Author/Editor     Avčin, T; Ambrožič, A; Božič, B; Accetto, M; Kveder, T; Rozman, B
Title     Estimation of anticardiolipin antibodies, anti-beta2glycoprotein I antibodies and lupus anticoagulant in a prospective longitudinal study of children with juvenile idiopathic arthritis
Type     članek
Source     Clin Exp Rheumatol
Vol. and No.     Letnik 20, št. 1
Publication year     2002
Volume     str. 101-8
Language     eng
Abstract     Anticardiolipin antibodies (aCL) have been frequently detected in juvenile idiopathic arthritis (JIA), but have not been associated with disease activity or clinical features of the antiphospholipid syndrome (APS). Our aim was to determine aCL and anti-beta2 glycoprotein 1(anti-l32GPl) antibody levels and lupus anticoagulant (LA) in serial samples from children with JIA and to investigate the clinical significance of these antibodies. Methods The values of aCL, anti-beta2GPI and LA were prospectively followed in 28 children with JIA from disease onset. aCL and anti-/32GP1 were assayed by an ELISA method. Two monoclonal beta2GPI-dependent aCL (HCAL and EY2C9) were used as calibrators. LA was determined by a modifed dilute Russell viper venom time test. Results Thirteen (46.4%) children with JIA were already positive for aCL at their first referral to our center. During the followup, the frequency of aCL decreased from 46.4% to 28.6%; however, it remained significantly higher compared with healthy children. In contrast, for anti-l3zGPl the difference in the frequency between the children with JIA and healthy children was not statistically significant. Serial determination of aPL levels in JIA patients revealed frequent fluctuations. Positive aCL persisted over time in 6 (21.4%) children with JIA, 6 (21.4%) children were initially positive for aCL, but became later negative, and 3 (10.7%) children were initially negative for aCL and became later positive. Persistently positive anti-beta2GPl were observed during the follow-up only in one patient, while none of the patients was persistently positive for LA. No association between aCL, anti-beta2GP1 or LA and disease activity could be established. No patient with positive aCL, anti-l32GPI or LA showed any clinical feature of APS. (Abstract truncated at 2000 characters).
Descriptors     ARTHRITIS, JUVENILE RHEUMATOID
ANTIBODIES, ANTICARDIOLIPIN
ANTIBODIES, ANTIPHOSPHOLIPID
LUPUS COAGULATION INHIBITOR