MAGNETIC-RESONANCE IMAGING-DETERMINED SYNOVIAL-MEMBRANE AND JOINT EFFUSION VOLUMES IN RHEUMATOID-ARTHRITIS AND OSTEOARTHRITIS - COMPARISON WITH THE MACROSCOPIC AND MICROSCOPIC APPEARANCE OF THE SYNOVIUM
M. Ostergaard et al., MAGNETIC-RESONANCE IMAGING-DETERMINED SYNOVIAL-MEMBRANE AND JOINT EFFUSION VOLUMES IN RHEUMATOID-ARTHRITIS AND OSTEOARTHRITIS - COMPARISON WITH THE MACROSCOPIC AND MICROSCOPIC APPEARANCE OF THE SYNOVIUM, Arthritis and rheumatism, 40(10), 1997, pp. 1856-1867
Objective. To evaluate the relationship between synovial membrane and
joint effusion volumes determined by magnetic resonance imaging (MRI)
and macroscopic and microscopic synovial pathologic findings in patien
ts with rheumatoid arthritis (RA) and osteoarthritis (OA). Methods. Sy
novial biopsies were performed, and macroscopic grades of synovitis as
signed, at preselected knee sites during arthroscopy or arthrotomy in
17 knees with RA and 25 with OA, Synovial inflammation and 9 separate
tissue characteristics were graded histologically. Synovial membrane a
nd joint effusion volumes were determined by preoperative MRI, enhance
d with intravenous gadopentetate dimeglumine. Results. MRI-determined
synovial membrane volumes were correlated with the overall histologic
assessment of synovial inflammation (Spearman's sigma = 0.55, P < 0.00
1), with fibrin deposition, with subsynovial mononuclear and polymorph
onuclear leukocyte infiltration (sigma = 0.51-0.59), and less signific
antly with macroscopic synovitis, vessel proliferation, and granulatio
n tissue formation (sigma = 0.40-0.42), No correlation with synovial l
ining multiplication, perivascular edema, villous formation, or fibros
is was found (sigma < 0.30). Conclusions. MRI-determined synovial volu
mes are correlated with synovial inflammatory activity, Synovial volum
es probably mainly reflect the mass of cell-infiltrated, vascularized
subsynovial tissue, but may also be influenced by the cumulative synov
ial proliferative activity, MRT-determined synovial membrane and effus
ion volumes may be sensitive makers and/or predictors of disease activ
ity and treatment outcome in RA.