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Published on: June 12, 2020
Age-dependent fatigue behaviour of human cortical bone
1Department of Biomedical Engineering, Jonsson Engineering Center, Room 7046, Rensselaer Polytechnic Institute, 110 8th Street, Troy, NY, 12180, USA.
Aging human bone shows an exponential decrease in fatigue life, with older bone exhibiting distinct stiffness loss patterns compared to younger bone. This age-related bone fragility is linked to differences in microcrack formation and damage mechanisms.
Area of Science:
- Biomedical Engineering
- Orthopedics
- Gerontology
Background:
- Bone quality is crucial for skeletal integrity, but age-related changes in bone's fatigue behavior remain poorly understood.
- Skeletal fragility increases with age, necessitating research into the underlying mechanisms of bone quality degradation.
Purpose of the Study:
- To investigate the age-dependent fatigue behavior of human bone.
- To identify damage mechanisms contributing to age-related bone fragility.
- To analyze stiffness loss and local tissue properties during fatigue loading in aging bone.
Main Methods:
- Four-point bending fatigue tests were performed on aging human bone samples.
- Stiffness loss was analyzed alongside nanoindentation measurements of local tissue stiffness.
- Histological evaluation assessed tensile and compressive damage to identify failure mechanisms.
Main Results:
- Fatigue life demonstrated an exponential decrease with increasing age.
- Older bone exhibited distinct modulus degradation profiles compared to younger bone.
- Younger bone showed diffuse damage and tensile stiffness loss, while older bone displayed linear microcracks and compressive stiffness loss.
Conclusions:
- Age-related bone fragility is significantly influenced by the propensity of older bone to form linear microcracks over diffuse damage.
- Differences in damage mechanisms and stiffness loss between young and old bone contribute to age-related skeletal fragility.
- Understanding these age-dependent fatigue behaviors is critical for developing interventions against osteoporosis and fractures.
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