Tuukkanen J, Koivukangas A, Jämsä T, Sundquist K, Mackay C A, Marks S C
Department of Anatomy and Cell Biology, University of Oulu, Finland.
J Bone Miner Res. 2000 Oct;15(10):1905-11. doi: 10.1359/jbmr.2000.15.10.1905.
Bone mineral density (BMD) and mechanical strength generally show strong positive correlations. However, osteopetrosis is a metabolic bone disease with increased skeletal density radiographically and increased risk of fracture. We have evaluated mechanical strength and mineral density in three osteopetrotic mutations in the rat (incisors-absent [ia/ia], osteopetrosis [op/op], and toothless [tl/tl]) to test the hypothesis that reduced bone resorption in one or more of these mutations results in weaker bones in the presence of greater mineral density and skeletal mass. Peripheral quantitative computed tomography (pQCT) was used to analyze BMD and cross-sectional geometry in the tibial diaphysis and metaphysis as well as the femoral diaphysis and femoral neck. The bending breaking force of tibial and femoral midshafts was obtained using the three-point bending test and femoral neck strength was tested by axial loading. Osteopetrotic mutants were significantly smaller than their normal littermates (NLMs) in each stock. The pQCT analysis showed that BMD and bone mineral content (BMC) were higher than or equal to NLMs in all skeletal sites measured in the osteopetrotic mutants. However, the mechanical breaking force was equal to or lower than their NLMs in all sites. The cross-sectional structure of long bone shafts was markedly different in osteopetrotic mutants, having a thin cortex and a medullary area filled with primary trabecular bone. These results indicate that osteopetrotic mutations in the rat increase bone density and decrease bone strength. The tibial diaphysis was significantly weaker in tl/tl and ia/ia mutants and the tibial metaphysis showed the greatest increase in BMD in all mutants. These data are another illustration that an increased BMD does not necessarily lead to stronger bones.
骨密度(BMD)与机械强度通常呈现出强正相关。然而,骨硬化症是一种代谢性骨病,其影像学显示骨骼密度增加且骨折风险升高。我们评估了大鼠三种骨硬化症突变体(无切牙[ia/ia]、骨硬化症[op/op]和无牙[tl/tl])的机械强度和矿物质密度,以检验以下假设:这些突变体中一个或多个的骨吸收减少会导致在矿物质密度和骨骼质量更高的情况下骨骼更脆弱。使用外周定量计算机断层扫描(pQCT)分析胫骨骨干和干骺端以及股骨干和股骨颈的骨密度和横截面几何形状。通过三点弯曲试验获得胫骨和股骨干中部的弯曲断裂力,并通过轴向加载测试股骨颈强度。每个品系的骨硬化症突变体明显小于其正常同窝仔鼠(NLMs)。pQCT分析表明,在骨硬化症突变体测量的所有骨骼部位,骨密度和骨矿物质含量(BMC)高于或等于NLMs。然而,在所有部位,机械断裂力等于或低于其NLMs。骨硬化症突变体长骨骨干的横截面结构明显不同,皮质薄,髓腔区域充满初级小梁骨。这些结果表明,大鼠的骨硬化症突变会增加骨密度并降低骨强度。tl/tl和ia/ia突变体的胫骨干明显更脆弱,并且在所有突变体中,胫骨干骺端的骨密度增加最大。这些数据再次表明,骨密度增加不一定会导致骨骼更强壮。