Randomized controlled trial of vitamin D supplementation in older people to optimize bone health

被引:31
作者
Aspray, Terry J. [1 ,2 ]
Chadwick, Thomas [3 ]
Francis, Roger M. [2 ]
McColl, Elaine [3 ]
Stamp, Elaine [3 ]
Prentice, Ann [4 ]
von Wilamowitz-Moellendorff, Alexander [3 ]
Schoenmakers, Inez [4 ,5 ]
机构
[1] NIHR Newcastle Biomed Res Ctr, Campus Aging & Vital, Newcastle Upon Tyne, Tyne & Wear, England
[2] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
[3] Newcastle Univ, Inst Hlth & Soc, Newcastle Upon Tyne, Tyne & Wear, England
[4] MRC Elsie Widdowson Lab, Cambridge, England
[5] Norwich Med Sch, Norwich, Norfolk, England
基金
英国医学研究理事会;
关键词
vitamin D; older people; randomized controlled trial; bone mineral density; dual-energy X-ray absorptiometry; AGED; 65; YEARS; 25-HYDROXYVITAMIN D; DOUBLE-BLIND; PRIMARY HYPERPARATHYROIDISM; FRACTURE PREVENTION; FALLS; DENSITY; METAANALYSIS; COMMUNITY; WOMEN;
D O I
10.1093/ajcn/nqy280
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Vitamin D insufficiency is common in older people and may lead to increased bone resorption, bone loss, and increased falls and fractures. However, clinical trials assessing the effect of vitamin D supplementation on bone mineral density (BMD) have yielded conflicting results. Objectives: This study examined the effect of vitamin D supplementation on BMD at the hip, using dual-energy X-ray absorptiometry. Methods: A total of 379 adults aged >= 70 y (48% women; mean age: 75 y) from the northeast of England were randomly allocated to 1 of 3 doses of vitamin D3 [12,000 international units (IU), 24,000 IU, or 48,000 IU] given once a month. The primary outcome was change in BMD (Delta BMD) at the hip. Secondary endpoints comprised the dose effects on femoral neck BMD, falls, circulating calciotropic hormones, bone turnover markers, and adverse events. Results: The mean +/- SD baseline plasma 25-hydroxyvitamin D [25(OH) D] concentration was 40.0 +/- 20.1 nmol/L, which increased after 12 mo to a mean 25(OH)D of 55.9, 64.6, or 79.0 nmol/L for participants receiving a monthly dose of 12,000, 24,000, or 48,000 IU, respectively (P < 0.01 for difference). There was no between-group difference in Delta BMD. However, parathyroid hormone concentrations decreased in all 3 groups, with a significantly greater decrease in the 48,000-IU group compared with the 12,000-IU group (P < 0.01). There were no differences in any adverse events between groups, with 3 cases of hypercalcemia, none of nephrolithiasis, and 249 falls observed. Conclusions: There was no difference in change in BMD over 12 mo between the 3 doses of vitamin D, suggesting no effect of the intervention or a similar attenuation of the anticipated decrease in BMD over 12 mo. The treatment was safe and effective in increasing plasma 25(OH) D concentrations, with no dose-related adverse events. This trial was registered at the EU Clinical Trials Register (EudraCT 2011-004890-10) and the ISRCTN Registry (ISRCTN35648481).
引用
收藏
页码:207 / 217
页数:11
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