Hui S L, Slemenda C W, Johnston C C
Indiana University School of Medicine.
Ann Intern Med. 1989 Sep 1;111(5):355-61. doi: 10.7326/0003-4819-111-5-355.
To determine if a single bone mass measurement of the radius is predictive of future fractures at any site.
Observational study of a cohort of free-living subjects and a cohort of retirement-home residents with an average follow-up of 6.7 years and 5.5 years, respectively (range, 1 to 15 years for both cohorts).
General community and a retirement home.
Volunteer sample of white women (386 free-living and 135 living in a retirement home) who were free of disease and were not receiving medication known to affect bone metabolism. In terms of physical condition subjects ranged from the totally independent to the wheelchair-bound.
A radial bone mass measurement was done at the initial visit. Subsequent non-spine fractures were reported by the subjects at follow-up visits, which were less than a year apart in most cases, and verified with medical records. Cox regression was used to model time to first fracture as a function of age and bone mass. These analyses showed that for every 0.1 g/cm decrement in bone mass, the relative risk of fracture was 2.2 (CI, 1.7 to 2.8) for the free-living and 1.5 (CI, 1.2 to 1.9) for the retirement-home residents. Baseline age did not predict the risk of fracture in either cohort, and controlling for baseline age did not reduce the relative-risk estimates of bone mass. Similar analyses also showed that bone mass was a statistically significant predictor for first hip fractures (n = 30) among the nursing-home residents (relative risk, 1.9; CI, 1.4 to 2.7) and first forearm fractures (n = 10) among the free living (relative risk, 3.6; CI, 1.9 to 6.8). For both cohorts, the 8-year probability of any nonspine fracture was about 80% for subjects with initial bone mass less than 0.6 g/cm and was less than 10% for subjects with initial bone mass greater than 0.8 g/cm. Similarly, those in the retirement home with bone mass below 0.6 g/cm had a 6-year probability of hip fracture of 43%, compared with a 17% risk for those with greater bone mass.
A single bone mass measurement of the radius is predictive of future nonspine fractures at all sites, and at both the forearm and the hip. Baseline age was not a significant predictor of fracture within either cohort. Relative-risk estimates were not dissimilar across fracture sites.
确定单次桡骨骨量测量能否预测未来任何部位的骨折。
对一组自由生活的受试者和一组养老院居民进行观察性研究,平均随访时间分别为6.7年和5.5年(两组的随访时间范围均为1至15年)。
普通社区和一家养老院。
白人女性志愿者样本(386名自由生活者和135名居住在养老院者),她们无疾病且未服用已知会影响骨代谢的药物。就身体状况而言,受试者范围从完全独立到需要轮椅辅助。
在初次就诊时进行桡骨骨量测量。受试者在随访时报告了随后发生的非脊柱骨折情况,大多数情况下随访间隔不到一年,并通过医疗记录进行核实。采用Cox回归模型将首次骨折时间作为年龄和骨量的函数。这些分析表明,对于自由生活的受试者,骨量每减少0.1 g/cm,骨折的相对风险为2.2(置信区间为1.7至2.8);对于养老院居民,该风险为1.5(置信区间为1.2至1.9)。基线年龄在两组中均不能预测骨折风险,且控制基线年龄并不能降低骨量的相对风险估计值。类似分析还表明,骨量对于养老院居民中的首次髋部骨折(n = 30)(相对风险为1.9;置信区间为1.4至2.7)和自由生活者中的首次前臂骨折(n = 10)(相对风险为3.6;置信区间为1.9至6.8)具有统计学意义的预测作用。对于两组受试者,初始骨量小于0.6 g/cm的人发生任何非脊柱骨折的8年概率约为80%,而初始骨量大于0.8 g/cm的人该概率小于10%。同样,养老院中骨量低于0.6 g/cm的人髋部骨折的6年概率为43%,而骨量较高者的风险为17%。
单次桡骨骨量测量可预测未来所有部位以及前臂和髋部的非脊柱骨折。基线年龄在两组中均不是骨折的显著预测因素。不同骨折部位的相对风险估计值并无差异。