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血友病患者出血倾向和关节病发展的异质性。

Heterogeneity in Bleeding Tendency and Arthropathy Development in Individuals with Hemophilia.

机构信息

Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, Dublin, Ireland.

National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.

出版信息

Semin Thromb Hemost. 2021 Mar;47(2):183-191. doi: 10.1055/s-0041-1723769. Epub 2021 Feb 26.

Abstract

People with hemophilia (PWH) have an increased tendency to bleed, often into their joints, causing debilitating joint disease if left untreated. To reduce the incidence of bleeding events, PWH receive prophylactic replacement therapy with recombinant factor VIII (FVIII) or FIX. Bleeding events in PWH are typically proportional to their plasma FVIII or IX levels; however, in many PWH, bleeding tendency and the likelihood of developing arthropathy often varies independently of endogenous factor levels. Consequently, many PWH suffer repeated bleeding events before correct dosing of replacement factor can be established. Diagnostic approaches to define an individual's bleeding tendency remain limited. Multiple modulators of bleeding phenotype in PWH have been proposed, including the type of disease-causing variant, age of onset of bleeding episodes, plasma modifiers of blood coagulation or clot fibrinolysis pathway activity, interindividual differences in platelet reactivity, and endothelial anticoagulant activity. In this review, we summarize current knowledge of established factors modulating bleeding tendency and discuss emerging concepts of additional biological elements that may contribute to variable bleeding tendency in PWH. Finally, we consider how variance in responses to new gene therapies may also necessitate consideration of patient-specific tailoring of treatment. Cumulatively, these studies highlight the need to reconsider the current "one size fits all" approach to treatment regimens for PWH and consider therapies guided by the bleeding phenotype of each individual PWH at the onset of therapy. Further characterization of the biological bases of bleeding heterogeneity in PWH, combined with the development of novel diagnostic assays to identify those factors that modulate bleeding risk in PWH, will be required to meet these aspirations.

摘要

患有血友病(PWH)的人出血倾向增加,经常出血到关节,如果不治疗,会导致关节疾病。为了减少出血事件的发生,PWH 接受重组凝血因子 VIII(FVIII)或 FIX 的预防性替代治疗。PWH 的出血事件通常与他们的血浆 FVIII 或 IX 水平成正比;然而,在许多 PWH 中,出血倾向和发生关节病的可能性往往独立于内源性因子水平。因此,许多 PWH 在确定替代因子的正确剂量之前会经历反复出血事件。用于定义个体出血倾向的诊断方法仍然有限。已经提出了 PWH 出血表型的多种调节剂,包括致病变异的类型、出血发作的年龄、血液凝固或血栓纤溶途径活性的血浆调节剂、个体间血小板反应性的差异以及内皮抗凝活性。在这篇综述中,我们总结了目前关于调节出血倾向的既定因素的知识,并讨论了可能导致 PWH 出血倾向变化的新兴生物学因素的概念。最后,我们考虑了新基因治疗的反应差异如何也可能需要考虑根据每个 PWH 的出血表型对治疗方案进行个体化调整。综上所述,这些研究强调需要重新考虑目前针对 PWH 的“一刀切”治疗方案,并考虑在治疗开始时根据每个 PWH 的出血表型指导治疗的疗法。进一步阐明 PWH 出血异质性的生物学基础,并开发用于识别调节 PWH 出血风险的因素的新型诊断检测,将是实现这些目标所必需的。

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