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Scientific Articles   |    
Distribution and Progression of Chondrocyte Damage in a Whole-Organ Model of Human Ankle Intra-Articular Fracture
Yuki Tochigi, MD, PhD1; Joseph A. Buckwalter, MS, MD2; James A. Martin, PhD3; Stephen L. Hillis, PhD4; Peng Zhang, MD3; Tanawat Vaseenon, MD1; Abigail D. Lehman, BS3; Thomas D. Brown, PhD1
1 Department of Orthopaedics and Rehabilitation (Y.T., T.V., and T.D.B.) and Department of Biomedical Engineering (T.D.B.), The University of Iowa, 2181 Westlawn, Iowa City, IA 52242. E-mail address for Y. Tochigi: yuki-tochigi@uiowa.edu
2 Department of Orthopaedics and Rehabilitation, The University of Iowa, 200 Hawkins Drive, Iowa City, IA 52242
3 Department of Orthopaedics and Rehabilitation, The University of Iowa, 1182 ML, Iowa City, IA 52242
4 The Center for Research in the Implementation of Innovative Strategies in Practice (CRIISP), VA Iowa City Medical Center, 152 VA, Iowa City, IA 52242
View Disclosures and Other Information
Disclosure: In support of their research for or preparation of this work, one or more of the authors received, in any one year, outside funding or grants in excess of $10,000 from the University of Iowa Biological Science Funding Program, the Orthopaedic Trauma Association (a research grant), and the National Institutes of Health (Grant P50 AR055533). Neither they nor a member of their immediate families received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity.

Investigation performed at The University of Iowa, Iowa City, Iowa

Copyright © 2011 by The Journal of Bone and Joint Surgery, Inc.
J Bone Joint Surg Am, 2011 Mar 16;93(6):533-539. doi: 10.2106/JBJS.I.01777
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Abstract

Background: 

Despite the best current treatments, intra-articular fractures commonly cause posttraumatic osteoarthritis. In this disorder, death and dysfunction of chondrocytes associated with acute cartilage injury presumably plays an important role in triggering the pathomechanical cascade that eventually leads to whole-joint degeneration. Information regarding this cell-level cartilage injury, particularly at the whole-organ level in actual human joints, has been lacking. In this study, the distribution and progression of fracture-associated cell-level cartilage damage were assessed using a novel whole-organ model of human ankle intra-articular fracture.

Methods: 

Seven normal human ankles harvested immediately following amputation were subjected to a transarticular compressive impaction insult that mimicked an injury mechanism typical of tibial plafond fractures. For each ankle, site-specific, time-dependent changes in chondrocyte viability in the fractured tibial surface were studied by means of live-dead assay, using a confocal laser-scanning microscope. Fractional chondrocyte death was measured at several time points, in the superficial zone of the cartilage in "fracture-edge" regions within 1 mm of the fracture lines, as well as in "non-fracture" regions more than 3 mm centrally away from the fracture lines.

Results: 

All seven experimental fractures morphologically replicated tibial plafond fractures. Immediately post-fracture, superficial-zone chondrocyte death was significantly greater (p = 0.001) in fracture-edge regions (fractional cell death = 7.6%) than in non-fracture regions (1.6%). Progression of cell death over the next forty-eight hours was significantly faster in fracture-edge regions (p = 0.007), with the fractional cell death reaching 25.9%, which was again significantly higher (p < 0.001) than in non-fracture regions (8.6%).

Conclusions: 

Cell-level cartilage damage in human intra-articular fractures was characterized by acute chondrocyte death that predominated along fracture lines and that spontaneously progressed in the forty-eight hours following injury.

Clinical Relevance: 

Progressive chondrocyte damage along fracture lines appears to be a reasonable target of therapeutic treatment to preserve the whole-joint cartilage metabolism in intra-articular fractures, eventually to mitigate the risk of posttraumatic osteoarthritis.

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    Accreditation Statement
    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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