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抗磷脂抗体携带者的风险评估与抗栓策略

Risk Assessment and Antithrombotic Strategies in Antiphospholipid Antibody Carriers.

作者信息

Calcaterra Ilenia, Ambrosino Pasquale, Vitelli Nicoletta, Lupoli Roberta, Orsini Roberta Clara, Chiurazzi Martina, Maniscalco Mauro, Di Minno Matteo Nicola Dario

机构信息

Department of Clinical Medicine and Surgery, Faculty of Medicine and Surgery, Federico II University, 80131 Naples, Italy.

Istituti Clinici Scientifici Maugeri IRCCS, 27100 Pavia, Italy.

出版信息

Biomedicines. 2021 Jan 27;9(2):122. doi: 10.3390/biomedicines9020122.

DOI:10.3390/biomedicines9020122
PMID:33513790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7911177/
Abstract

Antiphospholipid antibodies (aPL) are a cluster of autoantibodies directed against plasma proteins with affinity for membrane phospholipids. The most frequently tested aPL are lupus anticoagulant (LA), anti-cardiolipin antibodies (aCL), and anti-β2-glycoprotein I antibodies (anti-β2GPI). aPL play a key pathogenic role in the development of the antiphospholipid syndrome (APS), a systemic autoimmune disease characterized by recurrent thrombotic and/or pregnancy complications in patients with persistent aPL. However, aPL positivity is occasionally documented in patients with no previous history of thrombotic or pregnancy morbidity. LA activity, multiple aPL positivity, high-titer aPL, and a concomitant systemic autoimmune disease are recognized risk factors for future thrombotic events in asymptomatic carriers. Moreover, an accelerated atherosclerosis with increased cardiovascular (CV) risk has also been associated with aPL positivity, thus exposing aPL carriers to fatal complications and chronic disability requiring cardiac rehabilitation. Overall, an accurate risk stratification is recommended for aPL-positive subjects in order to prevent both venous and arterial thrombotic complications. In this review, we provide an overview of the main antithrombotic and risk assessment strategies in aPL carriers.

摘要

抗磷脂抗体(aPL)是一类针对与膜磷脂具有亲和力的血浆蛋白的自身抗体。最常检测的aPL是狼疮抗凝物(LA)、抗心磷脂抗体(aCL)和抗β2糖蛋白I抗体(抗β2GPI)。aPL在抗磷脂综合征(APS)的发生发展中起关键致病作用,APS是一种系统性自身免疫性疾病,其特征是持续存在aPL的患者反复出现血栓形成和/或妊娠并发症。然而,既往无血栓形成或妊娠相关疾病史的患者偶尔也会出现aPL阳性。LA活性、多种aPL阳性、高滴度aPL以及合并系统性自身免疫性疾病是无症状携带者未来发生血栓事件的公认危险因素。此外,aPL阳性还与动脉粥样硬化加速及心血管(CV)风险增加有关,从而使aPL携带者面临致命并发症和需要心脏康复的慢性残疾风险。总体而言,建议对aPL阳性患者进行准确的风险分层,以预防静脉和动脉血栓并发症。在本综述中,我们概述了aPL携带者主要的抗血栓形成和风险评估策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9e8/7911177/1326da4a3337/biomedicines-09-00122-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9e8/7911177/46fb5d6386aa/biomedicines-09-00122-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9e8/7911177/1326da4a3337/biomedicines-09-00122-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9e8/7911177/46fb5d6386aa/biomedicines-09-00122-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9e8/7911177/1326da4a3337/biomedicines-09-00122-g002.jpg

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Blood Rev. 2021 Jul;48:100788. doi: 10.1016/j.blre.2020.100788. Epub 2020 Dec 13.
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Antiphospholipid patterns predict risk of thrombosis in systemic lupus erythematosus.抗磷脂抗体谱预测系统性红斑狼疮血栓形成风险。
Rheumatology (Oxford). 2021 Aug 2;60(8):3770-3777. doi: 10.1093/rheumatology/keaa857.
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Training intensity and improvements in exercise capacity in elderly patients undergoing European cardiac rehabilitation - the EU-CaRE multicenter cohort study.
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Insights into the Procoagulant Profile of Patients with Systemic Lupus Erythematosus without Antiphospholipid Antibodies.对无抗磷脂抗体的系统性红斑狼疮患者促凝特征的见解
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Antibody profiles comprising anti phosphatidylserine/prothrombin differently affect thrombin generation and protein C resistance in antiphospholipid antibody carriers.包含抗磷脂酰丝氨酸/凝血酶原的抗体谱对抗磷脂抗体携带者的凝血酶生成和蛋白C抵抗有不同影响。
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