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Critical Update of the Antiphospholipid Syndrome Criteria

机译:抗磷脂综合征标准的重要更新。

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Diagnosis of Antiphospholipid Syndrome (APS) is made when vascular thrombosis or pregnancy morbidity occur in patients with circulating antiphospholipid antibodies [lupus anticoagulant (LA) and/or IgG/IgM anticardiolipin (aCL) and/or IgG/IgM anti-β2glycoprotein I (aβ2GPI) antibodies]. Although each test may identify different autoantibodies, a single positive test makes the diagnosis possible when positive on two or more occasions at least 12 weeks apart. However, single test positivity may be unrelated to pathogenic antibodies that are now considered a subclass of aβ2GPI directed to Domain I of the protein. Conversely, all the test positive identify a single class of aβ2GPI antibodies and identify high risk patients with APS.
机译:当循环中的抗磷脂抗体[狼疮抗凝剂(LA)和/或IgG / IgM抗心磷脂(aCL)和/或IgG / IgM抗β2糖蛋白I(aβ2GPI)的患者发生血管血栓形成或妊娠合并症时,应进行抗磷脂综合症(APS)的诊断。 )抗体]。尽管每种测试可能会鉴定出不同的自身抗体,但如果两次或多次间隔至少12周呈阳性,则单个阳性测试可以使诊断成为可能。但是,单一测试阳性可能与致病性抗体无关,而致病性抗体现在被认为是针对蛋白质结构域I的aβ2GPI的亚类。相反,所有测试阳性的患者都可以识别一类aβ2GPI抗体,并可以识别高危的APS患者。

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