Elevated joint contact stress from residual articular incongruity following intra-articular fracture (IAF) is a critically important risk factor for post-traumatic OA (PTOA) that until recently could not be assessed, presenting a major obstacle to meaningful research aimed at improving treatment. The goals of the proposed research are to employ a clinically applicable measure of contact stress, obtained using computational discrete element analysis (DEA) methods, to diagnose patients at risk of PTOA following IAF and to develop and test methods of preventing elevated contact stress from joint incongruity. In retrospective studies of different lower extremity joints, DEA will be utilized to identify thresholds of joint contact stress above which PTOA is most highly likely (Specific Aim 1). To advance understanding of how elevated cumulative contact stress after IAF affects joint structure and biology to cause PTOA, prospective studies will be undertaken to correlate contact stress levels with morphologic articular surface changes detected on MRI, with alterations in serum and urine biomarkers, with radiographic changes, and with patient pain and function (Aim 2). The other two aims of this study will make important clinical steps to prevent elevated contact stress following IAF and thereby improve patient outcomes. New intra-operative techniques will be developed to assess the contact stress exposure associated with a given candidate IAF reduction during operations, to inform surgeons in their decision-making. These novel techniques will be based on deduced fragment poses from fluoroscopic images correlated with pre-operative CT models;contact stress estimates will be calculated with DEA. These techniques will be assessed on simulated fracture models and piloted in the operating room during IAF surgery and compared with conventional treatment (Aim 3). In a pilot clinical feasibility study, acute joint distraction using a ring fixator for severe tibial pilon fractures will be assessed using DEA, MRI and biomarkers to determine if temporarily sparing damaged articular surfaces from harmful joint contact stress after injury improves joint healing in such high energy IAFs (Aim 4).

Public Health Relevance

Completion of these studies has the potential to change how IAFs are assessed and treated. Developing diagnostic tools to measure deleterious elevated contact stress that can be used in populations of patients will lead to better clinical research and improved patient care. In addition to forming the basis for improved treatments of IAF, information gained from these studies will advance understanding of the role of cumulative contact stress in all forms of OA.

National Institute of Health (NIH)
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Specialized Center (P50)
Project #
Application #
Study Section
Special Emphasis Panel (ZAR1-KM)
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of Iowa
Iowa City
United States
Zip Code
Yu, Y; Zheng, H; Buckwalter, J A et al. (2014) Single cell sorting identifies progenitor cell population from full thickness bovine articular cartilage. Osteoarthritis Cartilage 22:1318-26
Jang, Kee W; Buckwalter, Joseph A; Martin, James A (2014) Inhibition of cell-matrix adhesions prevents cartilage chondrocyte death following impact injury. J Orthop Res 32:448-54
Wang, Xiayi; Ayati, Bruce P; Brouillete, Marc J et al. (2014) Modeling and simulation of the effects of cyclic loading on articular cartilage lesion formation. Int J Numer Method Biomed Eng 30:927-41
Jang, Kee W; Ding, Lei; Seol, Dongrim et al. (2014) Low-intensity pulsed ultrasound promotes chondrogenic progenitor cell migration via focal adhesion kinase pathway. Ultrasound Med Biol 40:1177-86
Ding, Lei; Guo, Danping; Homandberg, Gene A et al. (2014) A single blunt impact on cartilage promotes fibronectin fragmentation and upregulates cartilage degrading stromelysin-1/matrix metalloproteinase-3 in a bovine ex vivo model. J Orthop Res 32:811-8
Anderson, Donald D; Thomas, Thaddeus P; Campos Marin, Ana et al. (2014) Computational techniques for the assessment of fracture repair. Injury 45 Suppl 2:S23-31
Diestelmeier, B W; Rudert, M J; Tochigi, Y et al. (2014) An instrumented pendulum system for measuring energy absorption during fracture insult to large animal joints in vivo. J Biomech Eng 136:064502
Brouillette, M J; Ramakrishnan, P S; Wagner, V M et al. (2014) Strain-dependent oxidant release in articular cartilage originates from mitochondria. Biomech Model Mechanobiol 13:565-72
Zhou, Cheng; Zheng, Hongjun; Seol, Dongrim et al. (2014) Gene expression profiles reveal that chondrogenic progenitor cells and synovial cells are closely related. J Orthop Res 32:981-8
Westerlind, Brian; Karam, Matthew; Anderson, Donald et al. (2014) A surgical skills training curriculum for PGY-1 residents: AAOS exhibit selection. J Bone Joint Surg Am 96:e140

Showing the most recent 10 out of 50 publications