Rahme Maya, Sharara Sima Lynn, Baddoura Rafic, Habib Robert H, Halaby Georges, Arabi Asma, Singh Ravinder J, Kassem Moustapha, Mahfoud Ziyad, Hoteit Maha, Daher Rose T, Bassil Darina, El Ferkh Karim, El-Hajj Fuleihan Ghada
Department of Internal Medicine, Division of Endocrinology, Calcium Metabolism and Osteoporosis Program, WHO Collaborating Center for Metabolic Bone Disorders, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Rheumatology, Hotel Dieu de France, Beirut, Lebanon.
J Bone Miner Res. 2017 Jul;32(7):1486-1495. doi: 10.1002/jbmr.3122. Epub 2017 May 18.
The optimal dose of vitamin D to optimize bone metabolism in the elderly is unclear. We tested the hypothesis that vitamin D, at a dose higher than recommended by the Institute of Medicine (IOM), has a beneficial effect on bone remodeling and mass. In this double-blind trial we randomized 257 overweight elderly subjects to receive 1000 mg of elemental calcium citrate/day, and the daily equivalent of 3750 IU/day or 600 IU/day of vitamin D3 for 1 year. The subjects' mean age was 71 ± 4 years, body mass index 30 ± 4 kg/m , 55% were women, and 222 completed the 12-month follow-up. Mean serum 25 hydroxyvitamin D (25OHD) was 20 ng/mL, and rose to 26 ng/mL in the low-dose arm, and 36 ng/mL in the high-dose arm, at 1 year (p < 0.05). Plasma parathyroid hormone, osteocalcin, and C-terminal telopeptide (Cross Laps) levels decreased significantly by 20% to 22% in both arms, but there were no differences between the two groups for any variable, at 6 or 12 months, with the exception of serum calcitriol, which was higher in the high-dose group at 12 months. Bone mineral density (BMD) increased significantly at the total hip and lumbar spine, but not the femoral neck, in both study arms, whereas subtotal body BMD increased in the high-dose group only, at 1 year. However, there were no significant differences in percent change BMD between the two study arms at any skeletal site. Subjects with serum 25OHD <20 ng/mL and PTH level >76 pg/mL showed a trend for higher BMD increments at all skeletal sites, in the high-dose group, that reached significance at the hip. Adverse events were comparable in the two study arms. This controlled trial shows little additional benefit in vitamin D supplementation at a dose exceeding the IOM recommendation of 600 IU/day on BMD and bone markers, in overweight elderly individuals. © 2017 American Society for Bone and Mineral Research.
目前尚不清楚用于优化老年人骨骼代谢的维生素D最佳剂量。我们检验了这样一个假设:剂量高于美国医学研究所(IOM)推荐量的维生素D对骨重塑和骨量具有有益作用。在这项双盲试验中,我们将257名超重老年人随机分为两组,一组每天服用1000毫克枸橼酸钙元素,以及相当于每日3750国际单位或600国际单位的维生素D3,为期1年。受试者的平均年龄为71±4岁,体重指数为30±4kg/m²,55%为女性,222人完成了12个月的随访。平均血清25羟维生素D(25OHD)水平为20ng/mL,1年后低剂量组升至26ng/mL,高剂量组升至36ng/mL(p<0.05)。两组血浆甲状旁腺激素、骨钙素和C末端肽(Cross Laps)水平均显著下降20%至22%,但在6个月或12个月时,除血清骨化三醇在12个月时高剂量组较高外,两组在任何变量上均无差异。两个研究组的全髋和腰椎骨密度均显著增加,但股骨颈骨密度未增加,而仅高剂量组的全身骨密度在1年时增加。然而,两个研究组在任何骨骼部位的骨密度变化百分比均无显著差异。血清25OHD<20ng/mL且甲状旁腺激素水平>76pg/mL的受试者在高剂量组中所有骨骼部位的骨密度增加趋势更高,在髋部达到显著水平。两个研究组的不良事件相当。这项对照试验表明,对于超重老年人,剂量超过IOM推荐的600国际单位/天补充维生素D对骨密度和骨标志物几乎没有额外益处。©2017美国骨与矿物质研究学会。