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236  BIOMECHANICS OF THE HUMAN BODY

                         It should be noted that the in vitro mechanical test methods most often used to date on trabecular
                       bone are known to introduce substantial errors in the data as a result of the porous anisotropic
                       trabecular structure. Damage preferentially occurs at the ends of machined specimens when they are
                       compressed between loading platens due to disruption of the trabecular network at the specimen
                       boundaries. 114–116  In addition, friction at the platen-specimen interface creates a triaxial stress state
                       that may result in an overestimation of modulus. 114,115,117  If strains are computed from the relative
                       displacement of the platens, substantial systematic and random errors in modulus on the order of
                       20 ± 12 percent can occur. 118  Strength and failure strain data are also affected. 119,120  The trabecular
                       anisotropy indicates that experimental measurements of the orthotropic elastic constants should be
                       done in the principal material coordinate system. Since off-axis moduli are functions of multiple
                       material elastic constants, substantial errors can be introduced from misalignment 121  if not corrected
                       for. Much of the data in the literature have been obtained in various types of off-axis configurations,
                       since specimens are often machined along anatomic rather than material axes. The difficulty in inter-
                       preting these off-axis measurements is heightened when intersite and interstudy comparisons are
                       attempted. For all these reasons, and since the in vitro test boundary conditions rarely replicate those
                       in vivo, interpretation and application of available data must be done with care.
                         An important development for structural analysis of whole bones is the use of quantitative
                       computed tomography (QCT) to generate anatomically detailed models of whole bone 122–127  or
                       bone-implant 128,129  systems. At the basis of such technology is the ability to use QCT to noninva-
                       sively predict the apparent density and mechanical properties of trabecular bone. Some studies have
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                       reported excellent predictions (r ≥ 0.75) of modulus and strength from QCT density information for
                       various anatomic sites. 82,89,130,131  Since the mechanical properties depend on volume fraction and
                       architecture, it is important to use such relations only for the sites for which they were developed;
                       otherwise, substantial errors can occur. Also, since QCT data do not describe any anisotropic
                       properties of the bone, trabecular bone is usually assumed to be isotropic in whole-bone and bone-
                       implant analyses. Typically, in such structural analyses, cortical bone properties are not assigned
                       from QCT since it does not have the resolution to discern the subtle variations in porosity and
                       mineralization that cause variations in cortical properties. In these cases, analysts typically assign
                       average properties, sometimes transversely isotropic, to the cortical bone.



           9.6 MECHANICAL PROPERTIES OF TRABECULAR
           TISSUE MATERIAL

                       While most biomechanical applications at the organ level require knowledge of material properties
                       at the scales described earlier, there is also substantial interest in the material properties of trabecular
                       tissue because this information may provide additional insight into diseases such as osteoporosis
                       and drug treatments designed to counter such pathologies. Disease- or drug-related changes could
                       be  most obvious at the tissue rather than apparent or whole-bone level, yet only recently have
                       researchers begun to explore this hypothesis. This is so primarily because the irregular shape and
                       small size of individual trabecula present great difficulties in measuring the tissue material properties.
                         Most of the investigations of trabecular tissue properties have addressed elastic behavior. Some
                       of the earlier experimental studies concluded that the trabecular tissue has a modulus on the order of
                       1 to 10 GPa. 132–135  Later studies using combinations of computer modeling of the whole specimen
                       and experimental measures of the apparent modulus have resulted in a wide range of estimated val-
                       ues for the effective modulus of the tissue (Table 9.6) such that the issue became controversial.
                       However, studies using ultrasound have concluded that values for elastic modulus are about 20 per-
                       cent lower than for cortical tissue. 136,137 This has been supported by results from more recent nanoin-
                       dentation studies. 61,62,138  The combined computer-experiment studies that successfully eliminated
                       end artifacts in the experimental protocols also found modulus values more typical of cortical bone
                       than the much lower values from the earlier studies. 139  Thus an overall consensus is emerging that
                       the elastic modulus of trabecular tissue is similar to, and perhaps slightly lower than, that of cortical
                       bone. 140  Regarding failure behavior, it appears from the results of combined computational-experimental
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