Lems W F, Jacobs W G, Bijlsma J W, Croone A, Haanen H C, Houben H H, Gerrits M I, van Rijn H J
Department of Rheumatology and Clinical Immunology, Utrecht University Hospital, The Netherlands.
Osteoporos Int. 1997;7(6):575-82. doi: 10.1007/BF02652565.
To investigate whether sodium fluoride (NaF) is able to prevent bone loss in patients treated with corticosteroids (Cs), we performed a randomized double-masked, placebo-controlled trial with 44 Cs-treated patients without established osteoporosis, defined as the absence of previous peripheral fractures and vertebral deformities on radiographs. The effects of NaF (25 mg twice daily) and placebo on the bone mineral density (BMD) of the lumbar spine and hips were compared at baseline and at 6, 12, 18 and 24 months. After 2 years, the BMD of the lumbar spine had decreased in the placebo group by 3.0% (95% CI: -4.9% to -1.0%; p < 0.01); in the NaF group there was a statistically insignificant increase in BMD of 2.2% (95% CI: -0.8% to +5.3%). The difference in the changes in BMD between the two groups was +5.2% (95% CI: +1.8% to +8.6%; p < 0.01). In the hips, BMD had decreased after 2 years in both groups: in the placebo group by -3.0% (95% CI: -5.0% to -1.0%; p < 0.05) and in the NaF group by 3.8% (95% CI: -6.1% to -1.5%; p < 0.01). The difference in the changes in BMD between the two groups was not significant: +0.8% (95% CI: -2.1% to +3.8%). Three vertebral deformities were observed in the placebo group and one in the NaF group (insignificant difference), while no peripheral fractures occurred during the study period. It is concluded that in Cs-treated patients without established osteoporosis NaF prevents bone loss in the lumbar spine but does not have a positive effect on the BMD of the hips.
为了研究氟化钠(NaF)是否能够预防接受皮质类固醇(Cs)治疗患者的骨质流失,我们对44名未患骨质疏松症的Cs治疗患者进行了一项随机双盲、安慰剂对照试验,骨质疏松症的定义为既往无外周骨折且X线片上无椎体畸形。在基线以及6、12、18和24个月时,比较了NaF(每日两次,每次25mg)和安慰剂对腰椎和髋部骨密度(BMD)的影响。2年后,安慰剂组腰椎骨密度下降了3.0%(95%CI:-4.9%至-1.0%;p<0.01);NaF组骨密度有统计学意义的增加,为2.2%(95%CI:-0.8%至+5.3%)。两组骨密度变化的差异为+5.2%(95%CI:+1.8%至+8.6%;p<0.01)。在髋部,两组2年后骨密度均下降:安慰剂组下降-3.0%(95%CI:-5.0%至-1.0%;p<0.05),NaF组下降3.8%(95%CI:-6.1%至-1.5%;p<0.01)。两组骨密度变化的差异不显著:+0.8%(95%CI:-2.1%至+3.8%)。安慰剂组观察到3例椎体畸形,NaF组观察到1例(差异不显著),而研究期间未发生外周骨折。得出的结论是,在未患骨质疏松症的Cs治疗患者中,NaF可预防腰椎骨质流失,但对髋部骨密度没有积极影响。