4.6 Article

Cortical thinning and accumulation of large cortical pores in the tibia reflect local structural deterioration of the femoral neck

期刊

BONE
卷 137, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2020.115446

关键词

Cortical bone; Porosity; Bone strength; Finite element analysis; Hip fragility

资金

  1. Deutsche Forschungsgemeinschaft [DFG Ra1380/9-1, Gl 289/8-1]
  2. Agence Nationale de la Recherche [ANR-14-CE35-0030-01]
  3. Bundesministerium fur Bildung und Forschung (BMBF, musculoskeletal research network) within the subproject characterization of cortical and subchondral bone [01EC1408L]
  4. German Academic Exchange Service (DAAD) [91578351]
  5. Weijerhorst Foundation [WH2]
  6. Agence Nationale de la Recherche (ANR) [ANR-14-CE35-0030] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

Introduction: Cortical bone thinning and a rarefaction of the trabecular architecture represent possible causes of increased femoral neck (FN) fracture risk. Due to X-ray exposure limits, the bone microstructure is rarely measurable in the FN of subjects but can be assessed at the tibia. Here, we studied whether changes of the tibial cortical microstructure, which were previously reported to be associated with femur strength, are also associated with structural deteriorations of the femoral neck. Methods: The cortical and trabecular architectures in the FN of 19 humans were analyzed ex vivo on 3D microcomputed tomography images with 30.3 mu m voxel size. Cortical thickness (Ct.Th-tibia), porosity (Ct.Po-tibia) and pore size distribution in the tibiae of the same subjects were measured using scanning acoustic microscopy (12 mu m pixel size). Femur strength during sideways falls was simulated with homogenized voxel finite element models. Results: Femur strength was associated with the total (vBMD(tot); R-2 = 0.23, p < 0.01) and trabecular (vBMD(trab); R-2 = 0.26, p < 0.01) volumetric bone mineral density (vBMD), with the cortical thickness (Ct.Th-FN; R-2 = 0.29, p < 0.001) and with the trabecular bone volume fraction (Tb.BV/TVFN; R-2 = 0.34, p < 0.001), separation (Tb.Sp(FN); R-2 = 0.25, p < 0.01) and number (Tb.N-FN; R-2 = 0.32, p < 0.001) of the femoral neck. Moreover, smaller Ct.Th-tibia was associated with smaller CLThFN (R-2 = 0.31, p < 0.05), lower Tb.BV/TVFN (R-2 = 0.29, p < 0.05), higher Tb.Sp(FN) (R-2 = 0.33, p < 0.05) and lower Tb.N-FN (R-2 = 0.42, p < 0.01). A higher prevalence of pores with diameter > 100 mu m in tibial cortical bone (relCt.Po100 mu m-tibia) indicated higher Tb.Sp(FN) (R-2 = 0.36, p < 0.01) and lower Tb.N-FN (R-2 = 0.45, p < 0.01). Conclusion: Bone resorption and structural decline of the femoral neck may be identified in vivo by measuring cortical bone thickness and large pores in the tibia.

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