儿童同种异体造血干细胞移植后,移植物抗宿主病维持凝血活性两年。

IF 2.3 4区 医学 Q2 HEMATOLOGY
Satu Långström, Minna Koskenvuo, Pasi Huttunen, Riitta Lassila, Mervi Taskinen, Susanna Ranta, Markku Heikinheimo, Anne Mäkipernaa
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引用次数: 0

摘要

目的:评价小儿恶性血液病患者同种异体造血干细胞移植(HSCT)后的纵向凝血情况。方法:在30例儿科患者造血干细胞移植后两年的预定时间点测量几个凝血变量。结果:在造血干细胞移植后6个月,内皮细胞激活反映为循环血管性血癌因子活性增加1.4倍(p)。结论:接受造血干细胞移植的儿科患者表现出凝血系统的长期紊乱,在造血干细胞移植后6个月出现新的缓解平衡。然而,在cGVHD患者中,特别是当cGVHD影响胃肠道时,持续的凝血功能紊乱提示其在cGVHD和相关并发症中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graft-Versus-Host Disease Sustains Coagulation Activity for two Years After Pediatric Allogeneic Hematopoietic Stem Cell Transplantation.

Aim: To evaluate the longitudinal coagulation profile after allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients with hematological malignancies.

Methods: Several coagulation variables were measured at predetermined time points for two years after HSCT in 30 pediatric patients.

Results: At six months post-HSCT, endothelial activation was reflected by 1.4-fold increase in circulating von Willebrand factor activity (p < 0.05), and by 2-fold increase in thrombin-antithrombin complex levels (p < 0.05), suggesting sustained coagulation system activity. In six patients with chronic graft-versus-host disease (cGVHD), specifically in those having gastrointestinal (GI) tract cGVHD, we observed continued longitudinal alterations in the coagulation system. The activities of both, coagulation factors (FV, FVII, FVIII, fibrinogen), and natural anticoagulants (antithrombin and protein C) were higher than prior to conditioning (p < 0.05) at most time points in patients with cGVHD. Moreover, fibrin turnover marker D-dimer was elevated from 6 to 18 months after HSCT (p < 0.05).

Conclusion: Pediatric patients undergoing HSCT demonstrate prolonged derangement of the coagulation system, with a new alleviating balance after 6 months post-HSCT. However, in patients with cGVHD, and in particular when cGVHD affects the GI tract, the persisting derangement of coagulation suggest its contributing role in cGVHD and related complications.

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来源期刊
CiteScore
4.40
自引率
3.40%
发文量
150
审稿时长
2 months
期刊介绍: CATH is a peer-reviewed bi-monthly journal that addresses the practical clinical and laboratory issues involved in managing bleeding and clotting disorders, especially those related to thrombosis, hemostasis, and vascular disorders. CATH covers clinical trials, studies on etiology, pathophysiology, diagnosis and treatment of thrombohemorrhagic disorders.
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