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1.
Osteoporos Int ; 28(11): 3205-3213, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28744601

ABSTRACT

The osteocyte's role in orchestrating diurnal variations in bone turnover markers (BTMs) is unclear. We identified no rhythm in serum sclerostin (osteocyte protein). These results suggest that serum sclerostin can be measured at any time of day and the osteocyte does not direct the rhythmicity of other BTMs in men. INTRODUCTION: The osteocyte exerts important effects on bone remodeling, but its rhythmicity and effect on the rhythms of other bone cells are not fully characterized. The purpose of this study was to determine if serum sclerostin displays rhythmicity over a 24-h interval, similar to that of other bone biomarkers. METHODS: Serum sclerostin, FGF-23, CTX, and P1NP were measured every 2 h over a 24-h interval in ten healthy men aged 20-65 years. Maximum likelihood estimates of the parameters in a repeated measures model were used to determine if these biomarkers displayed a diurnal, sinusoidal rhythm. RESULTS: No discernible 24-h rhythm was identified for sclerostin (p = 0.99) or P1NP (p = 0.65). CTX rhythmicity was confirmed (p < 0.001), peaking at 05:30 (range 01:30-07:30). FGF-23 levels were also rhythmic (p < 0.001), but time of peak was variable (range 02:30-11:30). The only significant association identified between these four bone biomarkers was for CTX and P1NP mean 24-h metabolite levels (r = 0.65, p = 0.04). CONCLUSIONS: Sclerostin levels do not appear to be rhythmic in men. This suggests that in contrast to CTX, serum sclerostin could be measured at any time of day. The 24-h profiles of FGF-23 suggest that a component of osteocyte function is rhythmic, but its timing is variable. Our results do not support the hypothesis that osteocytes direct the rhythmicity of other bone turnover markers (CTX), at least not via a sclerostin-mediated mechanism.


Subject(s)
Bone Morphogenetic Proteins/blood , Circadian Rhythm/physiology , Osteocytes/physiology , Adaptor Proteins, Signal Transducing , Adult , Aged , Biomarkers/blood , Blood Specimen Collection/methods , Bone Remodeling/physiology , Collagen Type I/blood , Fibroblast Growth Factor-23 , Fibroblast Growth Factors/blood , Genetic Markers , Humans , Male , Middle Aged , Peptide Fragments/blood , Peptides/blood , Procollagen/blood , Young Adult
2.
Pediatr Obes ; 11(3): 166-73, 2016 06.
Article in English | MEDLINE | ID: mdl-25988588

ABSTRACT

BACKGROUND: Individuals born at low or high birth weight (BW) have elevated adiposity. The extent to which physical activity can mitigate this risk is unknown. OBJECTIVES: The aim of this study was to determine if associations between BW and adiposity vary by self-reported moderate-to-vigorous physical activity (MVPA) among adolescents. METHODS: We used data on adolescents in the National Health and Nutrition Examination Survey (1999-2006; 12-15 years; n = 4064). Using gender-stratified linear regression, we modelled body mass index (BMI) and waist circumference (WC) z-scores as a function of low, normal and high BW, MVPA (weekly Metabolic Equivalent of Task hours) and MVPA*BW cross-product terms, adjusting for sociodemographics, diet and, in WC models, BMI. RESULTS: Among girls with low MVPA, those born with high BW had greater BMI than normal BW; this difference diminished with greater MVPA (coefficient [95% confidence interval]: low MVPA: 0.72 [0.29, 1.14]; high MVPA: -0.04 [-0.48, 0.39]; P for interaction = 0.05). Among boys, MVPA did not modify the associations between BW and BMI. WC was unrelated to BW, regardless of MVPA. CONCLUSIONS: Findings suggest that effects of high BW in total adiposity can be more easily modified with MVPA in adolescent girls than in boys.


Subject(s)
Adiposity , Birth Weight , Exercise , Adolescent , Body Mass Index , Child , Diet , Female , Humans , Male , Motor Activity , Nutrition Surveys , Obesity , Sex Factors , Waist Circumference
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