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抗磷脂综合征的实验室诊断。

Laboratory Diagnostics of Antiphospholipid Syndrome.

机构信息

Department of Cardiac Thoracic and Vascular Sciences, Clinical Cardiology, Thrombosis Centre, University of Padova, Padova, Italy.

出版信息

Semin Thromb Hemost. 2018 Jul;44(5):439-444. doi: 10.1055/s-0037-1601331. Epub 2017 May 3.

Abstract

Diagnosis of antiphospholipid syndrome (APS) lies in the recognition of antiphospholipid antibodies (aPL). As standardization of tests for the detection of aPL is far from being optimal and reference material is not available, inappropriate diagnoses of APS are not unusual. In the last few years, the concept of triple test positivity has emerged as a useful tool to identify patients with APS. Clinical studies on patients and carriers of triple positivity clearly show that these individuals are at high risk of thromboembolic events and pregnancy loss. Moreover, triple positivity arises from a single (probably pathogenic) antibody directed to domain 1 of β-glycoprotein I, a protein whose function is still unknown. Studies on homogenous group of patients with single or double positivity are scant, and uncertainties arise on their association with clinical events. Promising but undetermined results come also from the determination of antibodies directed to phosphatidylserine/prothrombin complex. Interpretation of laboratory profile in APS is challenging, and the collaboration between clinical pathologists and clinicians is highly desirable.

摘要

抗磷脂综合征(APS)的诊断在于识别抗磷脂抗体(aPL)。由于检测 aPL 的检测标准化远非最佳,且没有参考材料,因此不适当的 APS 诊断并不罕见。在过去几年中,三联检测阳性的概念已成为识别 APS 患者的有用工具。对三联阳性患者和携带者的临床研究清楚地表明,这些个体有发生血栓栓塞事件和妊娠丢失的高风险。此外,三联阳性来自针对β-糖蛋白 I 结构域 1 的单一(可能是致病性的)抗体,该蛋白的功能尚不清楚。关于具有单一或双重阳性的同质患者组的研究很少,并且它们与临床事件的关联存在不确定性。来自针对磷脂酰丝氨酸/凝血酶原复合物的抗体的测定也有希望但尚未确定的结果。APS 中的实验室谱的解释具有挑战性,临床病理学家和临床医生之间的合作是非常需要的。

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