评估疑似抗磷脂综合征患者的频率、临床相关性和抗体确认谱。

Filipe F Martins, Teresa M L Campos
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引用次数: 1

摘要

抗磷脂综合征(APS)是一种系统性自身免疫性疾病,以持续抗磷脂(aPL)抗体患者的动脉和静脉血栓形成表现和/或妊娠相关并发症为特征。札幌的分类标准的引入使得这种病理的分类统一,在诊断方面取得了相当大的进步。然而,目前对这些标准的适用仍然存在一些疑问。本研究的目的是通过评估aPL患病率、临床和实验室检查之间的关联以及评估aPL确诊性特征来更好地了解APS。在这项研究中,我们分析了1179份来自疑似APS患者的样本,这些患者不分性别,没有年龄限制,被建议检测完整的aPL特征。检测狼疮抗凝血剂(LAC)、抗心磷脂免疫球蛋白(Ig) G/IgM和抗β-2-糖蛋白I IgG/IgM抗体。有单独检测要求分析的患者样本和受抗凝剂影响或处于感染过程的患者样本被排除在外。总阳性率为17.9%,最常见的aPL为LAC。抗体分别进行了分离和联合检测。三检阳性率为0.8%,双检阳性率为1.8%。与门诊服务相比,住院/急诊服务的阳性率更高。41岁以上、男性、系统性红斑狼疮、肾脏并发症和深静脉血栓/血栓性静脉炎患者的阳性率较高。第二份样本的阳性确认率为39.5%,阳性确认率为50.6%;17.3%的样本具有不同的特征,在这些样本中,2.5%的样本证实具有与先前检测到的不同的抗体。这项研究表明,aPL的阳性倾向于随着年龄的增长而增加,这表明在急性事件期间应避免检测aPL,并加强了在第二次样本和随后的检测中对完整aPL实验室资料的需求。
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Evaluation of Frequency, Clinical Correlation, and Antibodies Confirmation Profile in Patients with Suspected Antiphospholipid Syndrome.

Antiphospholipid syndrome (APS) is a systemic autoimmune disease characterized by arterial and venous thrombotic manifestations and/or pregnancy-related complications in patients with persistent antiphospholipid (aPL) antibodies. The introduction of Sapporo's classification criteria allowed uniformity in the classification of this pathology, representing a considerable advance in its diagnosis. However, currently some doubts about the application of these criteria still persist. The aim of this study was to contribute to the better understanding of APS by the assessment of aPL prevalence, the association between clinical and laboratory tests, and evaluation of the aPL confirmatory profile. In this study, 1,179 samples from patients with suspected APS of both genders, without age restrictions, who were advised to test for complete aPL's profile were analyzed. The samples were tested for lupus anticoagulant (LAC), anticardiolipin immunoglobulin (Ig) G/IgM and anti-β-2-glycoprotein I IgG/IgM antibodies. Patient samples with isolated test requests for analysis and samples from patients under the influence of anticoagulants or in an infectious process were excluded. The overall positivity found was 17.9% and the most frequent aPL was LAC. The antibodies were determined in isolation and in association. The prevalence of triple positivity was 0.8% and double positivity was 1.8%. Positivity was higher in inpatient/emergency services compared with outpatient services. There was a higher positivity in individuals over 41 years, males, patients with systemic lupus erythematosus, kidney complications, and deep vein thrombosis/thrombophlebitis. The positivity confirmation with second sample was 39.5% and the confirmation profile shows that 50.6% of samples confirmed with same positivity profile; 17.3% with a different profile and regarding to these, 2.5% of the samples confirmed positivity with a different antibody from the previously detected. This study suggests that the aPL's positivity tends to increase with age, showing that the aPL's testing should be avoided during an acute event and reinforces the need for complete aPL laboratory profile in the second sample and subsequent determinations.

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