Avcin Tadej, Benseler Susanne M, Tyrrell Pascal N, Cucnik Sasa, Silverman Earl D
The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Arthritis Rheum. 2008 Feb 15;59(2):206-13. doi: 10.1002/art.23334.
To determine the prevalence of anticardiolipin antibodies (aCL), anti-beta(2)-glycoprotein I (anti-beta(2)GPI) antibodies, and lupus anticoagulant (LAC) in a large cohort of children with systemic lupus erythematosus (SLE), and to evaluate the associations with neuropsychiatric manifestations.
A single-center retrospective cohort study with longitudinal followup of antiphospholipid antibodies (aPL) in 137 children with SLE (25 boys and 112 girls, mean age at diagnosis 13.0 years) was performed. Patients were followed up for a mean of 31 months.
At the time of diagnosis, 65% of the children were aCL positive, 41% had anti-beta(2)GPI antibodies, and 26% were LAC positive. Analysis of the association between presence of aPL and individual neuropsychiatric manifestations at diagnosis showed a statistically significant association of positive LAC with cerebrovascular disease (5 patients; P = 0.015). A persistently positive aCL was observed in 50%, anti-beta(2)GPI antibodies in 29%, and LAC in 16% of children over time. The prevalence of anti-beta(2)GPI antibodies, but not aCL and LAC, was found to be statistically significantly higher in children with neuropsychiatric disease compared with those without (P = 0.02). Comparison for specific neuropsychiatric manifestations showed a statistically significant association between a persistently positive LAC and chorea (2 patients; P = 0.02).
The prevalence of anti-beta(2)GPI antibodies was found to be higher in the group of SLE patients with neuropsychiatric disease compared with those without. Our data suggest an association between LAC and cerebrovascular disease at the time of SLE diagnosis and chorea over the disease course, but not between aPL and other neuropsychiatric manifestations.
确定一大群系统性红斑狼疮(SLE)患儿中抗心磷脂抗体(aCL)、抗β2糖蛋白I抗体(抗β2GPI)和狼疮抗凝物(LAC)的患病率,并评估其与神经精神症状的相关性。
对137例SLE患儿(25例男孩和112例女孩,诊断时平均年龄13.0岁)进行了一项单中心回顾性队列研究,并对其抗磷脂抗体(aPL)进行纵向随访。患者平均随访31个月。
诊断时,65%的患儿aCL呈阳性,41%有抗β2GPI抗体,26% LAC呈阳性。对诊断时aPL的存在与个体神经精神症状之间的相关性分析显示,LAC阳性与脑血管疾病之间存在统计学显著相关性(5例患者;P = 0.015)。随着时间的推移,50%的患儿aCL持续呈阳性,29%的患儿抗β2GPI抗体持续呈阳性,16%的患儿LAC持续呈阳性。与无神经精神疾病的患儿相比,神经精神疾病患儿中抗β2GPI抗体的患病率在统计学上显著更高(P = 0.02),而aCL和LAC则不然。对特定神经精神症状的比较显示,LAC持续阳性与舞蹈症之间存在统计学显著相关性(2例患者;P = 0.02)。
与无神经精神疾病的SLE患者相比,有神经精神疾病的SLE患者组中抗β2GPI抗体的患病率更高。我们的数据表明,在SLE诊断时LAC与脑血管疾病以及在疾病过程中LAC与舞蹈症之间存在关联,但aPL与其他神经精神症状之间无关联。