Contribution of the intra-specimen variations in tissue mineralization to PTH- and raloxifene-induced changes in stiffness of rat vertebrae

被引:29
作者
Easley, Sarah K. [1 ]
Jekir, Michael G. [1 ]
Burghardt, Andrew J. [2 ]
Li, Mei [3 ]
Keaveny, Tony M. [1 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Mech Engn, Orthopaed Biomech Lab, Berkeley, CA 94720 USA
[2] Univ Calif San Francisco, Musculoskeletal & Quantitat Imaging Res Grp, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA
[3] Pfizer Inc, Groton, CT 06340 USA
[4] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
关键词
Bone mineralization; Finite element analysis; Bone biomechanics; Raloxifene; PTH; MECHANICAL-PROPERTIES; PARATHYROID-HORMONE; BIOMECHANICAL PROPERTIES; TRABECULAR ARCHITECTURE; BONE MINERALIZATION; CANCELLOUS BONE; CORTICAL BONE; COMPACT-BONE; DENSITY; POROSITY;
D O I
10.1016/j.bone.2009.12.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The intra-specimen spatial variation in mineralization of bone tissue can be changed by drug treatments that alter bone remodeling. However, the contribution of such changes to the overall biomechanical effect of a treatment on bone strength is not known. To provide insight into this issue, we used a rat model to determine the effects of ovariectomy, parathyroid hormone, and raloxifene (vs. sham) on the contribution of spatial variations in mineralization to treatment-induced changes in vertebral stiffness. Mineral density was measured from 6-mu m voxel-sized quantitative micro-CT scans. Whole-vertebral and trabecular stiffness values were estimated using finite element analysis of these micro-CT scans, first including all intra-specimen variations in mineral density in the model and then excluding such variations by using a specimen-specific average density throughout each specimen. As expected, we found appreciable effects of treatment on overall bone stiffness, the effect being greater for the trabecular compartment (up to 52% reduction vs. sham, p<0.0001) than the whole vertebra (p = 0.055). Intra-specimen mean mineralization was not changed with treatment but the intra-specimen variation in mineralization was, although the effect was small (4%). Intra-specimen spatial variations in mineralization accounted for 10-12% and 5-6% of overall stiffness of the trabecular compartment and whole vertebral body, respectively. However, after accounting for all treatment effects on bone geometry and trabecular microstructure, any treatment effects due to changes in mineralization were negligible (<2%), although statistically detectable (p<0.02). We conclude that, despite a role in the general biomechanical behavior of bone, the spatial variations in tissue mineralization, as measured by quantitative micro-CT, did not appreciably contribute to ovariectomy-, PTH-, or raloxifene-induced changes in stiffness of the whole bone or the trabecular compartment in these rat vertebrae. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1162 / 1169
页数:8
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