Näytä suppeat kuvailutiedot

dc.contributor.authorCheng, Sulin
dc.contributor.authorVölqyi, Eszter
dc.contributor.authorTylavsky, Frances A.
dc.contributor.authorLyytikäinen, Arja
dc.contributor.authorTörmäkangas, Timo
dc.contributor.authorXu, Leiting
dc.contributor.authorCheng, Shu Mei
dc.contributor.authorKröger, Heikki
dc.contributor.authorAlèn, Markku
dc.contributor.authorKujala, Urho M.
dc.date.accessioned2011-05-13T07:52:00Z
dc.date.available2011-05-13T07:52:00Z
dc.date.issued2009
dc.identifier.citationCheng, S., Völgyi, E., Tylavsky, F., Lyytikäinen, A., Törmäkangas, T., Xu, L., Cheng, S., Kröger, H., Alén, M. & Kujala, U. (2009). Trait-specific tracking and determinants of body composition: a 7-year follow-up study of pubertal growth in girls. BMC Medicine, 7. Retrieved from http://www.biomedcentral.com/1741-7015/7/5
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/26960
dc.description.abstractBACKGROUND: Understanding how bone (BM), lean (LM) and fat mass (FM) develop through childhood, puberty and adolescence is vital since it holds key information regarding current and future health. Our study aimed to determine how BM, LM and FM track from prepuberty to early adulthood in girls and what factors are associated with intra- and inter-individual variation in these three tissues. METHODS: The study was a 7-year longitudinal cohort study. BM, LM and FM measured using dual-energy X-ray absorptiometry, self-reported dietary information, leisure time physical activity (LTPA) and other factors were assessed one to eight times in 396 girls aged 10 to 13 years (baseline), and in 255 mothers once. RESULTS: The location of a girl's BM, LM and FM in the lower, middle or upper part of the sample distribution was established before puberty and tracked in its percentile of origin over 7 years (r = 0.72 for BM, r = 0.61 for LM, and r = 0.65 for FM all p < 0.001 first vs. last measurements' ranking). Seventy-three percent of those in the lowest quartile for BM and 69% for LM, and 79% of those in the highest quartile for FM at baseline remained in their quartile at 7-year follow-up. Heritability was estimated to contribute 69% of the total variance of the BM, 50% of the LM, and 57% of the FM. Besides body size, diet index (explaining 9% of variance), breast feeding duration (6%) and mother's BM (9%) predicted high BM. Diet index and high LTPA predicted high LM (24% and 14%, respectively), and low FM (25% and 12%, respectively), and low level of parental education predicted high FM (4%). CONCLUSION: Individual levels of BM, LM and FM are established before puberty and track in a trait-specific manner until early adulthood. Girls who are prone to develop low BM and LM and high FM in adulthood can be identified in prepuberty. The developments of three components of body composition are inter-related during growth. BM was the most heritable trait while LM the most environmentally modifiable. Diet and physical activity played an important role in increasing LM and preventing the accumulation of excessive FM.en
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.ispartofseriesBMC Medicine
dc.subject.othertrackingen
dc.subject.otherbody compositionen
dc.subject.othergrowthen
dc.subject.otheradolescenceen
dc.subject.otherkehon koostumusfi
dc.subject.otherkasvufi
dc.subject.otherliikuntafi
dc.subject.otherravintofi
dc.titleTrait-specific tracking and determinants of body composition: a 7-year follow-up study of pubertal growth in girls
dc.typejournal article
dc.identifier.urnURN:NBN:fi:jyu-2011051310799
dc.contributor.laitosTerveystieteiden laitosfi
dc.contributor.laitosDepartment of Health Sciencesen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_6501
dc.description.reviewstatuspeerReviewed
dc.relation.issn1741-7015
dc.type.versionpublishedVersion
dc.rights.copyright© 2009 Cheng et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.rights.urlhttp://creativecommons.org/licenses/by/2
dc.relation.doidoi:10.1186/1741-7015-7-5


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Näytä suppeat kuvailutiedot

© 2009 Cheng et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Ellei muuten mainita, aineiston lisenssi on © 2009 Cheng et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.