TY - JOUR
T1 - BMD-based assessment of local porosity in human femoral cortical bone
AU - Iori, Gianluca
AU - Heyer, Frans
AU - Kilappa, Vantte
AU - Wyers, Caroline
AU - Varga, Peter
AU - Schneider, Johannes
AU - Gräsel, Melanie
AU - Wendlandt, Robert
AU - Barkmann, Reinhard
AU - van den Bergh, J. P.
AU - Raum, Kay
N1 - Funding Information:
This work was supported by the Deutsche Forschungsgemeinschaft (DFG Ra1380/9-1 ), by the Bundesministerium für Bildung und Forschung (BMBF, musculoskeletal research network 01EC1408L , subproject “characterization of cortical and subchondral bone”), by the German Academic Exchange Service (DAAD, grant no. 91578351 ), and by the Weijerhors Foundation (grant no. WH2 ). We acknowledge Mario Thiele for the data archiving, Dr. Daniel Rohrbach for the scripts for BMD histogram analysis and Dr. Ahmed BenSaïda for the Matlab implementation of the Shapiro-Wilk test.
Publisher Copyright:
© 2018 Elsevier Inc.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/9
Y1 - 2018/9
N2 - Cortical pores are determinants of the elastic properties and of the ultimate strength of bone tissue. An increase of the overall cortical porosity (Ct.Po) as well as the local coalescence of large pores cause an impairment of the mechanical competence of bone. Therefore, Ct.Po represents a relevant target for identifying patients with high fracture risk. However, given their small size, the in vivo imaging of cortical pores remains challenging. The advent of modern high-resolution peripheral quantitative computed tomography (HR-pQCT) triggered new methods for the clinical assessment of Ct.Po at the peripheral skeleton, either by pore segmentation or by exploiting local bone mineral density (BMD). In this work, we compared BMD-based Ct.Po estimates with high-resolution reference values measured by scanning acoustic microscopy. A calibration rule to estimate local Ct.Po from BMD as assessed by HR-pQCT was derived experimentally. Within areas of interest smaller than 0.5 mm 2 , our model was able to estimate the local Ct.Po with an error of 3.4%. The incorporation of the BMD inhomogeneity and of one parameter from the BMD distribution of the entire scan volume led to a relative reduction of the estimate error of 30%, if compared to an estimate based on the average BMD. When applied to the assessment of Ct.Po within entire cortical bone cross-sections, the proposed BMD-based method had better accuracy than measurements performed with a conventional threshold-based approach.
AB - Cortical pores are determinants of the elastic properties and of the ultimate strength of bone tissue. An increase of the overall cortical porosity (Ct.Po) as well as the local coalescence of large pores cause an impairment of the mechanical competence of bone. Therefore, Ct.Po represents a relevant target for identifying patients with high fracture risk. However, given their small size, the in vivo imaging of cortical pores remains challenging. The advent of modern high-resolution peripheral quantitative computed tomography (HR-pQCT) triggered new methods for the clinical assessment of Ct.Po at the peripheral skeleton, either by pore segmentation or by exploiting local bone mineral density (BMD). In this work, we compared BMD-based Ct.Po estimates with high-resolution reference values measured by scanning acoustic microscopy. A calibration rule to estimate local Ct.Po from BMD as assessed by HR-pQCT was derived experimentally. Within areas of interest smaller than 0.5 mm 2 , our model was able to estimate the local Ct.Po with an error of 3.4%. The incorporation of the BMD inhomogeneity and of one parameter from the BMD distribution of the entire scan volume led to a relative reduction of the estimate error of 30%, if compared to an estimate based on the average BMD. When applied to the assessment of Ct.Po within entire cortical bone cross-sections, the proposed BMD-based method had better accuracy than measurements performed with a conventional threshold-based approach.
UR - http://www.scopus.com/inward/record.url?scp=85048250221&partnerID=8YFLogxK
U2 - 10.1016/j.bone.2018.05.028
DO - 10.1016/j.bone.2018.05.028
M3 - Journal articles
C2 - 29860154
AN - SCOPUS:85048250221
SN - 8756-3282
VL - 114
SP - 50
EP - 61
JO - Bone
JF - Bone
ER -