Bleicher Kerrin, Cumming Robert G, Naganathan Vasikaran, Blyth Fiona M, Le Couteur David G, Handelsman David J, Waite Louise M, Seibel Markus J
School of Public Health, University of Sydney, Sydney, Australia.
J Bone Miner Res. 2014 Sep;29(9):2024-31. doi: 10.1002/jbmr.2230.
The aim of this population-based, prospective, observational study was to examine the relationship between serum levels of 25-hydroxyvitamin D (25OHD) and fracture risk in a cohort of 1662 community-dwelling men aged 70 to 97 years followed for a mean of 4.3 years. Data about mobility, muscle strength, balance, medication use, cognition, medical history, lifestyle factors, renal function, and serum 25OHD were collected at baseline. Data on radiologically verified fractures were collected every 4 months. The relationship between fractures and serum 25OHD levels was analyzed using Cox's proportional hazard regression. We accounted for bone mineral density, falls, physical activity, sun exposure, and season of blood draw, in addition to anthropometric and lifestyle factors, medical history, muscle strength, balance, and medication and supplement use. There were 123 first-incident fragility fractures. The relationship between baseline 25OHD and fracture risk was U-shaped, with increased fracture risk in men with either low or high serum 25OHD levels. In multivariate analysis, the risk of fracture was greatest in men with 25OHD levels in the lowest quintile (25OHD ≤36 nmol/L; hazard ratio [HR] = 3.5; 95% confidence interval [CI] 1.7-7.0) and in men in the highest quintile (25OHD >72 nmol/L; HR = 2.7; 95% CI 1.4-5.4) compared with men in the 4th quintile (25OHD ≥60 to ≤72 nmol/L). These associations were not explained by lower BMD, increased physical activity, fall risk, or other lifestyle or anthropomorphic factors. In community-dwelling older men, there appears to be a healthy target range for serum 25OHD concentrations. Thus, serum 25OHD levels too high and too low may be harmful in regard to fracture risk.
这项基于人群的前瞻性观察性研究旨在调查1662名年龄在70至97岁之间的社区居住男性队列中,血清25-羟基维生素D(25OHD)水平与骨折风险之间的关系,这些男性平均随访了4.3年。在基线时收集了有关活动能力、肌肉力量、平衡能力、药物使用、认知、病史、生活方式因素、肾功能和血清25OHD的数据。每4个月收集一次经放射学证实的骨折数据。使用Cox比例风险回归分析骨折与血清25OHD水平之间的关系。除了人体测量和生活方式因素、病史、肌肉力量、平衡能力以及药物和补充剂使用情况外,我们还考虑了骨密度、跌倒、身体活动、阳光暴露和采血季节。共有123例首次发生的脆性骨折。基线25OHD与骨折风险之间的关系呈U形,血清25OHD水平过低或过高的男性骨折风险增加。在多变量分析中,与处于第4个五分位数(25OHD≥60至≤72 nmol/L)的男性相比,25OHD水平处于最低五分位数(25OHD≤36 nmol/L;风险比[HR]=3.5;95%置信区间[CI] 1.7-7.0)和最高五分位数(25OHD>72 nmol/L;HR=2.7;95%CI 1.4-5.4)的男性骨折风险最高。这些关联不能用较低的骨密度、增加的身体活动、跌倒风险或其他生活方式或人体形态学因素来解释。在社区居住的老年男性中,血清25OHD浓度似乎存在一个健康的目标范围。因此,血清25OHD水平过高和过低在骨折风险方面可能都是有害的。