Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Department of Endocrinology and Diabetes, Royal Brisbane and Women's Hospital, Brisbane, Australia.
J Cachexia Sarcopenia Muscle. 2021 Dec;12(6):1428-1439. doi: 10.1002/jcsm.12759. Epub 2021 Aug 1.
Falls cause considerable morbidity and mortality in older people. It is unclear how vitamin D supplementation affects falls risk, particularly when taken at high doses. We sought to determine whether monthly high-dose vitamin D supplementation reduces risk and incidence of falls.
We used data from the randomized, double-blind, placebo-controlled D-Health Trial conducted in Australia. Between February 2014 and May 2015, 21 315 participants aged 60-84 years were randomized (1:1) to monthly doses of either 60 000 IU of colecalciferol or placebo for a maximum of 5 years. People who reported a history of osteomalacia, sarcoidosis, hyperparathyroidism, hypercalcaemia or kidney stones or who were taking >500 IU/day supplementary vitamin D were ineligible. Each year, we collected blood samples from ~450 randomly sampled participants from each trial arm and measured 25-hydroxyvitamin D [25(OH)D]. Falls, a prespecified tertiary outcome, were ascertained using annual surveys and, for a subset of participants, 3-month falls diaries. The primary outcome for this analysis was any fall in the month before completing an annual survey. As part of our process to maintain blinding, we used random samples of participants (surveys, n = 16 000; diaries, n = 2400), with equal numbers per group. Participants with no outcome data were excluded. Following an intention-to-treat approach, we analysed outcomes using logistic, ordinal and negative binomial regression. Registration: Australian New Zealand Clinical Trials Registry (ACTRN12613000743763); registered 4 July 2013.
Mean treatment duration was 4.3 years (standard deviation [SD] = 1.4 years). Mean serum 25(OH)D concentrations during the trial were 114.8 (SD 30.3) nmol/L and 77.5 (SD 25.2) nmol/L in the vitamin D and placebo groups, respectively. Survey and diary analytic sets included 15 416 and 2200 participants, respectively; approximately half were randomized to vitamin D (surveys: 50.1%; diaries: 50.4%). Vitamin D had no effect on falling in the past month (odds ratio [OR] 1.02, 95% confidence interval [CI] 0.95-1.10). There was an interaction with body mass index (BMI) (P-interaction = 0.001); vitamin D increased risk in participants with BMI < 25 kg/m (OR 1.25, 95% CI 1.09-1.43), but there was no effect in those with BMI ≥ 25 kg/m (OR 0.95, 95% CI 0.87-1.04). Analyses of diary data were consistent with these findings. The incidence of hypercalcaemia and kidney stones did not differ between groups.
Monthly high-dose vitamin D supplementation did not reduce risk of falling. A possible increased risk of falling with vitamin D supplementation in people with normal BMI warrants further investigation.
老年人跌倒会导致相当大的发病率和死亡率。目前尚不清楚维生素 D 补充剂如何影响跌倒风险,特别是当剂量较高时。我们旨在确定每月高剂量维生素 D 补充剂是否可以降低跌倒风险和发生率。
我们使用了在澳大利亚进行的随机、双盲、安慰剂对照 D-Health 试验的数据。2014 年 2 月至 2015 年 5 月,将 21315 名 60-84 岁的参与者随机(1:1)分为每月服用 60000 IU 胆钙化醇或安慰剂组,最长 5 年。有佝偻病、结节病、甲状旁腺功能亢进、高钙血症或肾结石病史或正在服用>500IU/天补充维生素 D 的人不符合条件。每年,我们从每个试验臂中随机抽取约 450 名参与者收集血液样本,并测量 25-羟基维生素 D[25(OH)D]。跌倒,作为预先指定的三级结局,通过年度调查和对一部分参与者的 3 个月跌倒日记进行确定。本次分析的主要结局是在完成年度调查前一个月的任何跌倒。作为我们保持盲法的过程的一部分,我们使用了参与者的随机样本(调查,n=16000;日记,n=2400),每组人数相等。没有结局数据的参与者被排除在外。我们采用意向治疗方法,使用逻辑回归、有序和负二项回归分析结局。注册:澳大利亚和新西兰临床试验注册中心(ACTRN12613000743763);2013 年 7 月 4 日注册。
平均治疗持续时间为 4.3 年(标准差[SD] = 1.4 年)。试验期间,血清 25(OH)D 浓度分别为维生素 D 组 114.8(SD 30.3)nmol/L和安慰剂组 77.5(SD 25.2)nmol/L。调查和日记分析集分别包括 15416 名和 2200 名参与者,其中约一半随机分配至维生素 D 组(调查:50.1%;日记:50.4%)。维生素 D 对过去一个月的跌倒没有影响(比值比[OR] 1.02,95%置信区间[CI] 0.95-1.10)。与体重指数(BMI)存在交互作用(P 交互=0.001);在 BMI<25kg/m2 的参与者中,维生素 D 增加了风险(OR 1.25,95%CI 1.09-1.43),但在 BMI≥25kg/m2 的参与者中没有影响(OR 0.95,95%CI 0.87-1.04)。对日记数据的分析与这些发现一致。高钙血症和肾结石的发生率在两组之间没有差异。
每月高剂量维生素 D 补充剂并未降低跌倒风险。在 BMI 正常的人群中,维生素 D 补充剂可能增加跌倒风险,这一发现值得进一步研究。