s / Osteoarthritis and Cartilage 21 (2013) S63–S312 S75 active ADAMTS-4 where surface fibrillation and clustered chondrocytes were observed and lost when there was no proteoglycan observed. MMP-9 staining was strong throughout the OA sections when pronounced OA characteristics, such as fibrillation, erosion and hypertrophy, were present Conclusions: Better understanding on the dynamics of proteolytical activity profiles in OA cartilage may aid in improved insight to joint pathology. This should lead to enhanced targeting of novel intervention for OA. 123 THE RELATIONSHIP BETWEEN SYNOVIAL FLUID ARGS, CYTOKINES, MMPS & TIMPS FOLLOWING ACUTE ACL INJURY T.W. Tourville y, R.J. Johnson y, J.R. Slauterbeck y, S. Naud y, L.S. Lohmander z,x, A. Struglics z, B.D. Beynnon y. yUniv. of Vermont Coll. of Med., Burlington, VT, USA; z Lund Univ., Dept. of Orthopaedics, Clinical Sci. Lund, Lund, Sweden; xRes. Unit for Musculoskeletal Function and Physiotherapy, Inst. for Sports and Clinical Biomechanics, Univ. of Southern Denmark, Denmark, Sweden Purpose: Injury to the Anterior Cruciate Ligament (ACL) results in a high incidence of Post-Traumatic Osteoarthritis (PTOA). Limited information is available regarding the role of inflammatory mediators in PTOA, especially during the onset and earliest stages of the disease process. Recent investigations have provided evidence that a biochemical response occurs very soon after acute knee trauma, and aggrecan degradation (evidenced by elevated levels of synovial fluid (SF) aggrecanase generated N-terminal ARGS) is associated with inflammatory activity during the initial few weeks following acute ACL rupture. It is not known, however, if this process persists for a longer time interval following trauma; if ARGS concentrations are associated with additional cytokines not previously described; or how ARGS concentrations relate to levels of matrix metalloproteases (MMPs) or tissue inhibitors of metalloproteases (TIMPs) found in the synovial fluid following ACL disruption. Consequently, the purpose of this study was to evaluate relationships between SF ARGS levels and an array of cytokines, MMPs and TIMPs within the 6 months following acute ACL rupture. Methods: Synovial fluid samples from 67 ACL-injured patients (29 women) were used for analysis in this exploratory, cross sectional study. Entry criteria included: Age at the time of enrollment 1⁄4 1455yrs; BMI 1⁄4 18.5-30, Tegner score > 4; no relevant knee pathologies other than the index ACL injury; normal lower extremity alignment; and relatively minor articular cartilage and meniscal pathologies. All samples were obtained within 6 months of injury (18-155 days) via non-lavage arthrocentesis immediately prior to surgical ACL reconstruction. SF samples were analyzed for ARGS concentration via electrochemiluminescence immunoassay. Concentrations of 42 different cytokines were evaluated using commercially available Luminex-based multiplex analysis kits (42-Plex), as were 8 MMPs (panels 1 & 2), and 4 TIMPs (panel 1) (Millipore, Billerica, MA). Relationships between ARGS concentrations and individual analyte concentrations as well as MMP/TIMP ratios were evaluated statistically with partial Spearman Partial Correlation tests (rs), while adjusting for age, sex, and time since injury. This analysis technique was chosen because it is not strongly influenced by normality of data or “outliers.” Results: Statistically significant relationships were found between ARGS concentrations and FGF-2 (rs 1⁄4 -0.27, p 1⁄4 0.03) and TIMP-3 (rs 1⁄4 0.33, p 1⁄4 0.01). Although not statistically significant, FLT-3L, IP-10, and TIMP-1 had correlations greater than 0.20 (absolute values), trending toward significant correlations (Table 1). All other analytes tested received r-values less than 0.2 and were not significant.