Application of ultrasound transit time spectroscopy to human cancellous bone for derivation of bone volume fraction in-vitro

2015 ◽  
Vol 137 (4) ◽  
pp. 2285-2285 ◽  
Author(s):  
Christian M. Langton ◽  
Marie-Luise Wille
2020 ◽  
Vol 143 (2) ◽  
Author(s):  
Matthew B. L. Bennison ◽  
A. Keith Pilkey ◽  
W. Brent Lievers

Abstract Cancellous bone is an anisotropic structure with architectural and mechanical properties that vary due to both skeletal site and disease state. This anisotropy means that, in order to accurately and consistently measure the mechanical properties of cancellous bone, experiments should be performed along the primary mechanical axis (PMA), that is, the orientation in which the mechanical properties are at their maximum value. Unfortunately, some degree of misalignment will always be present, and the magnitude of the resulting error is expected to be architecture dependent. The goal of this work is to quantify the dependence of the misalignment error, expressed in terms of change in apparent elastic modulus (ΔE), on both the bone volume fraction (BV/TV) and the degree of anisotropy (DA). Finite element method (FEM) models of bovine cancellous bone from five different skeletal sites were created at 5 deg and 20 deg from the PMA determined for each region. An additional set of models was created using image dilation/erosion steps in order to control for BV/TV and better isolate the effect of DA. Misalignment error was found to increase with increasing DA and decreasing BV/TV. At 5 deg misaligned from the PMA, error is relatively low (<5%) in all cases but increases to 8–24% error at 20 deg. These results suggest that great care is needed to avoid introducing misalignment error into experimental studies, particularly when studying regions with high anisotropy and/or low bone volume fraction, such as vertebral or osteoporotic bone.


2005 ◽  
Vol 127 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Yener N. Yeni ◽  
Gregory T. Christopherson ◽  
X. Neil Dong ◽  
Do-Gyoon Kim ◽  
David P. Fyhrie

The level of structural detail that can be acquired and incorporated in a finite element (FE) analysis might greatly influence the results of microcomputed tomography (μCT)-based FE simulations, especially when relatively large bones, such as whole vertebrae, are of concern. We evaluated the effect of scanning and reconstruction voxel size on the μCT-based FE analyses of human cancellous tissue samples for fixed- and free-end boundary conditions using different combinations of scan/reconstruction voxel size. We found that the bone volume fraction (BV/TV) did not differ considerably between images scanned at 21 and 50 μm and reconstructed at 21, 50, or 110 μm (−0.5% to 7.8% change from the 21/21 μm case). For the images scanned and reconstructed at 110 μm, however, there was a large increase in BV/TV compared to the 21/21 μm case (58.7%). Fixed-end boundary conditions resulted in 1.8% [coefficient of variation (COV)] to 14.6% (E) difference from the free-end case. Dependence of model output parameters on scanning and reconstruction voxel size was similar between free- and fixed-end simulations. Up to 26%, 30%, 17.8%, and 32.3% difference in modulus (E), and average (VMExp), standard deviation (VMSD) and coefficient of variation (COV) of von Mises stresses, respectively, was observed between the 21/21 μm case and other scan/reconstruction combinations within the same (free or fixed) simulation group. Observed differences were largely attributable to scanning resolution, although reconstruction resolution also contributed significantly at the largest voxel sizes. All 21/21 μm results (taken as the gold standard) could be predicted from the 21/50 radj2=0.91-0.99;p<0.001, 21/110 radj2=0.58-0.99;p<0.02 and 50/50 results radj2=0.61-0.97;p<0.02. While BV/TV, VMSD, and VMExp/σz from the 21/21 could be predicted by those from the 50/110 radj2=0.63-0.93;p<0.02 and 110/110 radj2=0.41-0.77;p<0.05 simulations as well, prediction of E, VMExp, and COV became marginally significant 0.04<p<0.13 at 50/110 and nonsignificant at 110/110 0.21<p<0.70. In conclusion, calculation of cancellous bone modulus, mean trabecular stress, and other parameters are subject to large errors at 110/110 μm voxel size. However, enough microstructural details for studying bone volume fraction, trabecular shear stress scatter, and trabecular shear stress amplification VMExp/σz can be resolved using a 21/110 μm, 50/110 μm, and 110/110 μm voxels for both free- and fixed-end constraints.


2016 ◽  
Vol 13 (114) ◽  
pp. 20150991 ◽  
Author(s):  
Patrik Christen ◽  
Friederike A. Schulte ◽  
Alexander Zwahlen ◽  
Bert van Rietbergen ◽  
Stephanie Boutroy ◽  
...  

A bone loading estimation algorithm was previously developed that provides in vivo loading conditions required for in vivo bone remodelling simulations. The algorithm derives a bone's loading history from its microstructure as assessed by high-resolution (HR) computed tomography (CT). This reverse engineering approach showed accurate and realistic results based on micro-CT and HR-peripheral quantitative CT images. However, its voxel size dependency, reproducibility and sensitivity still need to be investigated, which is the purpose of this study. Voxel size dependency was tested on cadaveric distal radii with micro-CT images scanned at 25 µm and downscaled to 50, 61, 75, 82, 100, 125 and 150 µm. Reproducibility was calculated with repeated in vitro as well as in vivo HR-pQCT measurements at 82 µm. Sensitivity was defined using HR-pQCT images from women with fracture versus non-fracture, and low versus high bone volume fraction, expecting similar and different loading histories, respectively. Our results indicate that the algorithm is voxel size independent within an average (maximum) error of 8.2% (32.9%) at 61 µm, but that the dependency increases considerably at voxel sizes bigger than 82 µm. In vitro and in vivo reproducibility are up to 4.5% and 10.2%, respectively, which is comparable to other in vitro studies and slightly higher than in other in vivo studies. Subjects with different bone volume fraction were clearly distinguished but not subjects with and without fracture. This is in agreement with bone adapting to customary loading but not to fall loads. We conclude that the in vivo bone loading estimation algorithm provides reproducible, sensitive and fairly voxel size independent results at up to 82 µm, but that smaller voxel sizes would be advantageous.


1999 ◽  
Vol 32 (3) ◽  
pp. 323-326 ◽  
Author(s):  
Ming Ding ◽  
Anders Odgaard ◽  
Ivan Hvid

Author(s):  
Cesare Ciani ◽  
Paula A. Ramirez Marin ◽  
Stephen B. Doty ◽  
Susannah P. Fritton

Estrogen depletion has been shown to cause bone loss in the proximal metaphysis of the rat tibia [1,2]. A decrease in bone volume fraction is frequently reported, yet there is little analysis in the literature related to changes in microporosities during osteoporosis. Our recent work quantifying microporosity changes due to estrogen depletion has shown an increase in the lacunar-canalicular porosity surrounding osteocytes in the proximal metaphysis of the rat tibia [3].


2008 ◽  
Vol 83 (6) ◽  
pp. 368-379 ◽  
Author(s):  
Ara Nazarian ◽  
Dietrich von Stechow ◽  
David Zurakowski ◽  
Ralph Müller ◽  
Brian D. Snyder

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Jingyan Fu ◽  
Matthew Goldsmith ◽  
Sequoia D. Crooks ◽  
Sean F. Condon ◽  
Martin Morris ◽  
...  

AbstractAnimals in space exploration studies serve both as a model for human physiology and as a means to understand the physiological effects of microgravity. To quantify the microgravity-induced changes to bone health in animals, we systematically searched Medline, Embase, Web of Science, BIOSIS, and NASA Technical reports. We selected 40 papers focusing on the bone health of 95 rats, 61 mice, and 9 rhesus monkeys from 22 space missions. The percentage difference from ground control in rodents was –24.1% [Confidence interval: −43.4, −4.9] for trabecular bone volume fraction and –5.9% [−8.0, −3.8] for the cortical area. In primates, trabecular bone volume fraction was lower by –25.2% [−35.6, −14.7] in spaceflight animals compared to GC. Bone formation indices in rodent trabecular and cortical bone were significantly lower in microgravity. In contrast, osteoclast numbers were not affected in rats and were variably affected in mice. Thus, microgravity induces bone deficits in rodents and primates likely through the suppression of bone formation.


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