TY - JOUR
T1 - Antibodies to β2-glycoprotein I and clinical manifestations in patients with systemic lupus erythematosus
AU - Tsutsumi, Akito
AU - Matsuura, Eiji
AU - Ichikawa, Kenji
AU - Fujisaku, Atsushi
AU - Mukai, Masaya
AU - Kobayashi, Seiichi
AU - Koike, Takao
PY - 1996/9
Y1 - 1996/9
N2 - Objective. To investigate whether anticardiolipin antibodies (aCL) in patients with systemic lupus erythematosus (SLE) bind to β2-glycoprotein I (β2GPI), and to search for a relationship between the presence of IgG and/or IgM anti-β2GPI antibody and clinical manifestations in SLE patients. Methods. IgG and IgM anti-β2GPI in 308 Japanese SLE patients were measured using phospholipid-independent enzyme immunoassays. Relationships to clinical histories and to various laboratory data were examined. Results. The values of anti-β2GPI and aCL, as measured by conventional enzyme immunoassay, showed a strong correlation, but the anti-β2GPI assay was more useful in distinguishing β2GPI-dependent aCL from β2GPI-independent aCL. The presence of IgG anti-β2GPI was associated with an increased frequency of a history of thrombosis. Comparisons of various laboratory data suggested that the titer of anti-β2GPI may fluctuate with disease activity. Conclusion. The results suggest that pathogenic aCL is directed against structurally altered β2GPI and that enzyme immunoassay for anti-β2GPI may prove useful in evaluating the risk of thrombosis and monitoring the clinical course in patients with SLE.
AB - Objective. To investigate whether anticardiolipin antibodies (aCL) in patients with systemic lupus erythematosus (SLE) bind to β2-glycoprotein I (β2GPI), and to search for a relationship between the presence of IgG and/or IgM anti-β2GPI antibody and clinical manifestations in SLE patients. Methods. IgG and IgM anti-β2GPI in 308 Japanese SLE patients were measured using phospholipid-independent enzyme immunoassays. Relationships to clinical histories and to various laboratory data were examined. Results. The values of anti-β2GPI and aCL, as measured by conventional enzyme immunoassay, showed a strong correlation, but the anti-β2GPI assay was more useful in distinguishing β2GPI-dependent aCL from β2GPI-independent aCL. The presence of IgG anti-β2GPI was associated with an increased frequency of a history of thrombosis. Comparisons of various laboratory data suggested that the titer of anti-β2GPI may fluctuate with disease activity. Conclusion. The results suggest that pathogenic aCL is directed against structurally altered β2GPI and that enzyme immunoassay for anti-β2GPI may prove useful in evaluating the risk of thrombosis and monitoring the clinical course in patients with SLE.
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U2 - 10.1002/art.1780390905
DO - 10.1002/art.1780390905
M3 - Article
C2 - 8814057
AN - SCOPUS:0029790008
SN - 2326-5191
VL - 39
SP - 1466
EP - 1474
JO - Arthritis and Rheumatology
JF - Arthritis and Rheumatology
IS - 9
ER -