A study on the changes in the microstructure of trabecular bone and the biomechanical properties in patients with osteoporotic fractures and the correlation between them
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Updated: Nov 1, 2026

Trabecular Bone Microarchitecture Evaluation in an Osteoporosis Mouse Model
Published on: September 8, 2023
Hao Liu1,2, Xu Zhang1,2, Wenjie Xu1,2
1Department of Orthopedic, Yueyang Hospital Affiliated to Hunan Normal University, Yueyang, Hunan, China.
Objective:
To explore bone-quality characteristics in patients with osteoporotic femoral neck fractures by investigating trabecular-bone microstructural and biomechanical alterations of femoral-head specimens and their correlations.
Methods:
Femoral-head specimens from 20 patients with osteoporotic femoral neck fractures (experimental group: 69-90 years, 80.65 ± 8.85 years) and 13 patients with early-stage hip degenerative changes (control group: 49-83 years, 64.08 ± 6.93 years) were included. Noticeable baseline age imbalance existed between groups. All specimens underwent Micro-CT scanning. Cylindrical 8-mm-diameter trabecular-bone samples were harvested along principal compressive trabeculae. Compression, bending and torsion tests were conducted to acquire microstructural and biomechanical parameters.
Results:
Compared with controls, the experimental group exhibited significantly lower bone volume fraction (BV/TV), trabecular number (Tb.N), trabecular thickness (Tb.Th), alongside higher trabecular separation (Tb.Sp) and structural model index (SMI) (all P< 0.05). Biomechanical indicators including maximum compressive stress (MCL), maximum bending force (Fmax) and maximum torque (RST) were markedly reduced in the experimental group (P < 0.05). Trabecular microstructural indices were significantly correlated with biomechanical performance. Of note, baseline age imbalance and potential confounding from hip degenerative pathology should be considered when interpreting inter-group differences.
Conclusion:
This ex-vivo specimen-based study demonstrates severe trabecular deterioration and impaired biomechanical properties in osteoporotic-fracture specimens, with significant correlations between microstructural damage and reduced mechanical performance. These observations only reflect bone-quality features of isolated specimens; direct extrapolation to predict individual in-vivo fracture risk should be avoided.
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