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    Relative contributions of lean and fat mass to bone strength in young Hispanic and non-Hispanic girls

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    Name:
    Fat_Distribution_and_Risk_Am_J ...
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    Description:
    Final Accepted Manuscript
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    Author
    Hetherington-Rauth, Megan cc
    Bea, Jennifer W.
    Blew, Robert M.
    Funk, Janet L.
    Hingle, Melanie D.
    Lee, Vinson R.
    Roe, Denise J.
    Wheeler, Mark D.
    Lohman, Timothy G.
    Going, Scott B.
    Affiliation
    Univ Arizona, Dept Nutr Sci
    Univ Arizona, Dept Med
    Univ Arizona, Dept Epidemiol & Biostat
    Univ Arizona, Dept Pediat Endocrinol
    Issue Date
    2018-08
    Keywords
    Lean mass
    Fat mass
    Girls
    Bone strength
    Peripheral quantitative computed tomography (pQCT)
    Hispanic
    
    Metadata
    Show full item record
    Publisher
    ELSEVIER SCIENCE INC
    Citation
    Hetherington-Rauth, M., Bea, J. W., Blew, R. M., Funk, J. L., Hingle, M. D., Lee, V. R., ... & Going, S. B. (2018). Relative contributions of lean and fat mass to bone strength in young Hispanic and non-Hispanic girls. Bone, 113, 144-150. https://doi.org/10.1016/j.bone.2018.05.023
    Journal
    BONE
    Rights
    © 2018 Elsevier Inc. All rights reserved.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Background: With the high prevalence of childhood obesity, especially among Hispanic children, understanding how body weight and its components of lean and fat mass affect bone development is important, given that the amount of bone mineral accrued during childhood can determine osteoporosis risk later in life. The aim of this study was to assess the independent contributions of lean and fat mass on volumetric bone mineral density (vBMD), geometry, and strength in both weight-bearing and non-weight-bearing bones of Hispanic and non-Hispanic girls. Methods: Bone vBMD, geometry, and strength were assessed at the 20% distal femur, the 4% and 66% distal tibia, and the 66% distal radius of the non-dominant limb of 326, 9- to 12-year-old girls using peripheral quantitative computed tomography (pQCT). Total body lean and fat mass were measured by dual-energy x-ray absorptiometry (DXA). Multiple linear regression was used to assess the independent relationships of fat and lean mass with pQCT bone measures while adjusting for relevant confounders. Potential interactions between ethnicity and both fat and lean mass were also tested. Results: Lean mass was a significant positive contributor to all bone outcomes (p < 0.05) with the exception of vBMD at diaphyseal sites. Fat mass was a significant contributor to bone strength at weight bearing sites, but did not significantly contribute to bone strength at the non-weight bearing radius and was negatively associated with radius cortical content and thickness. Bone measures did not significantly differ between Hispanic and non-Hispanic girls, although there was a significant interaction between ethnicity and fat mass with total bone area at the femur (p = 0.02) and 66% tibia (p = 0.005) as well as bone strength at the femur (p = 0.03). Conclusion: Lean mass is the main determinant of bone strength for appendicular skeletal sites. Fat mass contributes to bone strength in the weight-bearing skeleton but does not add to bone strength in non-weight-bearing locations and may potentially be detrimental. Bone vBMD, geometry, and strength did not differ between Hispanic and non-Hispanic girls; fat mass may be a stronger contributor to bone strength in weight-bearing bones of Hispanic girls compared to non-Hispanic.
    Note
    12 month embargo; published online: 22 May 2018
    ISSN
    87563282
    PubMed ID
    29800691
    DOI
    10.1016/j.bone.2018.05.023
    Version
    Final accepted manuscript
    Sponsors
    National Institute of Child Health and Human Development [HD074565]
    Additional Links
    https://linkinghub.elsevier.com/retrieve/pii/S8756328218302138
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.bone.2018.05.023
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