp://www.yso.fi/onto/yso/p23953
jyx.subject.urihttp://www.yso.fi/onto/yso/p22879
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.3389/fendo.2022.850448
jyx.fundinginformationThis work was financially supported by grants from Ministry of Social Affairs and Health of Finland, Ministry of Education and Culture of Finland, Finnish Innovation Fund Sitra, Social Insurance Institution of Finland, Finnish Cultural Foundation, Juho Vainio Foundation (application number: 202100397), Foundation for Paediatric Research, Doctoral Programs in Public Health, Paavo Nurmi Foundation, Paulo Foundation, Diabetes Research Foundation, The Finnish Medical Society Duodecim, Orion Research Foundation sr, Research Committee of the Kuopio University Hospital Catchment Area (State Research Funding), Kuopio University Hospital (previous state research funding (EVO), funding number 5031343) and the city of Kuopio. The UEF LC-MS Metabolomics laboratory is supported by Biocenter Finland and Biocenter Kuopio. The open access publication fees were supported by the University of Exeter.
dc.type.okmA1


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