Department of Internal Medicine, Division of Endocrinology, Calcium Metabolism and Osteoporosis Program, Beirut, Lebanon.
Scholars in Health Research Program, Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.
J Clin Endocrinol Metab. 2021 Aug 18;106(9):e3644-e3654. doi: 10.1210/clinem/dgab296.
Guidelines for the dosage of vitamin D supplementation vary widely globally.
To investigate the impact of 2 vitamin D doses, bracketed between the IOM recommended dietary allowance (RDA) and the upper tolerable limit, on vitamin D nutritional status in elderly individuals.
This post hoc analysis of data collected from a 12-month, double-blind, randomized control trial included 221 ambulatory participants (≥ 65 years) with a mean BMI of 30.2 kg/m2 and a mean baseline serum 25-hydroxyvitamin D [25(OH)D] level of 20.4 ± 7.4 ng/mL, who were recruited from 3 outpatient centers in Lebanon. All participants received 1000 mg of elemental calcium daily from calcium citrate plus the daily equivalent of either 600 IU or 3750 IU of vitamin D3.
Mean 25(OH)D level at 12 months was 26.0 ng/mL with low dose and 36.0 ng/mL with high dose vitamin D3. The proportion of participants reaching a value ≥ 20 ng/mL was 86% in the low dose, and 99% in the high dose arms, with no gender differences. The increment of 25(OH)D per 100 IU/day was 1 ng/mL with the low dose, and 0.41 ng/mL with the high dose. Serum 25(OH)D levels at 1 year were highly variable in both treatment arms. Baseline 25(OH)D level and vitamin D dose-but not age, BMI, gender, or season-were significant predictors of serum 25(OH)D level post-intervention.
The IOM Recommended Dietary Allowance (RDA) of 600 IU/day does not bring 97.5% of ambulatory elderly individuals above the desirable threshold of 20 ng/mL. Country-specific RDAs are best derived taking into account the observed variability and predictors of achieved 25(OH)D levels.
全球范围内,维生素 D 补充剂量的指南差异很大。
研究 2 种维生素 D 剂量(分别在 IOM 推荐膳食允许量(RDA)和上限耐受量范围内)对老年人维生素 D 营养状况的影响。
本研究是一项为期 12 个月的、双盲、随机对照试验的事后分析,纳入了 221 名有活动能力的参与者(≥65 岁),他们的平均 BMI 为 30.2kg/m2,平均基线血清 25-羟维生素 D [25(OH)D]水平为 20.4±7.4ng/mL,这些参与者是从黎巴嫩的 3 个门诊中心招募的。所有参与者每天服用 1000mg 柠檬酸钙,同时每天摄入相当于 600IU 或 3750IU 的维生素 D3。
低剂量组 12 个月时的平均 25(OH)D 水平为 26.0ng/mL,高剂量组为 36.0ng/mL。低剂量组达到 20ng/mL 以上的参与者比例为 86%,高剂量组为 99%,且无性别差异。低剂量组每增加 100IU/天,25(OH)D 增加 1ng/mL,高剂量组增加 0.41ng/mL。两种治疗组的血清 25(OH)D 水平在 1 年内均高度可变。基线 25(OH)D 水平和维生素 D 剂量-但不是年龄、BMI、性别或季节-是干预后血清 25(OH)D 水平的显著预测因素。
IOM 推荐的膳食允许量(RDA)为 600IU/天,不能使 97.5%的有活动能力的老年人的血清 25(OH)D 水平达到 20ng/mL 以上的理想阈值。最佳的国家特定 RDA 应考虑到观察到的变异性和实现的 25(OH)D 水平的预测因素。