Age, gender, and bone lamellae elastic moduli

• Published in: Journal of orthopaedic research Vol. 18; no. 3; pp. 432 - 437
• Main Authors: Hoffler, C. E., Moore, K. E., Kozloff, K., Zysset, P. K., Goldstein, S. A.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.05.2000; Blackwell Publishing Ltd
• Subjects: Adult; Age Factors; Aged; Aged, 80 and over; Biomechanical Phenomena; Bone and Bones - physiology; Cells; Crystal microstructure; Diseases; Elastic moduli; Elasticity; Fatigue of materials; Female; Fracture toughness; Hardness; Humans; Male; Metabolism; Middle Aged; Sex Factors; Space life sciences; Tissue
• ISSN: 0736-0266; 1554-527X
• DOI: 10.1002/jor.1100180315

To enhance preventative and therapeutic strategies for metabolic bone diseases and bone fragility disorders, we began to explore the physical properties of bone tissue at the cellular level. Proximal femurs were harvested from 27 cadavera (16 male and 11 female) for in vitro measurement of the mechanical properties. We measured the variations in lamellar‐level elastic modulus and hardness in human bone as a function of age and gender to identify microstructural properties responsible for age and gender‐related reductions in the mechanical integrity. The lateral femoral necks were examined, and age, gender, height, body mass, and body mass index were not found to correlate with lamellar‐level elastic modulus or hardness. This result was consistent for osteonal, interstitial, and trabecular tissue. These data suggest that increased bone mass maintenance, known to occur in heavier individuals, is not accompanied by increases in the lamellar‐level elastic modulus or hardness. The independence of elastic modulus and hardness from age and gender suggests that age and gender‐related decreases in mechanical integrity do not involve alterations in elastic modulus or hard ness of the extracellular matrix. Lamellar‐level ultimate, fatigue, and fracture toughness properties should also be investigated. Other factors, such as tissue mass and organization, may also contribute to age and gender‐related decreases in the mechanical integrity.