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Antiphospholipid Antibodies and Recurrent Thrombotic Events: Persistence and Portfolio

机译:抗磷脂抗体和复发性血栓事件:持久性和产品组合。

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Background: There are very limited prospective data on the significance of persistent antiphospholipid antibodies (aPL) and recurrent thrombo-occlusive events (TOEs). We investigated the prognostic value of (1) 2 newer aPL assays, (2) an aPL portfolio and (3) persistent aPL positivity following stroke. Methods: A total of 1,770 subjects from the APASS-WARSS study underwent further aPL testing for antibodies to phosphatidylserine (aPS) and anti-beta(2)-glycoprotein-I (anti- beta(2) GPI) from stored sera. Follow-up aPL status was also tested in a subset of subjects. Primary analysis was based on time to any TOE (ischemic stroke, myocardial infarction, transient ischemic attack, deep vein thrombosis, pulmonary embolism or systemic arterial occlusion)/death at 2 years. Cox proportional hazard analyses assessed whether aPL independently related to outcome. Results: Persistent anti-beta(2) GPI decreased the time to TOE/death after adjustment for potential confounders (hazards ratio (HR) 2.86, 95% CI 1.21-6.76, p = 0.017). When persistent anti-beta(2) GPI was combined with another persistently positive aPL, time to TOE/death was also reduced (HR 3.79, 95% CI 1.18-12.14, p = 0.025). Neither persistent anticardiolipin antibodies nor persistent aPS alone nor a single positive anti-beta(2) GPI nor aPS was associated with decreased time to TOE/ death. No single positive aPL, portfolio of baseline aPL or any persistent aPL increased
机译:背景:关于持久性抗磷脂抗体(aPL)和复发性血栓闭塞事件(TOEs)的意义的前瞻性数据非常有限。我们调查了(1)2种较新的aPL测定,(2)aPL产品组合和(3)中风后持久性aPL阳性的预后价值。方法:来自APASS-WARSS研究的1770名受试者接受了进一步的aPL测试,以检测来自储存血清的磷脂酰丝氨酸(aPS)和抗β(2)-糖蛋白-I(抗β(2)GPI)抗体。还对部分受试者的随访aPL状态进行了测试。初步分析基于2年时发生任何TOE(缺血性中风,心肌梗塞,短暂性脑缺血发作,深静脉血栓形成,肺栓塞或全身动脉闭塞)/死亡的时间。考克斯比例风险分析评估了aPL是否与结果独立相关。结果:持久性抗beta(2)GPI减少了对潜在混杂因素进行调整后的TOE /死亡时间(危险比(HR)2.86,95%CI 1.21-6.76,p = 0.017)。当持久性抗β(2)GPI与另一种持久性阳性aPL结合使用时,到达TOE /死亡的时间也减少了(HR 3.79,95%CI 1.18-12.14,p = 0.025)。持久性抗心磷脂抗体,单独的持久性aPS或单独的阳性抗beta(2)GPI或aPS均与缩短TOE /死亡时间无关。没有单个积极的aPL,基准aPL的投资组合或任何持续的aPL增加

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