Mechanism of sickle cell disease-specific venous thromboembolism

镰状细胞病特异性静脉血栓栓塞的机制

基本信息

  • 批准号:
    10381739
  • 负责人:
  • 金额:
    $ 66.1万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-04-01 至 2025-03-31
  • 项目状态:
    未结题

项目摘要

Program Director/Principal Investigator (Last, First, Middle) Pawlinski, Rafal and Key, Nigel Abstract Venous thromboembolism (VTE) is the third most common form of cardiovascular disease after myocardial infarction and ischemic stroke, with approximately 900,000 cases annually in the United States. VTE may present clinically as deep vein thrombosis (DVT) and/or pulmonary embolism (PE). However, it is unknown why some patients present with symptomatic DVT, while others present with PE. In recent years, it has been established that individuals with sickle cell disease (SCD), as well as carriers for SCD -- who are said to have sickle cell trait -- are at increased risk of VTE. Interestingly and unusually, in both sickle cell disease and trait, a skewed distribution in the proportions of patients with DVT and PE (in favor of PE) is observed. We have termed this phenomenon “the sickle cell paradox”. SCD is due to an inherited mutation in hemoglobin that is expressed exclusively in red blood cells (RBCs). Therefore, in this proposal, we postulate that a greater understanding of the mechanism of VTE in SCD, as well as an explanation for the sickle cell paradox, will be explained by a detailed study of the role of sickle RBCs in VTE. To address this question, we will utilize animal models of SCD with experimentally induced venous thrombi, while concurrently studying the qualitative aspects of blood clots formed from the blood of patients with SCD ex vivo. Towards this goal, we will address the following specific aims: in Aim 1, we will determine the effect of RBCs on venous thromboembolism in a mouse model of SCD. We expect that partial RBC exchange will result in smaller, more stable DVTs and a reduced incidence of PE. In Aim 2, we will investigate how sickle RBCs enhance thrombin generation in SCD. In the third Aim, we will determine the cellular and molecular mechanisms that attenuate sensitivity of sickle clots to fibrinolysis. We anticipate this effect is mediated both by the inherited defect in SCD RBCs, but also the fact that platelets in patients with SCD are over-activated. Finally, in Aim 4, we will determine whether reduction of platelet numbers reduces VTE and restores normal susceptibility to fibrinolysis in sickle mice and SCD patients undergoing chronic RBC exchange. With an annual worldwide SCD birth rate of more than 300,000 (and an estimated 250 million individuals with sickle trait), a greater mechanistic understanding of VTE in sickle cell disorders is a high priority. OMB No. 0925-0001/0002 (Rev. 03/16 Approved Through 10/31/2018) Page Continuation Format Page
项目主管/首席研究员(最后,第一,中间)Pawlinski, Rafal和Key, Nigel

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Nigel S. Key其他文献

Validation of Townes As Mice As a Model of Chronic Kidney Disease and Venous Thrombosis Associated with Sickle Cell Trait
  • DOI:
    10.1182/blood-2023-186635
  • 发表时间:
    2023-11-02
  • 期刊:
  • 影响因子:
  • 作者:
    Malgorzata Kasztan;Steven P Grover;Fatima Trebak;Mohammad O Sako;Nigel S. Key;Rafal Pawlinski
  • 通讯作者:
    Rafal Pawlinski
Adults with Severe or Moderately Severe Hemophilia B Receiving Etranacogene Dezaparvovec in the HOPE-B Phase 3 Clinical Trial Continue to Experience a Stable Increase in Mean Factor IX Activity Levels and Durable Hemostatic Protection after 24 Months’ Follow-up
  • DOI:
    10.1182/blood-2022-166135
  • 发表时间:
    2022-11-15
  • 期刊:
  • 影响因子:
  • 作者:
    Steven W. Pipe;Frank W.G. Leebeek;Michael Recht;Nigel S. Key;Susan Lattimore;Giancarlo Castaman;Michiel Coppens;David Cooper;Robert Gut;Sergio Slawka;Stephanie Verweij;Ricardo Dolmetsch;Yanyan Li;Paul E. Monahan;Wolfgang A. Miesbach
  • 通讯作者:
    Wolfgang A. Miesbach
Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency
导致异常剪接和因子 V 缺乏的明显同义 F5 突变的表征
  • DOI:
  • 发表时间:
    2015
  • 期刊:
  • 影响因子:
    3.9
  • 作者:
    F. Nuzzo;C. Bulato;B. Nielsen;Kristy Lee;Simone J.H. Wielders;Paolo Simioni;Nigel S. Key;E. Castoldi
  • 通讯作者:
    E. Castoldi
78: Variant Hemoglobin May Affect Erythropoietin Response in African-Americans Receiving Hemodialysis
  • DOI:
    10.1053/j.ajkd.2010.02.085
  • 发表时间:
    2010-04-01
  • 期刊:
  • 影响因子:
  • 作者:
    Vimal K. Derebail;Patrick H. Nachman;Nigel S. Key;Heather Ansede;Ronald J. Falk;Abhijit V. Kshirsagar
  • 通讯作者:
    Abhijit V. Kshirsagar

Nigel S. Key的其他文献

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{{ truncateString('Nigel S. Key', 18)}}的其他基金

Mechanism of sickle cell disease-specific venous thromboembolism
镰状细胞病特异性静脉血栓栓塞的机制
  • 批准号:
    10611915
  • 财政年份:
    2021
  • 资助金额:
    $ 66.1万
  • 项目类别:
Mechanism of sickle cell disease-specific venous thromboembolism
镰状细胞病特异性静脉血栓栓塞的机制
  • 批准号:
    10184626
  • 财政年份:
    2021
  • 资助金额:
    $ 66.1万
  • 项目类别:
Mechanisms of Venous Thromboembolism in Cancer
癌症静脉血栓栓塞的机制
  • 批准号:
    8307478
  • 财政年份:
    2008
  • 资助金额:
    $ 66.1万
  • 项目类别:
Mechanisms of Venous Thromboembolism in Cancer
癌症静脉血栓栓塞的机制
  • 批准号:
    8117261
  • 财政年份:
    2008
  • 资助金额:
    $ 66.1万
  • 项目类别:
Mechanisms of Venous Thromboembolism in Cancer
癌症静脉血栓栓塞的机制
  • 批准号:
    7904072
  • 财政年份:
    2008
  • 资助金额:
    $ 66.1万
  • 项目类别:
Mechanisms of Venous Thromboembolism in Cancer
癌症静脉血栓栓塞的机制
  • 批准号:
    8403088
  • 财政年份:
    2008
  • 资助金额:
    $ 66.1万
  • 项目类别:
Mechanisms of Venous Thromboembolism in Cancer
癌症静脉血栓栓塞的机制
  • 批准号:
    7691277
  • 财政年份:
    2008
  • 资助金额:
    $ 66.1万
  • 项目类别:
Catheter Directed Thrombolytic Therapy in Deep Vein Thrombosis
深静脉血栓的导管定向溶栓治疗
  • 批准号:
    7041961
  • 财政年份:
    2003
  • 资助金额:
    $ 66.1万
  • 项目类别:
PREVENT: Prevention of Recurrent Venous Thromboembolism
预防:预防复发性静脉血栓栓塞
  • 批准号:
    7041926
  • 财政年份:
    2003
  • 资助金额:
    $ 66.1万
  • 项目类别:
Tissue factor in hemophilia
血友病中的组织因子
  • 批准号:
    6642372
  • 财政年份:
    2002
  • 资助金额:
    $ 66.1万
  • 项目类别:

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