Improving diagnosis in patients with obstetric antiphospholipid syndrome through the evaluation of non-criteria antibodies

IF 4.6 2区 医学 Q2 IMMUNOLOGY Clinical & Translational Immunology Pub Date : 2024-12-13 DOI:10.1002/cti2.70021
Daniel Álvarez, Hephzibah E Winter, Carlos J Velasquez Franco, Aleida Susana Castellanos Gutierrez, Núria Baños, Udo R Markert, Ángela P Cadavid, Diana M Morales-Prieto
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Abstract

Objectives

Antiphospholipid syndrome (APS) is an autoimmune disease driven by antiphospholipid antibodies (aPL). Currently, APS diagnosis requires a combination of clinical manifestations (thrombosis and/or obstetric morbidity) and the persistent presence of at least one criteria aPL: anti-cardiolipin antibodies (aCL), anti-β2-glycoprotein I antibodies (aβ2GPI) or lupus anticoagulant (LA). Patients with suggestive obstetric symptoms but lacking criteria aPL face diagnostic challenges. Non-criteria aPL screening may enhance discrimination. This study proposes a classification incorporating both criteria and non-criteria antibodies to improve obstetric APS diagnosis.

Methods

Blood samples from non-pregnant women (n = 68) with a history of vascular, obstetric, or vascular and obstetric manifestations were analysed. Among them, 30 had previous diagnosis of APS. Healthy women with proven gestational success were included as controls (n = 16). Criteria and non-criteria (anti-phosphatidylglycerol, anti-phosphatidylethanolamine, anti-phosphatidylinositol, anti-phosphatidylserine and anti-phosphatidic acid) IgG aPL were evaluated by ELISA and coagulation tests. Based on the resulting aPL profile, patients were reclassified. Responsiveness to treatment was obtained from medical records.

Results

Criteria aPL levels marginally differentiated women previously managed as obstetric APS from unexplained/other causes of obstetric morbidity. Including non-criteria aPL improved separation. The proposed classification identified an obstetric APS group that exhibits non-criteria aPL and aβ2GPI titres below the cut-off but higher than healthy women (7.88 vs. 2.47 SGU, P = 0.006). Compared to cases of other causes of obstetric morbidity, these patients retrospectively responded better to aspirin and/or heparin treatment (71.43% vs. 11.11%, P = 0.035).

Conclusions

Assessing non-criteria antibodies may identify isolated obstetric APS cases benefiting from established therapies.

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通过评估非标准抗体提高产科抗磷脂综合征患者的诊断。
目的:抗磷脂综合征(APS)是一种由抗磷脂抗体(aPL)驱动的自身免疫性疾病。目前,APS的诊断需要结合临床表现(血栓形成和/或产科发病)和至少一种标准aPL的持续存在:抗心磷脂抗体(aCL)、抗β2-糖蛋白I抗体(a -β 2gpi)或狼疮抗凝剂(LA)。有暗示性产科症状但缺乏标准aPL的患者面临诊断挑战。非标准aPL筛查可能增强歧视。本研究提出了一种结合标准和非标准抗体的分类,以改善产科APS诊断。方法:对有血管、产科病史或血管和产科表现的非妊娠妇女(n = 68)的血液样本进行分析。其中30例既往诊断为APS。经证实妊娠成功的健康妇女作为对照组(n = 16)。采用ELISA和凝血试验评价标准和非标准(抗磷脂酰甘油、抗磷脂酰乙醇胺、抗磷脂酰肌醇、抗磷脂酰丝氨酸和抗磷脂酸)IgG aPL。根据结果的aPL谱,对患者进行重新分类。从医疗记录中获得对治疗的反应性。结果:标准aPL水平将以前作为产科APS管理的妇女与不明原因/其他原因的产科发病率区分开来。包括非标准api改善了分离。建议的分类确定了一个产科APS组,其显示非标准aPL和aβ2GPI滴度低于临界值,但高于健康妇女(7.88 vs 2.47 SGU, P = 0.006)。与其他原因的产科发病病例相比,这些患者对阿司匹林和/或肝素治疗的回顾性反应更好(71.43%比11.11%,P = 0.035)。结论:评估非标准抗体可以识别孤立的产科APS病例受益于既定的治疗。
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来源期刊
Clinical & Translational Immunology
Clinical & Translational Immunology Medicine-Immunology and Allergy
CiteScore
12.00
自引率
1.70%
发文量
77
审稿时长
13 weeks
期刊介绍: Clinical & Translational Immunology is an open access, fully peer-reviewed journal devoted to publishing cutting-edge advances in biomedical research for scientists and physicians. The Journal covers fields including cancer biology, cardiovascular research, gene therapy, immunology, vaccine development and disease pathogenesis and therapy at the earliest phases of investigation.
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