Exploring the Mechanisms of Hypercoagulability in Thrombotic Antiphospholipid Syndrome: A Scoping Review of Human Studies.

IF 4.1 2区 医学 Q2 HEMATOLOGY
Sigrid Elvira Dam Østergaard, Rasmus Søgaard Hansen, Anne Voss, Mustafa Vakur Bor
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Abstract

Thrombosis is the most common manifestation of antiphospholipid syndrome (APS), but concurring evidence of the mechanisms leading to a hypercoagulable state and thereby thrombosis is lacking. Existing reviews on this topic often include both animal and in vitro models. Additionally, studies with a systematic approach and stringent methodology, focusing exclusively on human studies, are lacking. Therefore, we conducted a scoping review of studies with human subjects, focusing on the mechanisms contributing to hypercoagulability in thrombotic APS (T-APS). The process was guided by the PRISMA Extension for Scoping Reviews and performed according to a preregistered protocol in Open Science Framework (https://osf.io/tjdwv). A systematic search of Ovid (EMBASE) and MEDLINE (PubMed) was performed on October 10, 2024. Records investigating mechanisms of hypercoagulability in adults (≥18 years) with T-APS, published between January 2000 and October 2024, were included. A total of 4,160 titles and abstracts were screened, 115 articles were assessed in full text, of which 35 studies fulfilled the predefined eligibility criteria for inclusion. Of the included studies, 8 focused on primary hemostasis, 10 on secondary hemostasis, 9 on fibrinolysis, 4 on neutrophil extracellular traps, 6 on endothelial cells, 3 on complement factors, 5 on monocytes, 3 on oxidized low-density lipoprotein complexes, 2 on oxidative stress, and 1 on amyloid-β1-40. No clear consensus was found regarding the underlying cause of hypercoagulability in T-APS, highlighting the need for further studies with human subjects. Nonetheless, this scoping review indicates that hypercoagulability in T-APS is possibly multifactorial, with no single mechanism being solely responsible.

探索血栓性抗磷脂综合征的高凝机制:对人类研究的范围综述。
血栓形成是抗磷脂综合征(APS)最常见的表现,但缺乏导致高凝状态从而形成血栓的机制的一致证据。关于这一主题的现有评论,通常包括动物和体外模型。此外,缺乏专门针对人体研究的系统方法和严格方法的研究。因此,我们对人类受试者的研究进行了范围审查,重点关注血栓性APS中高凝性的机制。该过程由Prisma Extension进行范围审查指导,并根据开放科学框架(https://osf.io/tjdwv)中预先注册的协议进行。于2024年10月10日对Ovid (EMBASE)和MEDLINE (PubMed)进行系统检索。在2000年1月至2024年10月期间发表的研究成人(18岁)血栓性APS高凝机制的记录。共筛选了4160篇标题和摘要,对115篇文章进行了全文评估,其中35篇研究符合预定的纳入资格标准。在纳入的研究中,8项针对原发性止血,10项针对继发性止血,9项针对纤维蛋白溶解,4项针对中性粒细胞胞外陷阱,6项针对内皮细胞,3项针对补体因子,5项针对单核细胞,3项针对氧化LDL复合物,2项针对氧化应激,1项针对淀粉样蛋白- β -40。关于血栓性APS高凝性的潜在原因,没有明确的共识,强调需要进一步的人类受试者研究。尽管如此,这一范围综述表明血栓性APS的高凝性可能是多因素的,没有单一的机制单独负责。
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来源期刊
Seminars in thrombosis and hemostasis
Seminars in thrombosis and hemostasis 医学-外周血管病
CiteScore
8.80
自引率
21.10%
发文量
132
审稿时长
6-12 weeks
期刊介绍: Seminars in Thrombosis and Hemostasis is a topic driven review journal that focuses on all issues relating to hemostatic and thrombotic disorders. As one of the premiere review journals in the field, Seminars in Thrombosis and Hemostasis serves as a comprehensive forum for important advances in clinical and laboratory diagnosis and therapeutic interventions. The journal also publishes peer reviewed original research papers. Seminars offers an informed perspective on today''s pivotal issues, including hemophilia A & B, thrombophilia, gene therapy, venous and arterial thrombosis, von Willebrand disease, vascular disorders and thromboembolic diseases. Attention is also given to the latest developments in pharmaceutical drugs along with treatment and current management techniques. The journal also frequently publishes sponsored supplements to further highlight emerging trends in the field.
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