Venous Thrombosis Unchained: Pandora's Box of Non-Inflammatory Mechanisms.

IF 7.4 1区 医学 Q1 HEMATOLOGY
Sophie Robyn Megan Smith, Neil V Morgan, Alexander Brill
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引用次数: 0

Abstract

Venous thromboembolism (VTE), which includes deep vein thrombosis (DVT) and pulmonary embolism (PE), represents a complex pathological process extending far beyond inflammatory mechanisms. This review comprehensively examines the multifaceted non-inflammatory mechanisms underlying thrombosis development, integrating insights from molecular, physiological, and systemic levels. Blood flow dynamics and endothelial function are known to be critical regulators of thrombus development. Platelets and microparticles play important roles beyond conventional inflammatory responses, actively contributing to thrombus formation through intricate molecular interactions. Metabolic syndrome and insulin resistance are associated with thrombotic risk, demonstrating the complex interplay between metabolic disorders and DVT. Certain genetic mutations also predispose individuals to venous thrombosis. Emerging research has discovered the essential role of previously underappreciated factors such as products of gut microbiota or endothelial glycocalyx modifications. Molecular regulators such as microRNAs and hormonal disbalance further illustrate the complex mechanisms of venous thrombosis. Interestingly, circadian rhythms exhibit certain influence on thrombotic potential, introducing chronobiology as emerging variable affecting the risk of thrombosis. Based on these insights, future therapeutic strategies may include various interventions targeting or at least considering metabolic, molecular, and systemic non-inflammatory factors. Potential approaches include personalized risk stratification, microbiome modulation, endothelial protection approaches, and chronotherapy-based therapeutic modalities, that would ensure promising more efficient and safe thrombosis management.

静脉血栓释放:非炎症机制的潘多拉盒子。
静脉血栓栓塞(VTE)包括深静脉血栓形成(DVT)和肺栓塞(PE),是一个复杂的病理过程,远远超出了炎症机制。这篇综述全面探讨了血栓形成的多方面非炎症机制,整合了分子、生理和系统水平的见解。血流动力学和内皮功能被认为是血栓形成的关键调节因子。血小板和微粒在传统炎症反应之外发挥重要作用,通过复杂的分子相互作用积极促进血栓形成。代谢综合征和胰岛素抵抗与血栓形成风险相关,表明代谢紊乱与深静脉血栓形成之间存在复杂的相互作用。某些基因突变也使个体易患静脉血栓。新兴的研究已经发现了以前被低估的因素的重要作用,如肠道微生物群的产物或内皮糖萼修饰。分子调控因子如microrna和激素失衡进一步说明了静脉血栓形成的复杂机制。有趣的是,昼夜节律对血栓形成潜力有一定的影响,这使得时间生物学成为影响血栓形成风险的新变量。基于这些见解,未来的治疗策略可能包括针对或至少考虑代谢、分子和全身性非炎症因子的各种干预措施。潜在的方法包括个性化风险分层、微生物组调节、内皮保护方法和基于时间疗法的治疗方式,这些方法将确保更有效和安全的血栓管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Blood advances
Blood advances Medicine-Hematology
CiteScore
12.70
自引率
2.70%
发文量
840
期刊介绍: Blood Advances, a semimonthly medical journal published by the American Society of Hematology, marks the first addition to the Blood family in 70 years. This peer-reviewed, online-only, open-access journal was launched under the leadership of founding editor-in-chief Robert Negrin, MD, from Stanford University Medical Center in Stanford, CA, with its inaugural issue released on November 29, 2016. Blood Advances serves as an international platform for original articles detailing basic laboratory, translational, and clinical investigations in hematology. The journal comprehensively covers all aspects of hematology, including disorders of leukocytes (both benign and malignant), erythrocytes, platelets, hemostatic mechanisms, vascular biology, immunology, and hematologic oncology. Each article undergoes a rigorous peer-review process, with selection based on the originality of the findings, the high quality of the work presented, and the clarity of the presentation.
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