Femoral head osteonecrosis remains a major unsolved problem in orthopedic surgery of the hip. Because total hip replacement often proves unsatisfactory for patients with this disorder, means are needed to forestall necrotic femoral head collapse. Much could be learned from an animal model reliably mimicking the human disorder's natural history of structural collapse. Existing quadrupedal models fail to replicate this key aspect of the pathogenesis, presumably owing to unduly benign biomechanical demand. Cryogenically-induced osteonecrosis in the emu, a large and very active biped, shows great promise for overcoming this difficulty. The central goal of the proposed work is to bring this new emu model optimally into concordance with human disorder.
Aim 1 is to establish quantitative linkage between cryo-insult parameters and resulting distributions of osteocyte death. This will involve thermal finite element analysis of temperature fields produced by a specially developed cryo-insult probe, and prediction of corresponding patterns of osteocyte death. Validation will be provided by osteocyte death distributions resulting from corresponding insults delivered intraoperatively.
Aim 2 is to quantify the functional similarity of femoral head mechanical load transmission in emus versus humans. In vivo joint loading of the emu hip will be determined from force plate and optoelectronic recordings. Bench tests will be performed to measure hip joint contact stress distributions, and to map cancellous bone stiffness distributions. A whole-gait-cycle structural finite element model of the emu femoral head will be developed, for comparison with corresponding data for the human.
Aim 3 is to compare the pathogenesis of osteonecrosis in emus with that in a (non-collapsing) canine model. Parameters of interest include the speed and patterns of revascularization, cell types, histomorphometric alterations of the trabecular lattice, and mechanical compromise.
Aim 4 is to correlate the speed and severity of collapse in the emu osteonecrosis model with quantifiable structural compromise. This will again involve the structural finite element model, coupled with CT-based assessments of bony structural degradation. At the project's conclusion, we expect to have filled a longstanding need in the field of osteonecrosis research: an animal model suitable for systematic study of human-implementable interventions to forestall femoral head collapse.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR049919-03
Application #
6869624
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Program Officer
Panagis, James S
Project Start
2003-04-01
Project End
2007-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
3
Fiscal Year
2005
Total Cost
$416,357
Indirect Cost
Name
University of Iowa
Department
Orthopedics
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Goetz, Jessica E; Robinson, Duane A; Pedersen, Douglas R et al. (2011) Cryoinsult parameter effects on the histologically apparent volume of experimentally induced osteonecrotic lesions. J Orthop Res 29:931-7
Troy, Karen L; Brown, Thomas D; Conzemius, Michael G (2009) Contact stress distributions on the femoral head of the emu (Dromaius novaehollandiae). J Biomech 42:2495-500
Goetz, Jessica E; Pedersen, Douglas R; Robinson, Duane A et al. (2008) The apparent critical isotherm for cryoinsult-induced osteonecrotic lesions in emu femoral heads. J Biomech 41:2197-205
Goetz, Jessica E; Derrick, Timothy R; Pedersen, Douglas R et al. (2008) Hip joint contact force in the emu (Dromaius novaehollandiae) during normal level walking. J Biomech 41:770-8
Troy, Karen L; Lundberg, Hannah J; Conzemius, Michael G et al. (2007) Habitual hip joint activity level of the penned EMU (Dromaius novaehollandie). Iowa Orthop J 27:17-23
Evans, Richard B; Conzemius, Michael G; Robinson, Duane A et al. (2006) Single-case experimental designs in veterinary research. Am J Vet Res 67:189-95