Lundy M W, Stauffer M, Wergedal J E, Baylink D J, Featherstone J D, Hodgson S F, Riggs B L
Pettis Veterans Hospital, Loma Linda, California, USA.
Osteoporos Int. 1995 Mar;5(2):115-29. doi: 10.1007/BF01623313.
In a 4-year controlled, prospective trial, histomorphometric analysis was used to compare the tissue-level skeletal effects of fluoride therapy in 43 postmenopausal women (75 mg NaF/day) with those of 35 matching placebo subjects; all subjects received 1500 mg/day elemental calcium supplement. In addition to an initial, baseline biopsy, a second biopsy was obtained after 6, 18, 30 or 48 months. Measurements were made on a third biopsy obtained from 8 subjects following at least 72 months of fluoride therapy. The change in cancellous bone volume or trabecular thickness in fluoride-treated subjects was not different from a change in placebo-treated subjects. However, paired analysis in the fluoride-treated subjects indicated that bone volume was increased between the first and second biopsies (p < 0.005). Both osteoid length and width were significantly increased in fluoride compared with placebo subjects; however, only the osteoid surface increased linearly (r = 0.63, p < 0.001). The mineral apposition rate and relative tetracycline-covered bone surface were not different between fluoride and placebo treatment, although they were decreased in both groups in the second biopsy. The tetracycline-covered bone surface returned to normal in the third biopsy. Definitive evidence for osteomalacia is a prolonged mineralization lag time, which following fluoride treatment was found to be increased 9-fold in the second biopsy and 4-fold in the third biopsy. Further evidence for osteomalacia was increased osteoid thickness by 6 months, evidence of focal areas of interstitial mineralization defects, and broad tetracycline labels of low fluorescence intensity. In the third biopsies, osteoclastic resorption was observed beneath osteoid seams. Fluoride therapy increased the cortical width compared with placebo treatment (p < 0.02), and increased the osteoid surface in Haversian canals, but did not change the osteoid width, resorption surface or cortical porosity. After an initial rise, serum fluoride levels remained constant, and the urine values fell slightly. The bone fluoride concentration rose throughout the treatment period, and was correlated with the change in osteoid-covered bone surface (r = 0.56, p < 0.001). Although we found definitive evidence for osteomalacia, the cause of the osteomalacia was not determined in this study. On the other hand, the presence of bone resorption beneath unmineralized osteoid and of osteocyte halos is suggestive of hyperparathyroidism. Thus, it is possible that the strong stimulus for bone formation brought about by fluoride therapy resulted in relative calcium deficiency.
在一项为期4年的对照前瞻性试验中,采用组织形态计量学分析方法,比较了43名绝经后妇女(每日服用75毫克氟化钠)接受氟化物治疗与35名匹配的服用安慰剂受试者的组织水平骨骼效应;所有受试者均每日补充1500毫克元素钙。除了进行初始的基线活检外,在6、18、30或48个月后获取第二次活检样本。对8名接受至少72个月氟化物治疗的受试者进行的第三次活检样本进行了测量。接受氟化物治疗的受试者的松质骨体积或小梁厚度变化与接受安慰剂治疗的受试者无差异。然而,对接受氟化物治疗的受试者进行配对分析表明,第一次和第二次活检之间骨体积增加(p < 0.005)。与安慰剂组受试者相比,氟化物组的类骨质长度和宽度均显著增加;然而,只有类骨质表面呈线性增加(r = 0.63,p < 0.001)。氟化物治疗组和安慰剂治疗组之间的矿物质沉积率和四环素覆盖的骨表面无差异,尽管两组在第二次活检时均有所下降。第三次活检时,四环素覆盖的骨表面恢复正常。骨软化症的确切证据是矿化延迟时间延长,氟化物治疗后,第二次活检时矿化延迟时间增加了9倍,第三次活检时增加了4倍。骨软化症的进一步证据包括6个月时类骨质厚度增加、间质矿化缺陷局部区域的证据以及低荧光强度的宽四环素标记。在第三次活检中,在类骨质缝下方观察到破骨细胞吸收。与安慰剂治疗相比,氟化物治疗增加了皮质宽度(p < 0.02),并增加了哈弗斯管内的类骨质表面,但未改变类骨质宽度、吸收表面或皮质孔隙率。血清氟化物水平在最初升高后保持稳定,尿液值略有下降。整个治疗期间骨氟浓度升高,并与类骨质覆盖的骨表面变化相关(r = 0.56,p < 0.001)。尽管我们发现了骨软化症的确切证据,但本研究未确定骨软化症的病因。另一方面,未矿化类骨质下方存在骨吸收和骨细胞晕提示甲状旁腺功能亢进。因此,有可能氟化物治疗引起的强烈骨形成刺激导致了相对钙缺乏。