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塞尔维亚原发性抗磷脂综合征患者分析显示网状青斑与动脉血栓形成密切相关:一项全国性横断面队列研究。

Analysis of Serbian Primary Antiphospholipid Syndrome Patients Confirmed a Strong Association Between Livedo Reticularis and Arterial Thrombosis: A National Cross-Sectional Cohort Study.

机构信息

COVID Hospital Batajnica and Clinics of.

Urology.

出版信息

J Clin Rheumatol. 2022 Oct 1;28(7):362-366. doi: 10.1097/RHU.0000000000001879. Epub 2022 Jun 12.

Abstract

BACKGROUND

Antiphospholipid syndrome (APS) is characterized by antiphospholipid antibodies (aPLs) associated with thrombosis (arterial and/or venous) and/or obstetrical manifestations. However, various manifestations, which are considered to be noncriteria manifestations, are frequently found in APS.

AIM

The purpose of this study was to evaluate whether noncriteria manifestations may be found more frequently in subjects with thrombotic and/or obstetrical APS ("criteria" manifestations) in a population of patients with primary APS (PAPS). This study presents the results from our national cohort.

PATIENTS AND METHODS

This is a cross-sectional study of 360 PAPS patients. Data regarding the presence of thrombocytopenia, livedo reticularis, chorea, and valvulopathy were analyzed. The aPL analysis included the detection of anticardiolipin antibodies (aCLs: immunoglobulin G [IgG]/IgM), anti-β 2 glycoprotein I (IgG/IgM), and lupus anticoagulant positivity.

RESULTS

In our cohort, livedo reticularis was significantly related to arterial thromboses in the same way as valvular manifestations (valvular vegetations and valvular thickening and dysfunction not related to age) ( p = 0.0001, p = 0.013, respectively). Age was strongly related to all the noncriteria manifestations analyzed. Thrombocytopenia was significantly related to β 2 glycoprotein I IgG and lupus anticoagulant positivity ( p = 0.043, p = 0.030, respectively), as well as to double and triple aPL positivity ( p = 0.041, p = 0.013 respectively). Moreover, in a multivariate model, livedo reticularis was strongly and independently related to arterial thrombosis in our cohort (odds ratio, 2.010; confidence interval, 1.229-3.288; p = 0.005).

CONCLUSION

This cross-sectional analysis of a large cohort of Serbian PAPS patients confirmed a strong relationship between livedo reticularis and arterial thrombosis, suggesting a more cautious approach regarding the presence of noncriteria manifestations, especially livedo reticularis, in APS.

摘要

背景

抗磷脂综合征(APS)的特征是存在抗磷脂抗体(aPL)与血栓(动脉和/或静脉)和/或产科表现相关。然而,APS 中经常发现各种被认为是非标准表现的表现。

目的

本研究旨在评估在原发性 APS(PAPS)患者人群中,是否在具有血栓形成和/或产科 APS(“标准”表现)的患者中更频繁地发现非标准表现。本研究呈现了我们的全国队列研究结果。

患者和方法

这是一项针对 360 名 PAPS 患者的横断面研究。分析了血小板减少、网状青斑、舞蹈病和瓣膜病的数据。aPL 分析包括检测抗心磷脂抗体(aCL:IgG/IgM)、抗β2 糖蛋白 I(IgG/IgM)和狼疮抗凝剂阳性。

结果

在我们的队列中,网状青斑与动脉血栓形成的关系与瓣膜表现(瓣膜赘生物和与年龄无关的瓣膜增厚和功能障碍)相同(p=0.0001,p=0.013)。年龄与分析的所有非标准表现均有很强的相关性。血小板减少与β2 糖蛋白 I IgG 和狼疮抗凝剂阳性显著相关(p=0.043,p=0.030),以及双和三 aPL 阳性(p=0.041,p=0.013)。此外,在多变量模型中,网状青斑在我们的队列中与动脉血栓形成有很强的独立关系(比值比,2.010;95%置信区间,1.229-3.288;p=0.005)。

结论

对大量塞尔维亚 PAPS 患者的横断面分析证实,网状青斑与动脉血栓形成之间存在很强的关系,这表明在 APS 中,特别是网状青斑,存在非标准表现时应更加谨慎。

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