Farley S M, Libanati C R, Mariano-Menez M R, Tudtud-Hans L A, Schulz E E, Baylink D J
Department of Medicine, Loma Linda University, CA.
J Bone Miner Res. 1990 Mar;5 Suppl 1:S37-42. doi: 10.1002/jbmr.5650051350.
Since osteoporosis is a disease of diminished bone density, and since osteoporotic fractures occur most commonly in the spine, the ideal therapeutic agent for osteoporosis is one which can increase spinal bone density and thereby reduce the risk for vertebral fractures. In the current study we sought to examine the effect of fluoride therapy on spinal bone density utilizing quantitative computed tomography to measure changes in vertebral trabecular bone density during treatment with fluoride. A group of 61 postmenopausal osteoporotic females, aged 70 +/- 9 years, were treated with 34 +/- 7 mg elemental fluoride/day (equivalent to 75 +/- 15 mg NaF/day) and 1500 mg calcium/day for 19 +/- 6 months. Spinal bone density was increased within the first 6 months of fluoride therapy by 42% or 10 +/- 13 mg/cm3 (p less than 0.001) and continued to increased throughout 2 years of observation. The skeletal response to fluoride therapy was also associated with an early increase in serum alkaline phosphatase activity (p less than 0.001), which was related to the increase in spinal bone density (r = .58, p less than 0.001). Large interpatient variation was observed in the spinal bone response to fluoride therapy, which was not explained by variations in the pretreatment spinal bone density (r = .04), age of the patient (r = .15), or dose of fluoride (r = .16). Results from these studies demonstrate (1) the therapeutic value of fluoride to increase trabecular bone density linearly for 2 years in the osteoporotic spine and (2) the clinical value of measuring spinal bone density and/or serum alkaline phosphatase activity as indices of the skeletal response to fluoride.
由于骨质疏松症是一种骨密度降低的疾病,且骨质疏松性骨折最常发生在脊柱,因此治疗骨质疏松症的理想药物是一种能够增加脊柱骨密度从而降低椎体骨折风险的药物。在本研究中,我们试图利用定量计算机断层扫描来检测氟化物治疗对脊柱骨密度的影响,以测量氟化物治疗期间椎骨小梁骨密度的变化。一组61名绝经后骨质疏松女性,年龄70±9岁,接受每日34±7毫克元素氟(相当于每日75±15毫克氟化钠)和1500毫克钙的治疗,为期19±6个月。在氟化物治疗的前6个月内,脊柱骨密度增加了42%或10±13毫克/立方厘米(p<0.001),并在整个2年的观察期内持续增加。氟化物治疗的骨骼反应还与血清碱性磷酸酶活性的早期增加有关(p<0.001),这与脊柱骨密度的增加相关(r = 0.58,p<0.001)。观察到患者对氟化物治疗的脊柱骨反应存在较大个体差异,这无法用治疗前脊柱骨密度的差异(r = 0.04)、患者年龄(r = 0.15)或氟化物剂量(r = 0.16)来解释。这些研究结果表明:(1)氟化物对骨质疏松脊柱的小梁骨密度有持续2年的线性增加的治疗价值;(2)测量脊柱骨密度和/或血清碱性磷酸酶活性作为对氟化物骨骼反应指标的临床价值。