With the etiology of osteoporotic fractures as motivation, the goal of this
study was to characterize the mechanical behavior of human trabecular bone
after overloading. Specifically, we quantified the reductions in modulus a
nd strength and the development of residual deformations and determined the
dependence of these parameters on the applied strain and apparent density.
Forty cylindrical specimens of human L1 vertebral trabecular bone were des
tructively loaded in compression at 0.5% strain per second to strains of up
to 3.0% and then immediately unloaded to zero stress and reloaded. (An anc
illary experiment on more readily available bovine bone had been performed
previously to develop this testing protocol.) In general, the reloading str
ess-strain curve had a short initial nonlinear region with a tangent modulu
s similar to Young's modulus. This was followed by an approximately linear
region spanning to 0.7% strain, with a reduced residual modulus. The reload
ing curve always approached the extrapolated envelope of the original loadi
ng curve. Percent modulus reduction (between Young's and residual), a quant
itative measure of mechanical damage, ranged from 5.2 to 91.0% across the s
pecimens. It increased:with increasing plastic strain (r(2) = 0.97) but was
not related to modulus or apparent density. Percent strength reduction, in
the range of 3.6-63.8%, increased with increasing plastic strain (r(2) = 0
.61) and decreasing apparent density (r(2) = 0.23). The residual strains of
up to 1.05% depended strongly on applied strain (r(2) = 0.96). Statistical
comparisons with previous data for bovine tibial bone lend substantial gen
erality to these trends and provide an envelope of expected behavior for ot
her sites. In addition to providing a basis for biomechanical analysis of t
he effects of damage in trabecular bone at the organ level, these findings
support the concept that occasional overloads may increase the risk of frac
ture by substantially degrading the mechanical properties of the underlying
trabecular bone.