Hin H, Tomson J, Newman C, Kurien R, Lay M, Cox J, Sayer J, Hill M, Emberson J, Armitage J, Clarke R
Hightown Surgery, Banbury, Oxfordshire, UK.
Clinical Trial Service Unit (CTSU) and Epidemiological Studies Unit and MRC Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Osteoporos Int. 2017 Mar;28(3):841-851. doi: 10.1007/s00198-016-3833-y. Epub 2016 Dec 16.
This trial compared the effects of daily treatment with vitamin D or placebo for 1 year on blood tests of vitamin D status. The results demonstrated that daily 4000 IU vitamin D3 is required to achieve blood levels associated with lowest disease risks, and this dose should be tested in future trials for fracture prevention.
The aim of this trial was to assess the effects of daily supplementation with vitamin D3 4000 IU (100 μg), 2000 IU (50 μg) or placebo for 1 year on biochemical markers of vitamin D status in preparation for a large trial for prevention of fractures and other outcomes.
This is a randomized placebo-controlled trial in 305 community-dwelling people aged 65 years or older in Oxfordshire, UK. Outcomes included biochemical markers of vitamin D status (plasma 25-hydroxy-vitamin D [25[OH]D], parathyroid hormone [PTH], calcium and alkaline phosphatase), cardiovascular risk factors and tests of physical function.
Mean (SD) plasma 25(OH)D levels were 50 (18) nmol/L at baseline and increased to 137 (39), 102 (25) and 53 (16) nmol/L after 12 months in those allocated 4000 IU, 2000 IU or placebo, respectively (with 88%, 70% and 1% of these groups achieving the pre-specified level of >90 nmol/L). Neither dose of vitamin D3 was associated with significant deviation outside the normal range of PTH or albumin-corrected calcium. The additional effect on 25(OH)D levels of 4000 versus 2000 IU was similar in all subgroups except for body mass index, for which the further increase was smaller in overweight and obese participants compared with normal-weight participants. Supplementation with vitamin D had no significant effects on cardiovascular risk factors or on measures of physical function.
After accounting for average 70% compliance in long-term trials, doses of 4000 IU vitamin D3 daily may be required to achieve plasma 25(OH)D levels associated with lowest disease risk in observational studies.
本试验比较了每日服用维生素D或安慰剂1年对维生素D状态血液检测指标的影响。结果表明,每日需要4000国际单位维生素D3才能达到与最低疾病风险相关的血液水平,该剂量应在未来预防骨折的试验中进行测试。
本试验的目的是评估每日补充4000国际单位(100微克)、2000国际单位(50微克)维生素D3或安慰剂1年对维生素D状态生化指标的影响,为一项预防骨折及其他结局的大型试验做准备。
这是一项在英国牛津郡305名65岁及以上社区居民中进行的随机安慰剂对照试验。结局指标包括维生素D状态的生化指标(血浆25-羟基维生素D [25(OH)D]、甲状旁腺激素 [PTH]、钙和碱性磷酸酶)、心血管危险因素和身体功能测试。
基线时平均(标准差)血浆25(OH)D水平为50(18)纳摩尔/升,在分配接受4000国际单位、2000国际单位或安慰剂治疗12个月后,分别升至137(39)、102(25)和53(16)纳摩尔/升(这些组中分别有88%、70%和1%达到预先设定的>90纳摩尔/升水平)。两种剂量的维生素D3均未导致PTH或白蛋白校正钙超出正常范围的显著偏差。除体重指数外,在所有亚组中,4000国际单位与2000国际单位对25(OH)D水平的额外影响相似,与正常体重参与者相比,超重和肥胖参与者中进一步升高的幅度较小。补充维生素D对心血管危险因素或身体功能指标无显著影响。
考虑到长期试验中平均70%的依从性,每日可能需要4000国际单位维生素D3才能在观察性研究中达到与最低疾病风险相关的血浆25(OH)D水平。