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疑似抗磷脂综合征患者的频率、临床相关性及抗体确认情况评估

Evaluation of Frequency, Clinical Correlation, and Antibodies Confirmation Profile in Patients with Suspected Antiphospholipid Syndrome.

作者信息

Martins Filipe F, Campos Teresa M L

机构信息

Department of Immunohemotherapy, Tâmega e Sousa Hospital Center, Penafiel, Portugal.

出版信息

TH Open. 2021 Oct 19;5(4):e470-e478. doi: 10.1055/s-0041-1736289. eCollection 2021 Oct.

Abstract

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.

摘要

抗磷脂综合征(APS)是一种全身性自身免疫性疾病,其特征为持续存在抗磷脂(aPL)抗体的患者出现动脉和静脉血栓形成表现及/或与妊娠相关的并发症。札幌分类标准的引入使该疾病的分类得以统一,这在其诊断方面是一项重大进展。然而,目前对于这些标准的应用仍存在一些疑问。本研究的目的是通过评估aPL的患病率、临床与实验室检查之间的关联以及评估aPL确证谱,来促进对APS的更好理解。在本研究中,分析了1179例来自疑似APS患者的样本,这些患者不限性别、年龄,均被建议检测完整的aPL谱。对样本进行狼疮抗凝物(LAC)、抗心磷脂免疫球蛋白(Ig)G/IgM以及抗β2糖蛋白I IgG/IgM抗体检测。排除仅要求进行分析检测的患者样本以及受抗凝剂影响或处于感染过程中的患者样本。总体阳性率为17.9%,最常见的aPL是LAC。分别及联合检测抗体。三联阳性的患病率为0.8%,双阳性为1.8%。住院/急诊患者的阳性率高于门诊患者。41岁以上个体、男性、系统性红斑狼疮患者、有肾脏并发症以及深静脉血栓形成/血栓性静脉炎患者的阳性率较高。第二次样本的阳性确认率为39.5%,确证谱显示50.6%的样本具有相同的阳性谱;17.3%具有不同的谱,其中2.5%的样本通过与先前检测不同的抗体确认阳性。本研究表明,aPL的阳性率倾向于随年龄增加,提示在急性事件期间应避免检测aPL,并强调在第二次样本及后续检测中需要完整的aPL实验室谱。

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