Increased Collagen Mineralization Affects the Yield Stress But Not the Yield Strain in Cortical Bone of Rats: Implications for Age-Related Tissue Embrittlement

Author(s):  
Ozan Akkus ◽  
Fran Adar ◽  
Mitchell B. Schaffler

It has been well documented that the fracture susceptibility of cortical bone increases significantly with age [1]. Although the age-related decline in the fracture resistance of the cortical bone is attributed to reduced bone quantity; a substantial overlap in the bone mass of normal subjects and those sustaining fractures suggests that bone mass alone does not identify the fracture risk on an individual basis [2]. Therefore, the conceptual framework should be improved to include bone quality measures in addition to bone quantity to refine fracture risk assessment. In this study, Raman microspectroscopy was used to assess two key variables of bone tissue quality in aging rat cortical bone: the relative amount of mineral with respect to the amount of collagen (i.e. collagen mineralization) and the mineral crystallinity (i.e. size and stoichiometric perfection of mineral crystals). In this regard the first aim of this study was to investigate age-related changes in the extent of mineralization of collagen fibers and to test its relationship to elastic deformability of cortical bone tissue. The second aim of the study was to investigate age-related changes in the mineral crystallinity and to test its relationship to elastic deformability of cortical bone tissue. The first hypothesis of this study is that both collagen mineralization and mineral crystallinity will increase with age. The second hypothesis of this study was that age-related changes in compositional properties will compromise the elastic deformation capacity of cortical bone tissue.

2000 ◽  
Vol 5 (1) ◽  
pp. 4-9 ◽  
Author(s):  
Jun Iwamoto ◽  
Tsuyoshi Takeda ◽  
Shoichi Ichimura ◽  
Yasunori Tsukimura ◽  
Yoshiaki Toyama

Bone ◽  
1999 ◽  
Vol 24 (4) ◽  
pp. 387-393 ◽  
Author(s):  
T Seck ◽  
A Bretz ◽  
R Krempien ◽  
B Krempien ◽  
R Ziegler ◽  
...  

Author(s):  
Maki Yokomoto-Umakoshi ◽  
Hironobu Umakoshi ◽  
Norifusa Iwahashi ◽  
Yayoi Matsuda ◽  
Hiroki Kaneko ◽  
...  

Abstract Purpose Dehydroepiandrosterone sulfate (DHEAS) from the adrenal cortex substantially decreases with age, which may accelerate osteoporosis. However, the association of DHEAS with bone mineral density (BMD) and fracture is inconclusive. We conducted a Mendelian randomization (MR) analysis to investigate the role of DHEAS in age-related changes in BMD and fracture risk. Methods Single nucleotide polymorphisms (SNPs) associated with serum DHEAS concentrations were used as instrumental variables (4 SNPs for main analysis; 4 SNPs for men and 5 SNPs for women in sex-related analysis). Summary statistics were obtained from relevant genome-wide association studies. Results A log-transformed unit (μmol/L) increase in serum DHEAS concentrations was associated with SD increase in estimated BMD at the heel (estimate, 0.120; 95% confidence interval [CI], 0.081–0.158; P = 9 × 10 -10), and decreased fracture (odds ratio [OR], 0.989; 95%CI, 0.981–0.996; P = 0.005), consistent with dual-energy X-ray absorptiometry-derived BMD at the femoral neck and lumbar spine. Their associations remained even after adjusting for height, body mass index, testosterone, estradiol, sex hormone-binding globulin, and IGF-1. The association of DHEAS with fracture remained after adjusting for falls, grip strength, and physical activity but was attenuated after adjusting for BMD. The MR-Baysian model averaging analysis showed BMD was the top mediating factor for association of DHEAS with fracture. The association between DHEAS and BMD was observed in men but not in women. Conclusion DHEAS was associated with increased BMD and decreased fracture. DHEAS may play a protective role in decreasing fracture risk, mainly by increasing bone mass.


Bone ◽  
2009 ◽  
Vol 44 ◽  
pp. S22
Author(s):  
K.K. Nishiyama ◽  
H.M. Macdonald ◽  
H.R. Buie ◽  
D.A. Hanley ◽  
S.K. Boyd

Author(s):  
Yener N. Yeni ◽  
Roger R. Zauel

Cortical bone tissue quality is imperative in maintaining the mechanical competence of whole bones, particularly at sites of overuse and age-related fragility fractures where a considerable cortical bone component is present. (Note that cortical bone tissue is more than 80% of the bone in the body [1].)


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