Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
Calcif Tissue Int. 2019 Jun;104(6):605-612. doi: 10.1007/s00223-019-00529-w. Epub 2019 Feb 1.
This study aimed to describe the association of vitamin D status at different stages of growth with bone measures in adolescence and early adulthood. There were 415 participants followed from age 8 to 16, and 201 further followed to age 25. Areal bone mineral density (BMD) at the spine, hip and total body was measured by dual-energy X-ray absorptiometry at ages 16 and 25, and tibial and radial trabecular and cortical bone microarchitecture by high resolution peripheral quantitative computerised tomography at age 25. Serum 25-hydroxyvitamin D (25OHD) concentrations were measured at ages 8, 16 and 25. Multivariable linear regression was used to analyse the association of 25OHD concentrations at three timepoints with bone measures at ages 16 and 25. The proportion of participants with vitamin D deficiency (< 50 nmol/L) was 11%, 43% and 41% at three timepoints, respectively. Serum 25OHD concentrations at age 8 were not significantly associated with any bone measures at age 16 or 25. Serum 25OHD concentrations at age 16 had a significant association with higher BMD at nearly all sites at ages 16 and 25 as well as lower radial porosity and more compact trabecular microarchitecture (higher density, increased number and reduced separation) at both the radius and tibia at age 25. Serum 25OHD concentrations at age 25 were only associated with hip BMD. Higher vitamin D concentrations in adolescence, to a lesser extent at age 25, have beneficial associations with BMD and bone microarchitecture in early adulthood. Optimising vitamin D status particularly during adolescence should be a priority.
本研究旨在描述不同生长阶段维生素 D 状态与青少年和成年早期骨骼指标的关系。共有 415 名参与者从 8 岁随访至 16 岁,其中 201 名进一步随访至 25 岁。在 16 岁和 25 岁时,通过双能 X 射线吸收法测量脊柱、髋部和全身的骨矿物质密度(BMD),在 25 岁时,通过高分辨率外周定量计算机断层扫描测量胫骨和桡骨的小梁和皮质骨微观结构。在 8、16 和 25 岁时测量血清 25-羟维生素 D(25OHD)浓度。使用多变量线性回归分析 3 个时间点的 25OHD 浓度与 16 岁和 25 岁时的骨骼指标之间的关系。在这 3 个时间点,维生素 D 缺乏症(<50nmol/L)的参与者比例分别为 11%、43%和 41%。8 岁时的血清 25OHD 浓度与 16 岁或 25 岁时的任何骨骼指标均无显著相关性。16 岁时的血清 25OHD 浓度与 16 岁和 25 岁时几乎所有部位的 BMD 升高以及桡骨和胫骨的骨小梁孔隙率降低和更致密的小梁微观结构(更高的密度、增加的数量和减少的分离)显著相关。25 岁时的血清 25OHD 浓度仅与髋部 BMD 相关。青少年时期较高的维生素 D 浓度,在一定程度上在 25 岁时,与成年早期的 BMD 和骨微观结构有有益的关联。特别是在青少年时期优化维生素 D 状态应是优先事项。