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氟化物治疗骨质疏松症:周期性非盲法研究还是连续性盲法研究?

Fluoride treatment of osteoporosis: cyclical non-blinded or continuous blinded studies?

作者信息

Gutteridge D H, Kent G N, Prince R L, Nicholson G C, Stewart G O, Jones C E, Bhagat C I, Stuckey B G, Retallack R W

机构信息

Department of Endocrinology/Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia.

出版信息

Osteoporos Int. 1993;3 Suppl 1:215-7. doi: 10.1007/BF01621911.

Abstract

The future of sodium fluoride (NaF), the most potent osteoblast stimulator known to man, is in the balance. Of three recent randomized trials of continuous NaF only one found a significant in vertebral fractures in the NaF group. When data from the first year were excluded, two of the studies (those with the largest numbers) showed a significantly reduced risk of vertebral fracture on NaF. The effect of NaF on cortical bone is poorly documented. Two studies have shown reduced forearm cortical bone density with continuous NaF. A further two (histomorphometric) studies have shown the development of increased cortical porosity on continuous NaF treatment. In one, this was selectively at the external cortex and was linearly correlated with cancellous volume increase. Our pilot study using NaF administered cyclically has shown an encouraging (though non-significant) reduction in vertebral fracture rates (excluding year 1) and no fall in forearm cortical density. Another (US) cyclical study has shown no increase in cortical porosity. A current W. Australian randomized study of 50 patients is described where NaF dosage is varied proportional to the osteoblast response, and duration is dependent on densitometric and radiographic response. The future of NaF should involve cyclical administration, in cautious initial dosage (50-60 mg/day) of enteric-coated NaF, in conjunction with a potent inhibitor of resorption such as hormone replacement, bisphosphonates or calcitonin.

摘要

氟化钠(NaF),人类已知最有效的成骨细胞刺激剂,其未来尚不明朗。在最近三项关于持续使用NaF的随机试验中,只有一项发现NaF组椎体骨折有显著差异。若排除第一年的数据,其中两项研究(样本量最大的两项)显示,使用NaF可显著降低椎体骨折风险。关于NaF对皮质骨的影响,相关文献记载较少。两项研究表明,持续使用NaF会降低前臂皮质骨密度。另有两项(组织形态计量学)研究显示,持续使用NaF治疗会使皮质骨孔隙率增加。其中一项研究表明,这种情况在外侧皮质有选择性地出现,且与松质骨体积增加呈线性相关。我们使用周期性给药NaF的初步研究显示,椎体骨折率有令人鼓舞的降低(不包括第一年)且前臂皮质骨密度没有下降(尽管差异不显著)。另一项(美国的)周期性研究显示皮质骨孔隙率没有增加。本文描述了西澳大利亚目前一项针对50名患者的随机研究,其中NaF剂量根据成骨细胞反应成比例变化,治疗持续时间取决于骨密度测定和影像学反应。NaF的未来应用应采用周期性给药,初始谨慎剂量为肠溶包衣NaF 50 - 60毫克/天,并结合一种有效的骨吸收抑制剂,如激素替代疗法、双膦酸盐或降钙素。

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