Accumulation of in-vivo fatigue microdamage and its relation to biomechanical properties in ageing human cortical bone

Authors
Citation
P. Zioupos, Accumulation of in-vivo fatigue microdamage and its relation to biomechanical properties in ageing human cortical bone, J MICROSC O, 201, 2001, pp. 270-278
Citations number
26
Categorie Soggetti
Multidisciplinary
Journal title
JOURNAL OF MICROSCOPY-OXFORD
ISSN journal
00222720 → ACNP
Volume
201
Year of publication
2001
Part
2
Pages
270 - 278
Database
ISI
SICI code
0022-2720(200102)201:<270:AOIFMA>2.0.ZU;2-I
Abstract
Bone matrix accumulates microdamage in the form of microcracks as a result of everyday cyclic loading activities. In two very recent studies, which us ed conventional histological stains and light microscopy techniques, the am ount of this in-vivo microdamage in the cortices of long bones has been sho wn to increase with age. These articles have suggested that in-vivo microcr acks may have an effect on the material properties of the tissue. However, a precise quantitative relationship between the number of microcracks and t he mechanical properties of these same bones has not been produced before, and in particular the way the microcracks may affect the stiffness, the str ength or possibly the toughness of the tissue. This article presents an exa mination of the in-vivo microdamage in human bones by the use of laser scan ning confocal microscopy, which offers better discrimination and allows exa mination of the cracks in-situ. Quantification of in-vivo fatigue microcrac ks was performed by counting the microcrack numerical density and surface d ensity in specimens for which we have previously derived a full set of mech anical properties as a function of age. It is shown that bone microdamage r elates more to the toughness (measured by three different measures) of agei ng bone tissue than to its stiffness and strength. The result allows us (i) to re-evaluate the fragility of ageing human bone and put more emphasis on its energy-related resistance to fracture than perhaps on its stiffness or strength and also (ii) to understand more fully the causal relationship an d interactions between microcracks and tissue toughness.