产科抗磷脂综合征:从发病机理到治疗。

IF 2.7 Q3 IMMUNOLOGY
Immunological Medicine Pub Date : 2022-06-01 Epub Date: 2021-09-01 DOI:10.1080/25785826.2021.1969116
Kayoko Kaneko, Nobuaki Ozawa, Atsuko Murashima
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引用次数: 6

摘要

抗磷脂综合征(APS)是一种自身免疫性疾病,其临床表现为血栓形成和产科并发症,并伴有抗磷脂抗体(APS)的持续存在。最近的研究表明,apl相关的产科并发症的原因是apl引起的胎盘滋养细胞功能障碍和母胎界面炎症,而不是血栓形成。尽管apl与妊娠期间严重并发症的复发有关,但肝素和低剂量阿司匹林的适当联合治疗可改善70-80%的妊娠进程。孕前咨询和患者量身定制的治疗是改善孕产妇和胎儿结局的基础。非抗凝治疗,如羟氯喹和他汀类药物正在开发,以治疗传统治疗难治性的病例。通过对大型产科APS数据库的分析,确定妊娠并发症后血栓形成的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obstetric anti-phospholipid syndrome: from pathogenesis to treatment.

Antiphospholipid syndrome (APS) is an autoimmune disease characterized by clinical manifestations such as thrombosis and obstetric complications with documented persistence of antiphospholipid antibodies (aPLs). Recent studies have revealed that the cause of aPL-related obstetric complications is dysfunction of placental trophoblasts and inflammation of the maternal-fetal interface induced by aPLs, not thrombosis. Although aPLs are associated with recurrence of serious complications during pregnancy, appropriate combination therapy with heparin and low-dose aspirin can improve the course of 70-80% of subsequent pregnancies. Preconception counseling and patient-tailored treatment are fundamental to improving maternal and fetal outcomes. Non-anticoagulant treatments such as hydroxychloroquine and statins are being developed for cases refractory to conventional treatment. Risk factors for thrombosis after pregnancy complications were identified based on the analysis of large databases of obstetric APS.

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来源期刊
Immunological Medicine
Immunological Medicine Medicine-Immunology and Allergy
CiteScore
7.10
自引率
2.30%
发文量
19
审稿时长
19 weeks
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