Abnormal Microarchitecture and Reduced Stiffness at the Radius and Tibia in Postmenopausal Women With Fractures
Abnormal Microarchitecture and Reduced Stiffness at the Radius and Tibia in Postmenopausal Women With Fractures
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DOI:
10.1002/jbmr.152
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发表时间:
2010-12-01
影响因子:
6.2
通讯作者:
Shane, Elizabeth
中科院分区:
文献类型:
--
作者:
Stein, Emily M.;Liu, X. Sherry;Shane, Elizabeth
Measurement of areal bone mineral density (aBMD) by dual-energy x-ray absorptiometry (DXA) has been shown to predict fracture risk High-resolution peripheral quantitative computed tomography (HR-pQCT) yields additional information about volumetric BMD (vBMD), microarchitecture, and strength that may increase understanding of fracture susceptibility Women with (n=68) and without (n=101) a history of postmenopausal fragility fracture had aBMD measured by DXA and trabecular and cortical vBMD and trabecular microarchitecture of the radius and tibia measured by HR-pQCT Finite-element analysis (FEA) of HR-pQCT scans was performed to estimate bone stiffness DXA T-scores were similar in women with and without fracture at the spine, hip, and one-third radius but lower in patients with fracture at the ultradistal radius (p < 01) At the radius fracture, patients had lower total density, cortical thickness, trabecular density, number, thickness, higher trabecular separation and network heterogeneity (p < 0001 to 04) At the tibia, total, cortical, and trabecular density and cortical and trabecular thickness were lower in fracture patients (p < 0001 to 03) The differences between groups were greater at the radius than at the tibia for inner trabecular density, number, trabecular separation, and network heterogeneity (p < 01 to 05) Stiffness was reduced in fracture patients, more markedly at the radius (41% to 44%) than at the tibia (15% to 20%) Women with fractures had reduced vBMD, microarchitectural deterioration, and decreased strength These differences were more prominent at the radius than at the tibia HR-pQCT and FEA measurements of peripheral sites are associated with fracture prevalence and may increase understanding of the role of microarchitectural deterioration in fracture susceptibility (C) 2010 American Society for Bone and Mineral Research