代谢重编程与炎症凝血的交互作用干预深静脉血栓形成的研究进展
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作者单位:

1.河南中医药大学第一附属医院周围血管科,郑州 450000;2.河南中医药大学第一临床医学院,郑州 450000

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R543. 6

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Crosstalk between metabolic reprogramming and inflammatory coagulation: novel targets for interventions in deep vein thrombosis
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Affiliation:

1. Department of Peripheral Vascular, the First Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou 450000, China. 2. the First Clinical School of Henan University of Chinese Medicine, Zhengzhou 450000

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    摘要:

    深静脉血栓形成(DVT)是全球第三大心血管疾病,传统抗凝治疗受限。 其病理生理学通常聚焦于 Virchow 三联征,但无法解释诸多临床问题,代谢重编程与炎症凝血的交互作用可能为其理论开拓了新角度。 本文阐述 DVT 中糖代谢、脂代谢异常的促栓机制,包括糖代谢对血小板的活化、内皮功能障碍等影响,脂代谢中他汀类药物的保护作用及脂代谢与血栓的风险关系。 同时探讨代谢微环境对血栓形成的作用,以及氧化应激在代谢重编程与血栓形成中的角色。 分析代谢重编程与炎症凝血反应的反馈环路,总结代谢调控干预 DVT 的治疗策略,包括糖代谢、脂代谢干预及抗氧化治疗,并指出其中治疗策略面临的挑战,为 DVT 防治提供新路径。

    Abstract:

    Deep vein thrombosis (DVT) is the third most common cardiovascular disease worldwide but traditional anticoagulation therapy options are limited. The pathophysiology of DVT usually focuses on Virchow’ s triad, but this fails to explain many of the clinical problems. Considering the interactions of metabolic reprogramming with inflammation and coagulation may thus open up new perspectives. This review explores the roles of the metabolic microenvironment in thrombosis and oxidative stress in relation to metabolic reprogramming and thrombosis, analyzes the feedback loop between metabolic reprogramming and inflammatory coagulation, and summarizes the therapeutic strategies of metabolic regulation intervention in DVT, including glucose metabolism, lipid metabolism, and antioxidant therapy. We also highlight the challenges in terms of therapeutic strategies, and indicate potential new approaches to the prevention and treatment of DVT.

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刘 成,周 涛.代谢重编程与炎症凝血的交互作用干预深静脉血栓形成的研究进展[J].中国比较医学杂志,2026,35(2):126~137.

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  • 收稿日期:2025-06-12
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  • 在线发布日期: 2025-05-06
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