Rheumatology Advance Access originally published online on May 2, 2006
Rheumatology 2006 45(12):1542-1548; doi:10.1093/rheumatology/kel137
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Bone oedema predicts erosive progression on wrist MRI in early RAa 2-yr observational MRI and NC scintigraphy study
Oulu University Hospital, Oulu, Finland and 1Rheumatism Foundation Hospital, Heinola, Finland.
Correspondence to: Kari Palosaari, MD, Department of Diagnostic Radiology, Oulu University Hospital, Kajaanintie 50, FIN-90029, BOX 50, Oulu, Finland. E-mail: kari.palosaari{at}oulu.fi
Objectives. To investigate if disease assessment by contrast-enhanced dynamic and static magnetic resonance imaging (MRI) and quantitative nanocolloid (NC) scintigraphy gives useful additional information in early rheumatoid arthritis (RA).
Methods. Twenty-seven patients with early RA (disease duration
12 months) were followed up for 1 yr and 24 of them for 2 yrs with contrast-enhanced MRI and NC scintigraphy of the wrist joint. Synovial inflammation was assessed by measuring time-dependent enhancement rates (E-rate) from dynamic MRI scans and technetium99m-labelled nanocolloid (99mTc-NC) uptake from scintigraphy scans. Synovial membrane hypertrophy, bone oedema and erosions were semiquantitatively scored according to the Outcome Measures in Rheumatology Clinical Trials RA-MRI scoring system from static MR images. Response to the treatment was evaluated based on whether or not
50% improvement was achieved in the tender and swollen joint scores and the Health Assessment Questionnaire score, with normal C-reactive protein (CRP) or erythrocyte sedimentation rate (ESR) levels. Progression of the erosion score on wrist MRI was evaluated as the outcome.
Results. The baseline MRI bone oedema score (
= 0.67), MRI synovitis score (
= 0.57), ESR (
= 0.56), CRP (
= 0.48), E-rate (
= 0.47) and 99mTc-NC uptake (
= 0.45) were related with the change in the MRI erosion score from baseline to 2 yrs (
= Spearman's correlation). In the multivariate logistic regression model, the bone marrow oedema score was the only baseline variable that predicted erosive progression at 2 yrs follow-up (OR 4.2, 95% CI 1.313.8). The median (interquartile range) change in the erosion score from baseline to 2 yrs was 0 (0, 0) and 4 (2, 5) in the patients with (n= 9) and without (n= 15) a persistent clinical response over the 2 yrs, respectively (P= 0.001). The non-responders who presented with erosive progression from 1 yr to 2 yrs had higher MRI synovitis scores, bone oedema scores, E-rate and 99mTc-NC uptake at 1-yr follow-up than the non-responders without progressive bone damage.
Conclusion. The degree of local synovial inflammation at baseline, evaluated by dynamic and static MRI and quantitative NC scintigraphy, is closely related to the progression of wrist joint erosions during the first 2 yrs of the disease. Furthermore, at follow-up, if no persistent clinical response is achieved, these imaging methods may help to predict future erosiveness and help in clinical therapeutic decision making.
KEY WORDS: MRI, NC scintigraphy, Rheumatoid arthritis, Follow-up
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