scholarly journals A murine skeletal adaptation that significantly increases cortical bone mechanical properties. Implications for human skeletal fragility.

1993 ◽  
Vol 92 (4) ◽  
pp. 1697-1705 ◽  
Author(s):  
J Bonadio ◽  
K J Jepsen ◽  
M K Mansoura ◽  
R Jaenisch ◽  
J L Kuhn ◽  
...  

2018 ◽  
Vol 67 (3) ◽  
pp. R2 ◽  
Author(s):  
Jun IWAMOTO ◽  
Azusa SEKI ◽  
Tsuyoshi TAKEDA ◽  
Yoshihiro SATO ◽  
Harumoto YAMADA ◽  
...  


PLoS ONE ◽  
2011 ◽  
Vol 6 (1) ◽  
pp. e16359 ◽  
Author(s):  
R. Adam Horch ◽  
Daniel F. Gochberg ◽  
Jeffry S. Nyman ◽  
Mark D. Does


Bone Reports ◽  
2019 ◽  
Vol 11 ◽  
pp. 100220 ◽  
Author(s):  
Saeed Jerban ◽  
Yajun Ma ◽  
Erik W. Dorthe ◽  
Lena Kakos ◽  
Nicole Le ◽  
...  


Endocrinology ◽  
1996 ◽  
Vol 137 (4) ◽  
pp. 1358-1364 ◽  
Author(s):  
J Aerssens ◽  
R van Audekercke ◽  
M Talalaj ◽  
P Geusens ◽  
E Bramm ◽  
...  




PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e99262 ◽  
Author(s):  
Christopher L. Newman ◽  
Sharon M. Moe ◽  
Neal X. Chen ◽  
Max A. Hammond ◽  
Joseph M. Wallace ◽  
...  




2016 ◽  
Vol 138 (4) ◽  
Author(s):  
Ruoxun Fan ◽  
He Gong ◽  
Rui Zhang ◽  
Jiazi Gao ◽  
Zhengbin Jia ◽  
...  

Bone mechanical properties vary with age; meanwhile, a close relationship exists among bone mechanical properties at different levels. Therefore, conducting multilevel analyses for bone structures with different ages are necessary to elucidate the effects of aging on bone mechanical properties at different levels. In this study, an approach that combined microfinite element (micro-FE) analysis and macrocompressive test was established to simulate the failure of male rat femoral cortical bone. Micro-FE analyses were primarily performed for rat cortical bones with different ages to simulate their failure processes under compressive load. Tissue-level failure strains in tension and compression of these cortical bones were then back-calculated by fitting the experimental stress–strain curves. Thus, tissue-level failure strains of rat femoral cortical bones with different ages were quantified. The tissue-level failure strain exhibited a biphasic behavior with age: in the period of skeletal maturity (1–7 months of age), the failure strain gradually increased; when the rat exceeded 7 months of age, the failure strain sharply decreased. In the period of skeletal maturity, both the macro- and tissue-levels mechanical properties showed a large promotion. In the period of skeletal aging (9–15 months of age), the tissue-level mechanical properties sharply deteriorated; however, the macromechanical properties only slightly deteriorated. The age-related changes in tissue-level failure strain were revealed through the analysis of male rat femoral cortical bones with different ages, which provided a theoretical basis to understand the relationship between rat cortical bone mechanical properties at macro- and tissue-levels and decrease of bone strength with age.



Author(s):  
Qingwen Ni ◽  
Anahi Tinajero ◽  
Daniel P. Nicolella

A NMR spin-spin (T2) relaxation technique has been described for determining the porosity, mobile and the bound water distribution in baboon cortical bone and correlate to their mechanical properties. The technique of low-field proton NMR involves spin-spin relaxation and free induction decay (FID) measurements, and the computational inversion methods for decay data analysis. The advantages of using NMR T2 relaxation techniques for bone water distribution are illustrated. The CPMG T2 relaxation data can be inverted to T2 relaxation distribution and this distribution then can be transformed to a pore size distribution with the longer relaxation times corresponding to larger pores. The FID T2 relaxation data can be inverted to T2 relaxation distribution and this distribution then can be transformed to bound and mobile water distribution with the longest relaxation time corresponding to mobile water and the middle relaxation time corresponding to bound water. The technique is applied to quantify apparent changes in porosity, bound and mobile water in cortical bone. Overall bone porosity is determined using the calibrated NMR fluid volume from the proton relaxation data divided by overall bone volume. The NMR porosity, bound and mobile water components are determined from cortical bone specimens obtained from baboon donors of different ages, and the results are correlated to bone mechanical properties.



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