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Osteoporosis is often described as a dynamic imbalance in the activity of
osteoblasts, bone forming cells, and osteoclasts, cells that dissolve bone
tissue. This imbalance creates regions of low bone mass with an architecture
that is poorly suited to its mechanical function and leads to a dramatically
increased fracture risk. The development of effective therapies requires an
understanding of local effects including cellular-level phenomena and the
effects of mechanical loading and damage as well as system effects such as
parathyroid hormone and estrogen levels in the bloodstream. Perhaps even more
importantly, these processes occur over many different time scales and the
full effects of osteoporosis may not become apparent for decades.
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The goal of
this development project is to more fully understand how the cellular
processes of bone deposition and bone resorption lead to tissue-level and
organ-level bone structure. Towards this end computational models that
incorporate hierarchical length and time scales must be developed, calibrated
with existing experimental and in vivo results, and then tested to see if they
can predict clinical outcomes. This project will thus directly link the
mechanical behavior of bone generation at the cellular and macroscale levels
to molecular (hormonal) stimuli. For this project, Professor Nauman (an
experienced cell/tissue biomedical engineer) will collaborate with Professor
Hart, an expert in the use of the finite-element method for computing bone
remodeling processes.
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