Method: The Multicenter Osteoarthritis (MOST) Study is a longitudinal observational study of subjects with OA or at risk of developing OA. The MRI protocol included axial and sagittal proton-density weighted fat-suppressed fast spin echo and coronal STIR sequences. MRI was performed at a 1.0 T extremity system. MRIs were assessed semiquantitatively according to the WORMS scoring system. Only knees without radiographic OA and no baseline tibio-femoral cartilage damage were included. A synovitis-surrogate of signal changes in the infrapatellar and intercondylar areas of Hoffa’s fat pad, and effusion were both scored from 0-3. Presence of definite synovitis and effusion was defined as any grade ≥ 2. Knees with scores of either 0 or 1 were the reference. Logistic regression was used to estimate the risk of cartilage loss at follow-up. Cartilage loss was defined as an increase of at least 0.5 grade (subtle within-grade progression, that did not fulfill the criteria of a full-grade change) in any subregion. Adjustment was performed for possible confounders of future tibio-femoral cartilage damage, i.e. baseline effusion for synovitis model, synovitis for effusion model, patellofemoral cartilage damage, meniscus damage, meniscal extrusion, body mass index, age, gender, malalignment, bone marrow lesions.
Results: 514 knees were included (55.6% women, mean age 60.1 ± 7.2, mean BMI 29.1 ± 4.5). 43 (8.4%) knees showed synovitis, and 53 (10.3%) presented with joint effusion at baseline. 137 (26.7%) knees showed cartilage loss at follow-up. After adjustment, baseline synovitis was not associated with an increased risk of cartilage loss at follow-up (adjusted odds ratio 1.0 [95% confidence intervals 0.5-2.1, p=0.89]). Knees with baseline effusion had an increased risk for cartilage loss (adjusted odds ratio 2.7 [95% confidence intervals 1.4-5.1, p=0.002]).
Conclusion: Baseline synovitis does not predict cartilage loss, but joint effusion. However, contrast-enhanced MRI, which is able to directly depict the inflamed synovium, might yield different results. Baseline effusion as a reflection of synovial activation seems to play a role in predicting structural progression in early or pre-OA.
Disclosure: F. W. Roemer, Boston Imgaing Core Lab, LLC, 4 ; A. Guermazi, Synarc, Inc., 1, Boston Imaging Core Lab, LLC, 4, MerckSerono; Facet Solutions , 5, GE HealthCare, 2 ; D. T. Felson, None; J. Niu, None; M. C. Nevitt, None; M. D. Crema, Boston Imaging Core Lab, LLC, 4 ; J. A. Lynch, None; C. Lewis, None; J. Torner, None; Y. Zhang, None.
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