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Blood, 15 December 2005, Vol. 106, No. 13, pp. 4152-4158.
Prepublished online as a Blood First Edition Paper on September 6, 2005; DOI 10.1182/blood-2005-05-2048.
Previous Article | Next Article 
Submitted May 23, 2005
Accepted July 29, 2005
Predictive value of persistent versus transient antiphospholipid antibody subtypes for the risk of thrombotic events in pediatric patients with systemic lupus erythematosus
Christoph Male, Denise Foulon, Hugh Hoogendoorn, Patricia Vegh, Earl Silverman, Michele David, and Lesley Mitchell*
Children's Hospital, Medical University of Vienna, Vienna, Austria; Henderson Research Centre, McMaster University, Hamilton, Ontario, Canada
Henderson Research Centre, McMaster University, Hamilton, Ontario, Canada
Hospital for Sick Children, Toronto, Ontario, Canada
Hospital Ste. Justine, Montreal, Quebec, Canada
Stollery Children's Hospital, Edmonton, Alberta, Canada
* Corresponding author; email: lesleymitchell{at}cha.ab.ca.
Study objectives were to determine in children with systemic lupus erythematosus (SLE) the: i) association of antiphosholipid antibody (APLA) subtypes with thrombotic events (TE); ii) predictive value of persistent versus transient antibodies for TE. Cohort study of 58 SLE children in whom lupus anticoagulants (LA), anticardiolipin antibodies (ACLA), anti- 2-glycoprotein-I (anti- 2GPI), anti-prothrombin (anti-PT) were assessed on 2 occasions ( >3 months apart). Antibodies were classified as persistent (positive 2 occasions) or transient (positive once). Outcomes were symptomatic TE, confirmed by objective radiographic tests identified retrospectively and prospectively.
Seven of 58 patients (12%) had 10 TE; 5 patients had TE during prospective follow-up. Persistent LA showed the strongest association with TE (p< 0.0001). Persistent ACLA (p=0.003) and anti- 2GPI (p=0.002) were significantly associated with TE, anti-PT (p=0.063) showed a trend. Persistent or transient LA and anti- 2GPI showed similar strength of association, while ACLA and anti-PT were no longer associated with TE. Positivity for multiple APLA subtypes showed stronger associations with TE than for individual APLA subtypes because of improved specificity.
Lupus anticoagulant is the strongest predictor of the risk of TE, other APLA subtypes provide no additional diagnostic value. Anticardiolipin antibodies and anti-PT require serial testing, as only persistent antibodies are associated with TE.

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