This is a basic scientific investigation of the patho-mechanistic etiology of post-traumatic osteoarthritis (PTOA) with particular emphasis on the role of acute mechanical damage. The long-term objectives of the study are to: 1)determine how acute mechanical damage is linked to PTOA;2) determine how acute mechanical damage affects the tolerance of articular cartilage to injury-associated changes in the long-term loading environment within a joint;and 3) investigate novel therapeutic options specifically designed to treat tissue-level and cellular-level damage associated with acutely impacted cartilage. A series of in vitro investigations will study the relative contribution of both acute damage and chronic loading abnormalities to cartilage degeneration. Potential adverse synergisitic interaction between these injury-associated residuals will also be investigated. Another in vitro study will investigate the role of matrix damage in the the cascade of injury propagation into surrounding uninjured cartilage. Finally, an established in vivo model will be used to investigate the patho-mechanistic link between acute mechanical damage, chronic abnormal loading, and the progression of PTOA, accounting for whole-joint effects that cannot be tested in parametric in vitro studies. The second part of the study will investigate therapeutic options that mechanically stabilize matrix damage and deliver targeted Pharmaceuticals into acutely damaged areas that foster chondrocytic anabolic metabolism and prevent chondrocyte apoptosis. These therapies will be studied in vitro, in a parametric study design that investigates treatment effectiveness with respect to impact energy and timing of treatment. To determine whole-joint effects, an in vivo porcine model of impact injury will be employed to study the same treatments. Post-traumatic osteoarthritis is a major cause of pain and dysfunction in a relatively young patient population. Therefore, it is also a major source of medical expenditure. Understanding the basic mechanisms that cause PTOA will facilitate development of more effective treatments. This study not only will further understanding the etiology of this devastating disease, it will provide new knowledge in a different treatment approach, focused on treating the acute mechanical damage. This study will investigate why injured joints develop arthritis. Furthermore, this study will investigate new treatment options that could potentially reduce or prevent arthritis in an injured joint.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Specialized Center (P50)
Project #
5P50AR055533-03
Application #
7920167
Study Section
Special Emphasis Panel (ZAR1)
Project Start
2009-09-01
Project End
2012-08-31
Budget Start
2009-09-01
Budget End
2010-08-31
Support Year
3
Fiscal Year
2009
Total Cost
$224,654
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Seol, Dongrim; Tochigi, Yuki; Bogner, Ashley M et al. (2018) Effects of knockout of the receptor for advanced glycation end-products on bone mineral density and synovitis in mice with intra-articular fractures. J Orthop Res 36:2439-2449
Thomas-Aitken, Holly D; Willey, Michael C; Goetz, Jessica E (2018) Joint contact stresses calculated for acetabular dysplasia patients using discrete element analysis are significantly influenced by the applied gait pattern. J Biomech 79:45-53
Coleman, Mitchell C; Goetz, Jessica E; Brouillette, Marc J et al. (2018) Targeting mitochondrial responses to intra-articular fracture to prevent posttraumatic osteoarthritis. Sci Transl Med 10:
Townsend, Kevin C; Thomas-Aitken, Holly D; Rudert, M James et al. (2018) Discrete element analysis is a valid method for computing joint contact stress in the hip before and after acetabular fracture. J Biomech 67:9-17
Ding, Lei; Buckwalter, Joseph A; Martin, James A (2017) DAMPs Synergize with Cytokines or Fibronectin Fragment on Inducing Chondrolysis but Lose Effect When Acting Alone. Mediators Inflamm 2017:2642549
Segal, Neil A; Frick, Eric; Duryea, Jeffrey et al. (2017) Comparison of tibiofemoral joint space width measurements from standing CT and fixed flexion radiography. J Orthop Res 35:1388-1395
Segal, Neil A; Bergin, John; Kern, Andrew et al. (2017) Test-retest reliability of tibiofemoral joint space width measurements made using a low-dose standing CT scanner. Skeletal Radiol 46:217-222
Dibbern, Kevin; Kempton, Laurence B; Higgins, Thomas F et al. (2017) Fractures of the tibial plateau involve similar energies as the tibial pilon but greater articular surface involvement. J Orthop Res 35:618-624
Kapitanov, Georgi I; Ayati, Bruce P; Martin, James A (2017) Modeling the effect of blunt impact on mitochondrial function in cartilage: implications for development of osteoarthritis. PeerJ 5:e3468
Martin, James A; Anderson, Donald D; Goetz, Jessica E et al. (2017) Complementary models reveal cellular responses to contact stresses that contribute to post-traumatic osteoarthritis. J Orthop Res 35:515-523

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