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IgG anti-beta2-glycoprotein I antibodies in adult patients with systemic lupus erythematosus: prevalence and diagnostic value for the antiphospholipid syndrome. The Journal of rheumatology. [J Rheumatol] Journal article

 
TitleIgG anti-beta2-glycoprotein I antibodies in adult patients with systemic lupus erythematosus: prevalence and diagnostic value for the antiphospholipid syndrome.
Author(s)Tubach F, Hayem G, Marchand JL, Weber M, Palazzo E, de Bandt M, Roux S, Kahn MF, Meyer O 
InstitutionDepartment of Rheumatology, Bichat Teaching Hospital, University of Paris, France.
SourceJ Rheumatol 2000 Jun; 27(6):1437-43.
MeSHAdolescent
Adult
Aged
Antibodies, Anticardiolipin
Biological Markers
Child
Female
Glycoproteins
Humans
Immunoglobulin G
Lupus Coagulation Inhibitor
Lupus Erythematosus, Systemic
Male
Middle Aged
Predictive Value of Tests
Risk Factors
Seroepidemiologic Studies
Thrombosis
AbstractOBJECTIVE: To investigate the prevalence of serum anti-beta2-glycoprotein I (anti-beta2-GPI) antibodies and other antiphospholipid antibodies (aPL) in patients with systemic lupus erythematosus (SLE). To study their diagnostic value for the antiphospholipid syndrome (APS).
METHODS: Anti-beta2-GPI and IgG anticardiolipin (aCL) were determined in sera from 102 consecutive patients with SLE using ELISA. Serum and plasma tests were also done for lupus anticoagulant (LAC), syphilis, and antibodies to dsDNA. Clinical and laboratory features of APS were observed.
RESULTS: Prevalences were 23.5% for aCL and 18.6% for anti-beta2-GPI. Correlations between the presence of aCL and anti-beta2-GPI and between their titers were statistically significant (p<0.0001). No associations were found between anti-beta2-GPI and disease activity criteria (SLEDAI, ECLAM, dsDNA). Anti-beta2-GPI were significantly associated with LAC (p = 0.005), APS (p = 0.005), and a high aCL titer (aCL > 5 SD; p< or =0.001). LAC was the best diagnostic criterion for APS.
CONCLUSION: These data suggest that determination of anti-beta2-GPI in addition to aCL and LAC is unlikely to improve the diagnosis of APS in patients with SLE.
Languageeng
Pub Type(s)Journal Article
PubMed ID10852267
  
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