Sleep Medicine Research Group, Sleep Medicine and Research Center, College of Medicine, King Abdulaziz University Hospital, P.O. Box 21589, Jeddah, 80215, Saudi Arabia.
Family and Community Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Sleep Breath. 2019 Jun;23(2):595-601. doi: 10.1007/s11325-018-1751-2. Epub 2018 Nov 14.
Restless legs syndrome is a movement sleep disorder that may be linked to dopaminergic dysfunction and in which vitamin D may play a role. This 12-week randomized, placebo-controlled trial elucidated the efficacy of vitamin D supplements in decreasing restless legs syndrome symptom severity.
Thirty-five subjects with restless legs syndrome, diagnosed using the International Restless Legs Syndrome Study Group criteria, were enrolled. The subjects were randomized to orally receive either vitamin D (50,000 IU caplets) or a placebo. All medications were administered weekly using a direct observation technique. Clinical assessments, including those for restless legs syndrome severity, were conducted at baseline and the end of the study using the International Restless Legs Syndrome Study Group rating scale. The serum vitamin D levels and bone profiles were measured at baseline and every 4 weeks. The primary endpoint was the change in the restless legs syndrome severity score from baseline to week 12. There were 17 and 18 patients in the vitamin D and placebo groups, respectively.
The groups did not differ with respect to age, sex, restless legs syndrome severity, or vitamin D levels. Participants in the vitamin D group showed no significant change in the mean restless legs syndrome severity score compared with the placebo group.
The results suggest that vitamin D supplementation does not improve restless legs syndrome symptoms.
ClinicalTrials.gov : NCT02256215 (available from: https://clinicaltrials.gov/ct2/show/NCT02256215 ).
不宁腿综合征是一种与多巴胺能功能障碍有关的睡眠运动障碍,而维生素 D 可能在此过程中发挥作用。本 12 周随机、安慰剂对照试验旨在阐明补充维生素 D 对降低不宁腿综合征症状严重程度的疗效。
35 例不宁腿综合征患者(根据国际不宁腿综合征研究组标准诊断)纳入本研究。患者被随机分为口服维生素 D(50000IU 胶囊)或安慰剂组。所有药物均采用直接观察技术每周给药一次。临床评估,包括不宁腿综合征严重程度评估,于基线和研究结束时采用国际不宁腿综合征研究组评定量表进行。于基线和每 4 周测量血清维生素 D 水平和骨代谢指标。主要终点为从基线到第 12 周不宁腿综合征严重程度评分的变化。维生素 D 组和安慰剂组分别有 17 例和 18 例患者。
两组在年龄、性别、不宁腿综合征严重程度或维生素 D 水平方面无差异。与安慰剂组相比,维生素 D 组的平均不宁腿综合征严重程度评分无显著变化。
结果表明,维生素 D 补充并不能改善不宁腿综合征的症状。
ClinicalTrials.gov:NCT02256215(可从 https://clinicaltrials.gov/ct2/show/NCT02256215 获得)。