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缓解期急性白血病患者巩固化疗期间血浆凝血因子 XIII 减少。

Reduced plasma coagulation factor XIII in patients with acute leukemia in remission during consolidation chemotherapy cycles.

机构信息

Department of Hematology, The First Hospital of Lanzhou University, Lanzhou, Gansu Province, China.

Department of Hematology and Oncology, Honghui Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi Province, China.

出版信息

Ann Hematol. 2023 Jul;102(7):1739-1744. doi: 10.1007/s00277-023-05261-y. Epub 2023 May 9.

DOI:10.1007/s00277-023-05261-y
PMID:37160793
Abstract

Acute leukemia (AL) is a malignancy from hematologic stem cells (HSC). Consolidation with intensive chemotherapy is required after induced remission and repeatedly causes treatment-related bleeding that is usually attributed to chemotherapy-induced thrombocytopenia (CIT). However, our previous study demonstrated that severe deficiency of plasma coagulation factor XIII (pFXIII) also participated in the bleeding of CIT in AL. However, the relationship between pFXIII deficiency and consolidation chemotherapy was unknown. Here, we observed the concentration of pFXIII in patients with AL before and after consolidation chemotherapy and reevaluated the correlation to bleeding in myelosuppression. Thus, we found that the concentration of pFXIII before chemotherapy in all patients was markedly lower than in the control data and was further decreased by chemotherapy, related to bleeding in myelosuppression. These findings indicated that chemotherapy-induced pFXIII deficiency should be of concern and explored in depth.

摘要

急性白血病 (AL) 是一种源于造血干细胞 (HSC) 的恶性肿瘤。在诱导缓解后需要进行强化化疗巩固,这会导致与治疗相关的出血,通常归因于化疗引起的血小板减少症 (CIT)。然而,我们之前的研究表明,血浆凝血因子 XIII (pFXIII) 的严重缺乏也参与了 AL 中 CIT 的出血。然而,pFXIII 缺乏与巩固化疗之间的关系尚不清楚。在这里,我们观察了接受巩固化疗前后 AL 患者的 pFXIII 浓度,并重新评估了其与骨髓抑制性出血的相关性。因此,我们发现所有患者化疗前的 pFXIII 浓度明显低于对照数据,且化疗后进一步降低,与骨髓抑制性出血相关。这些发现表明,化疗诱导的 pFXIII 缺乏应该引起关注并深入研究。

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Ann Hematol. 2023 Jul;102(7):1739-1744. doi: 10.1007/s00277-023-05261-y. Epub 2023 May 9.
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本文引用的文献

1
Sustained depletion of FXIII-A by inducing acquired FXIII-B deficiency.通过诱导获得性 FXIII-B 缺乏来持续耗尽 FXIII-A。
Blood. 2020 Dec 17;136(25):2946-2954. doi: 10.1182/blood.2020004976.
2
[Reduction of FXIII during myelosuppression in acute leukemia after chemotherapy and adverse relation with bleeding events].[化疗后急性白血病骨髓抑制期间因子 XIII 的降低及其与出血事件的不良关系]
Zhonghua Xue Ye Xue Za Zhi. 2020 Jan 14;41(1):59-63. doi: 10.3760/cma.j.issn.0253-2727.2020.01.011.
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通过血栓弹力图评估纤维蛋白原和因子 XIII 对血小板减少症和血小板无力症模型中凝血病的纠正作用。
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Minimal factor XIII activity level to prevent major spontaneous bleeds.预防自发性大出血的最小因子 XIII 活性水平。
J Thromb Haemost. 2017 Sep;15(9):1728-1736. doi: 10.1111/jth.13772. Epub 2017 Aug 17.
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Laboratory predictors of bleeding and the effect of platelet and RBC transfusions on bleeding outcomes in the PLADO trial.PLADO试验中出血的实验室预测指标以及血小板和红细胞输注对出血结局的影响。
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Cre/lox Studies Identify Resident Macrophages as the Major Source of Circulating Coagulation Factor XIII-A.Cre/lox研究确定组织驻留巨噬细胞是循环凝血因子XIII-A的主要来源。
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7
Factor XIII: Structure and Function.凝血因子 XIII:结构与功能
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Platelets but not monocytes contribute to the plasma levels of factor XIII subunit A in patients undergoing autologous peripheral blood stem cell transplantation.在接受自体外周血干细胞移植的患者中,血小板而非单核细胞对血浆中凝血因子 XIII A 亚基水平有影响。
Blood Coagul Fibrinolysis. 2004 Apr;15(3):249-53. doi: 10.1097/00001721-200404000-00009.
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Coagulation factor XIII A and B subunits in bone marrow and liver transplantation.骨髓和肝移植中的凝血因子XIII A亚基和B亚基
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