Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Department of Endocrinology, Auckland District Health Board, Auckland, New Zealand.
J Intern Med. 2017 Nov;282(5):452-460. doi: 10.1111/joim.12651. Epub 2017 Jul 26.
Severe vitamin D deficiency causes osteomalacia, yet trials of vitamin D supplementation in the community have not on average demonstrated benefit to bone mineral density (BMD) or fracture risk in adults.
To determine whether monthly high-dose vitamin D supplementation influences BMD in the general population and in those with low 25-hydroxyvitamin D levels.
Two-year substudy of a trial in older community-resident adults. A total of 452 participants were randomized to receive monthly doses of vitamin D3 100 000 IU, or placebo. The primary end-point was change in lumbar spine BMD. Exploratory analyses to identify thresholds of baseline 25-hydroxyvitamin D for vitamin D effects on BMD were prespecified.
Intention-to-treat analyses showed no significant treatment effect in the lumbar spine (between-groups difference 0.0071 g cm , 95%CI: -0.0012, 0.0154) or total body but BMD loss at both hip sites was significantly attenuated by ~1/2% over 2 years. There was a significant interaction between baseline 25-hydroxyvitamin D and treatment effect (P = 0.04). With baseline 25-hydroxyvitamin D ≤ 30 nmol L (n = 46), there were between-groups BMD changes at the spine and femoral sites of ~2%, significant in the spine and femoral neck, but there was no effect on total body BMD. When baseline 25-hydroxyvitamin D was >30 nmol L , differences were ~1/2% and significant only at the total hip.
This substudy finds no clinically important benefit to BMD from untargeted vitamin D supplementation of older, community-dwelling adults. Exploratory analyses suggest meaningful benefit in those with baseline 25-hydroxyvitamin D ≤ 30 nmol L . This represents a significant step towards a trial-based definition of vitamin D deficiency for bone health in older adults.
严重的维生素 D 缺乏会导致佝偻病,但社区中维生素 D 补充试验平均并未显示对成年人的骨密度(BMD)或骨折风险有获益。
确定每月大剂量维生素 D 补充是否会影响普通人群和 25-羟维生素 D 水平较低人群的 BMD。
对一项针对老年社区居民的试验进行了为期 2 年的亚研究。共有 452 名参与者被随机分配接受每月 100 000 IU 维生素 D3 或安慰剂。主要终点是腰椎 BMD 的变化。预先指定了探索性分析,以确定基线 25-羟维生素 D 的阈值,以确定维生素 D 对 BMD 的影响。
意向治疗分析显示,腰椎(组间差异 0.0071 g cm ,95%CI:-0.0012,0.0154)或全身 BMD 均无显著治疗效果,但髋部两处的 BMD 丢失在 2 年内显著减少了约 1/2%。基线 25-羟维生素 D 与治疗效果之间存在显著的交互作用(P = 0.04)。当基线 25-羟维生素 D ≤ 30 nmol/L 时(n = 46),脊柱和股骨部位的 BMD 变化有~2%的组间差异,在脊柱和股骨颈处有统计学意义,但对全身 BMD 无影响。当基线 25-羟维生素 D >30 nmol/L 时,差异约为 1/2%,且仅在全髋处有统计学意义。
本亚研究未发现针对普通社区居住的老年人群进行非靶向性维生素 D 补充对 BMD 有临床重要获益。探索性分析表明,基线 25-羟维生素 D ≤ 30 nmol/L 的患者有明显获益。这朝着为老年人骨骼健康基于试验的维生素 D 缺乏定义迈出了重要一步。