TY - JOUR
T1 - Intracortical Bone Mechanics Are Related to Pore Morphology and Remodeling in Human Bone
AU - Bakalova, Lydia P.
AU - Andreasen, Christina M.
AU - Thomsen, Jesper Skovhus
AU - Brüel, Annemarie
AU - Hauge, Ellen Margrethe
AU - Kiil, Birgitte Jul
AU - Delaisse, Jean Marie
AU - Andersen, Thomas Levin
AU - Kersh, Mariana E.
N1 - We would like to thank Gete Ester Toft Eschen, from the Aarhus University Hospital, Denmark, for helping with obtaining the bone samples used in this research; and thanks to Jette Barlach, Kaja Laursen, and Birgit MacDonald, who assisted with the handling of the tissues. The μCT-scanner was donated by the VELUX Foundation. We also acknowledge the Velux Foundation (VELUX26922) for donation of the micro-CT scanner and funding support from the the Velux Foundation (VELUX34368), Danish Southern Region Research Grant (15/24851), Aase og Ejnar Danielses Foundation (10-001584), and the Burroughs Wellcomme Fund (1017487). Authors’ roles: The study was designed by MEK, TLA, and JST. The bone specimens were obtained by EMH and BJK. The analysis was conducted by LPB, CMA, and JST, who also take responsibility for the integrity of the data analysis. The data were analyzed by LPB, MEK, and TLA, and interpreted by all authors. The manuscript was drafted by MEK and TLA, and revised by all authors, who also approved the final version.
We would like to thank Gete Ester Toft Eschen, from the Aarhus University Hospital, Denmark, for helping with obtaining the bone samples used in this research; and thanks to Jette Barlach, Kaja Laursen, and Birgit MacDonald, who assisted with the handling of the tissues. The µCT-scanner was donated by the VELUX Foundation. We also acknowledge the Velux Foundation (VELUX26922) for donation of the micro-CT scanner and funding support from the the Velux Foundation (VELUX34368), Danish Southern Region Research Grant (15/24851), Aase og Ejnar Danielses Foundation (10-001584), and the Burroughs Wellcomme Fund (1017487).
PY - 2018/12
Y1 - 2018/12
N2 - During aging and in osteoporosis, cortical bone becomes more porous, making it more fragile and susceptible to fractures. The aim of this study was to investigate the intracortical compression- induced strain energy distribution, and determine whether intracortical pores associated with high strain energy density (SED) in the surrounding bone matrix have a different morphology and distribution, as well as different remodeling characteristics than matrix with normal SED. Fibular diaphyseal specimens from 20 patients undergoing a jaw reconstruction (age range 41 to 75 years; 14 men and 6 women) were studied. Bone specimens were µCT-scanned, plastic embedded, and sectioned for histology. Three-dimensional microfinite element models of each specimen were tested in compression, and the SED of the bone immediately surrounding the intracortical pores was calculated within a plane of interest corresponding to the histological sections. The SED of a pore, relative to the distribution of the SED of all pores in each specimen, was used to classify pores as either a high or normal SED pore. Pores with high SED were larger, less circular, and were located closer to the endosteal surface of the cortex than normal SED pores (p < 0.001). Histological analysis of the remodeling events generating the pores revealed that the high SED pores compared with normal SED pores had 13.3-fold higher odds of being an erosive (70%) or formative (7%) pore versus a quiescent pore (p < 0.001), 5.9-fold higher odds of resulting from remodeling upon existing pores (type 2 pore) versus remodeling generating new pores (type 1 pore) (p < 0.001), and 3.2-fold higher odds of being a coalescing type 2 pore versus a noncoalescing type 2 pore (p < 0.001). Overall, the study demonstrates a strong relationship between cortical bone mechanics and pore morphology, distribution, and remodeling characteristics in human fibular bone.
AB - During aging and in osteoporosis, cortical bone becomes more porous, making it more fragile and susceptible to fractures. The aim of this study was to investigate the intracortical compression- induced strain energy distribution, and determine whether intracortical pores associated with high strain energy density (SED) in the surrounding bone matrix have a different morphology and distribution, as well as different remodeling characteristics than matrix with normal SED. Fibular diaphyseal specimens from 20 patients undergoing a jaw reconstruction (age range 41 to 75 years; 14 men and 6 women) were studied. Bone specimens were µCT-scanned, plastic embedded, and sectioned for histology. Three-dimensional microfinite element models of each specimen were tested in compression, and the SED of the bone immediately surrounding the intracortical pores was calculated within a plane of interest corresponding to the histological sections. The SED of a pore, relative to the distribution of the SED of all pores in each specimen, was used to classify pores as either a high or normal SED pore. Pores with high SED were larger, less circular, and were located closer to the endosteal surface of the cortex than normal SED pores (p < 0.001). Histological analysis of the remodeling events generating the pores revealed that the high SED pores compared with normal SED pores had 13.3-fold higher odds of being an erosive (70%) or formative (7%) pore versus a quiescent pore (p < 0.001), 5.9-fold higher odds of resulting from remodeling upon existing pores (type 2 pore) versus remodeling generating new pores (type 1 pore) (p < 0.001), and 3.2-fold higher odds of being a coalescing type 2 pore versus a noncoalescing type 2 pore (p < 0.001). Overall, the study demonstrates a strong relationship between cortical bone mechanics and pore morphology, distribution, and remodeling characteristics in human fibular bone.
KW - CORTICAL BONE
KW - FINITE ELEMENT
KW - MICROSTRUCTURE
KW - POROSITY
KW - STRENGTH
UR - https://www.scopus.com/pages/publications/85052784834
UR - https://www.scopus.com/pages/publications/85052784834#tab=citedBy
U2 - 10.1002/jbmr.3561
DO - 10.1002/jbmr.3561
M3 - Article
C2 - 30048570
AN - SCOPUS:85052784834
SN - 0884-0431
VL - 33
SP - 2177
EP - 2185
JO - Journal of Bone and Mineral Research
JF - Journal of Bone and Mineral Research
IS - 12
ER -