Extended report
Comparative study of the synovial histology in rheumatoid
arthritis, spondyloarthropathy, and osteoarthritis: influence of
disease duration and activity
D Baetena, P Demetterb, C Cuvelierb, F Van den Boscha, E Kruithofa, N Van Dammea, G Verbruggena, H Mielantsa, E M Veysa, F De Keysera
a Department of
Rheumatology, University Hospital, University of Ghent, Belgium, b Department of Pathology,
University Hospital, University of Ghent, Belgium
Correspondence to: Dr D Baeten, Department of Rheumatology, 0K12IB, University Hospital Ghent, De Pintelaan 185, 9000 Ghent, Belgium dominique.baeten{at}rug.ac.be
Accepted for publication 1 May 2000
OBJECTIVES
To compare
the macroscopic and microscopic characteristics of synovial tissue in
rheumatoid arthritis (RA), spondyloarthropathy (SpA), and
osteoarthritis (OA) after exclusion of possible biases induced by
disease duration or activity, or both.
METHODS
Synovial
biopsy specimens were obtained by needle arthroscopy in patients with
early RA (n=16), late RA (n=14), early SpA (n=23), and OA (n=12).
Macroscopic and microscopic features were scored on a four point scale
and analysed as a function of disease duration (early versus late RA),
local and systemic disease activity, and diagnosis.
RESULTS
Except for the
maximal synovial lining thickness, no significant differences were seen
between early and late RA. For disease activity, synovial histology was
only weakly correlated with C reactive protein in RA, but seemed to be
strongly dependent on effusion of the biopsied joint in all disease
groups. After stratification for local disease activity, no disease
related differences were found in patients without joint effusion. In
contrast, important differences were found between patients with RA and
SpA with active joint effusion. Synovial vascularity was
macroscopically increased in SpA versus RA (p=0.017). A straight vessel
pattern was only seen in RA, while tortuous vessels were preferentially
seen in SpA. Vascularity was also microscopically increased in SpA
compared with RA (p=0.031), and correlated with the macroscopic
vascularity (rs=0.36, p=0.036).
CD3+ (p=0.008), CD4+ (p=0.008), and CD20+ (p=0.024) lymphocytes were
overrepresented in RA compared with SpA. The integrin expression in RA
was characterised by a decrease of
V
3 in the synovial lining
(p=0.006) and an increase of
V
5 in the sublining (p<0.001).
CONCLUSIONS
The immune
architecture of the synovial membrane is more dependent on local
disease activity than on disease duration. Synovium obtained from
clinically affected joints shows important histological differences
between RA and SpA.
© 2000 by Annals of the Rheumatic Diseases
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