Kitagawa Yasuhisa
Department of Neurology, Tokai University Hachioji Hospital.
Rinsho Shinkeigaku. 2005 Nov;45(11):852-5.
Antiphospholipid syndrome is characterized by arterial or venous thrombosis, and the presence of antiphospholipid antibodies (aPL). APL are considered to be a cause of an acquired hypercoagulable state leading to stroke and transient ischemic attack (TIA). We examined the causes in 50 young patients with ischemic stroke. The most prevalent cause was atherosclerosis and the incidence of APS was 12.5%. APL comprise a heterogeneous group of autoantibodies, such as beta2-glycoprotein I dependent anticardiolipin antibody (beta2-GPIaCL), lupus anticoagulant (LA), and other antiphospholid-protein antibodies. We examined the incidence and the pathogenic role of antiphospholipid protein antibodies. The subjects comprised 250 patients (155 male, 95 females) with ischemic stroke, aged 26 to 92 years (mean 72 years). We measured beta2-GPI aCL, IgG aCL, LA, phosphatidyserine dependent antiprothrtombin antibody (PS-PT), antiphosphatidyl-serine antibody (PS), antiphosphatidyl-inositol antibody (PI) in each patient. The incidence of beta2-GPI aCL, IgG aCL, LA, phosphatidyserine, PS-PT, PS, and PI was 2.8%, 12%, 9.2%, 7.2%, 9.6%, and 8.8%, respectively. The incidence of young stroke patients under 50 years was 5.2%. Among 13 young stroke patients, 5 had SLE. Among 23 patients with LA., 18 (78%) patients had PS-PT. Anti-PS-PT antibody is closely related to LA. Antinuclear antibody was detected in 79% of the patients with aPS and/or aPI. We compared the carotid ultrasonographic findings in positive aPI or aPS patients with those in negative ones. Increased IMT, plaque score and carotid stenosis were more common in aPI and aPS-positive patients than in negative ones Three of 5 patients who showed positive beta2-GPI, aCL and LA, simulataneously, had sysyemic lupus erythematosus as an immulological background. Two of 3 patients with PI and/or PS and beta2-GPI and/or LA were patients with SLE. Antiphospholipid antibody was considered to be a risk factor of stroke, especially in SLE and/or young female patients. The incidence of lupus anticoagulant is more common than beta2-GPI aCL in ischemic stroke. In SLE patients with stroke, multi-antiphospholipid-protein antibodies was inclined to be present. LA is closely related to ant-PS-PT and aPI and aPS are associated with anti-nuclear antibody and precipitation of atherosclerosis.
抗磷脂综合征的特征为动脉或静脉血栓形成以及抗磷脂抗体(aPL)的存在。抗磷脂抗体被认为是导致获得性高凝状态从而引发中风和短暂性脑缺血发作(TIA)的一个原因。我们研究了50例年轻缺血性中风患者的病因。最常见的病因是动脉粥样硬化,抗磷脂综合征的发病率为12.5%。抗磷脂抗体包括一组异质性自身抗体,如β2糖蛋白I依赖性抗心磷脂抗体(β2-GPIaCL)、狼疮抗凝物(LA)以及其他抗磷脂蛋白抗体。我们研究了抗磷脂蛋白抗体的发病率及其致病作用。研究对象包括250例缺血性中风患者(男性155例,女性95例),年龄在26至92岁之间(平均72岁)。我们检测了每位患者的β2-GPI aCL、IgG aCL、LA、磷脂酰丝氨酸依赖性抗凝血酶原抗体(PS-PT)、抗磷脂酰丝氨酸抗体(PS)、抗磷脂酰肌醇抗体(PI)。β2-GPI aCL、IgG aCL、LA、磷脂酰丝氨酸、PS-PT、PS和PI的发病率分别为2.8%、12%、9.2%、7.2%、9.6%和8.8%。50岁以下年轻中风患者的发病率为5.2%。在13例年轻中风患者中,5例患有系统性红斑狼疮(SLE)。在23例狼疮抗凝物阳性患者中,18例(78%)患者存在PS-PT。抗PS-PT抗体与狼疮抗凝物密切相关。在抗磷脂综合征和/或抗磷脂酰肌醇抗体阳性的患者中,79%检测到抗核抗体。我们比较了抗磷脂酰肌醇抗体或抗磷脂酰丝氨酸抗体阳性患者与阴性患者的颈动脉超声检查结果。内膜中层厚度增加、斑块评分和颈动脉狭窄在抗磷脂酰肌醇抗体和抗磷脂酰丝氨酸抗体阳性患者中比在阴性患者中更常见。同时出现β2-GPI、aCL和LA阳性的5例患者中有3例以系统性红斑狼疮作为免疫背景。3例抗磷脂酰肌醇和/或抗磷脂酰丝氨酸抗体以及β2-GPI和/或狼疮抗凝物阳性的患者中有2例患有系统性红斑狼疮。抗磷脂抗体被认为是中风的一个危险因素,尤其是在系统性红斑狼疮患者和/或年轻女性患者中。在缺血性中风中,狼疮抗凝物的发病率比β2-GPI aCL更常见。在中风的系统性红斑狼疮患者中,多抗磷脂蛋白抗体更容易出现。狼疮抗凝物与抗PS-PT密切相关,抗磷脂酰肌醇抗体和抗磷脂酰丝氨酸抗体与抗核抗体以及动脉粥样硬化的形成有关。