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Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis.

Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Research Abstract Details 

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  • Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Abstract Text:

    bridgette d furmanBridgette D Furman,jens strandJens Strand,w chad hembreeW Chad Hembree,benjamin d wardBenjamin D Ward,farshid guilakFarshid Guilak,steven a olsonSteven A Olson,

    Posttraumatic arthritis is one of the most frequent causes of disability following joint trauma. The objective of this study was to develop a model of a closed articular fracture in the mouse knee joint to quantify the temporal sequence of joint degeneration in a model of posttraumatic arthritis. Closed intraarticular fractures were created in the tibial plateau of adult mice (C57BL/6) using a computer-controlled materials testing system and a custom-built indenter tip. Tibial plateau fractures were classified and imaged over time using high-resolution digital radiography. Animals were sacrificed at 2, 4, 8, and 50 weeks following fracture, and the experimental and contralateral control limbs were harvested for histology and micro-computed tomography (microCT) analysis. By radiographic analysis, tibial plateau fractures closely resembled clinical fractures. More complex and comminuted fractures correlated to significantly higher fracture energies. Histologic analysis demonstrated progressive joint degeneration as measured by a modified Mankin scale, with fibrillation and loss of proteoglycan in the articular cartilage. Subchondral bone thickening was also observed in experimental joints. The induction of a closed intraarticular fracture of the mouse tibial plateau generated a reproducible and clinically relevant joint injury that progressed to osteoarthritis-like changes by histologic and microCT evaluations. The ability to induce joint degeneration without an osteotomy or open arthrotomy provides a valuable new model for studying the natural sequelae of posttraumatic arthritis. Notably, the use of a murine model will facilitate the use of genetically modified animals for the investigation of specific genes implicated in the pathology of posttraumatic arthritis.

    Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Publishing Authors By Initials

    bd furmanBD Furman,j strandJ Strand,wc hembreeWC Hembree,bd wardBD Ward,f guilakF Guilak,sa olsonSA Olson,

    For similar disorders of environmental origin: wounds and injuries: fractures, bone: tibial fractures research abstracts see: disorders of environmental origin: wounds and injuries: fractures, bone: tibial fractures research

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    Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of orthopaedic research : official publica

    VOLUME: 25

    Page Numbers: 578-92

    Journal Abbreviation:

    ISSN: 0736-0266

    DAY: 3

    MONTH: May

    YEAR: 2007

    Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8404726

    Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Keywords Mesh Terms:

    KEYWORDS: Tibial Fractures

    MESH TERMS: radiography

    Chemical & Substance for Abstract: Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis. Information

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    Grant and Affiliation Information for Joint degeneration following closed intraarticular fracture in the mouse knee: a model of posttraumatic arthritis.

    AFFILIATION: Division of Orthopaedic Surgery, Department of Surgery, Duke University Medical Center, Box 3389, Durham, North Carolina 27710, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAMS

    GRANT: AR50245

    ACRONYM: AR

    MEDLINETA: J Orthop Res

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