F. Buttgereit et al., VALUE OF ANTICARDIOLIPIN ANTIBODIES FOR MONITORING DISEASE-ACTIVITY IN SYSTEMIC LUPUS-ERYTHEMATOSUS AND OTHER RHEUMATIC DISEASES, Clinical rheumatology, 16(6), 1997, pp. 562-569
The prevalence of anticardiolipin antibodies in active systemic lupus
erythematosus (SLE) was compared with that in inactive SLE and other r
heumatic and non-rheumatic diseases to determine the value of these au
toantibodies in monitoring rheumatic diseases, Pairs of IgG-and IgM-aC
L were measured by ELISA in 173 consecutive hospitalised patients, inc
luding 141 with rheumatic diseases (18 active SLE, 21 inactive SLE, 19
rheumatoid arthritis, 13 reactive arthritis, 7 other spondyloarthropa
thies, 16 vasculitis, 47 other autoimmune diseases) and 32 non-rheumat
ic controls. A further 101 aCL pairs were determined during follow-up
in 19 patients with SLE. Serum concentrations were analysed with respe
ct to SLE activity and compared between the different patient groups,
IgG-and IgM-aCL levels in excess of 10 GPL and 9 MPL respectively were
considered positive, 30.6% of all patients (53/173) were found to be
positive for IgG-aCL, as against only 9.8% (17/173) for IgM-aCL. IgG-a
CL serum levels in active SLE differed significantly from all other gr
oups, including inactive SLE (all p < 0.005). Median IgM-aCL levels we
re below the cut off point in all groups, although measurable values w
ere obtained almost exclusively in active SLE and Ri, In this study Ig
M-aCL measurement was of less value in monitoring rheumatic diseases,
IgG-aCL positivity in SLE was associated with a significantly higher o
dds ratio (OR) for active disease (OR 16.0, 95% confidence interval: 2
.8-90.0). The results show that disease activity in SLE was accompanie
d by significantly increased IgG-aCL, whereas no elevation was found i
n other diseases. This parameter may therefore be useful in monitoring
SLE activity.