Hodsman A B, Drost D J
Department of Medicine, St Joseph's Health Centre, London, Ontario, Canada.
J Clin Endocrinol Metab. 1989 Nov;69(5):932-8. doi: 10.1210/jcem-69-5-932.
Forty-eight female patients with postmenopausal osteoporotic vertebral compression fractures were treated with sodium fluoride and calcium supplements; their response to treatment was documented by sequential measurements of vertebral and forearm bone mineral density (BMD). During treatment 25 patients developed significant side-effects due to fluoride, and ultimately, 18 patients (37%) were intolerant of the drug after 17.3 +/- 7.3 (+/- SD) months. The remaining patients were followed for 29.4 +/- 9.6 months. By linear regression analysis, 69% of patients had a positive slope of vertebral BMD vs. time of greater than 0.0017 g/cm2.month (range, 0.0017-0.01) and were classified as treatment responders. The increment in vertebral BMD above the baseline value over time was described by the relationship delta BMD (g/cm2.month) = 0.042 + 0.0053 x months, equivalent to a rate of 8.4%/yr. Because the rates of increasing BMD were very variable, it was difficult to determine in individual patients the point at which a positive response to treatment had occurred; by calculating the 95% confidence target BMD by which the BMD must rise above the initial value before discounting the imprecision of the measurements (0.062 g/cm2), only 70% of responders were identified by 12 months. The total cumulative dose of sodium fluoride (31.3 +/- 16.4 g) was significantly higher in patients classified as responders than in the nonresponders (20.6 +/- 13.4 g; P less than 0.05), probably because of differences in side-effects between the two groups. In contrast, forearm BMD fell significantly in the responders by an average of 7.7%/yr, suggesting the possibility of a preferential improvement in axial bone density at the expense of cortical bone. Thus, the majority of patients treated with fluoride respond with increasing vertebral BMD, but it may take 12-24 months to identify these individually.
48例绝经后骨质疏松性椎体压缩骨折的女性患者接受了氟化钠和钙剂治疗;通过连续测量椎体和前臂骨密度(BMD)记录她们对治疗的反应。治疗期间,25例患者因氟化物出现明显副作用,最终,18例患者(37%)在17.3±7.3(±标准差)个月后对该药物不耐受。其余患者随访了29.4±9.6个月。通过线性回归分析,69%的患者椎体BMD与时间的正斜率大于0.0017 g/cm²·月(范围为0.0017 - 0.01),被归类为治疗反应者。随着时间推移,椎体BMD相对于基线值的增量由关系ΔBMD(g/cm²·月)= 0.042 + 0.0053×月描述,相当于每年8.4%的增长率。由于BMD增加率变化很大,很难在个体患者中确定对治疗产生阳性反应的时间点;通过计算95%置信目标BMD(在不考虑测量不精确性之前,BMD必须高于初始值的数值为0.062 g/cm²),到12个月时仅识别出70%的反应者。被归类为反应者的患者氟化钠总累积剂量(31.3±16.4 g)显著高于无反应者(20.6±13.4 g;P<0.05),这可能是由于两组副作用不同所致。相比之下,反应者的前臂BMD平均每年显著下降7.7%,提示可能以皮质骨为代价优先改善轴向骨密度。因此,大多数接受氟化物治疗的患者椎体BMD会增加,但可能需要12 - 24个月才能逐个识别出这些患者。