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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河南中医药大学

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] 国家中医药管理局中医优势专科外科建设项目(国中医药医政函(2024)90号)


Crosstalk Between Metabolic Reprogramming and Inflammatory Coagulation: Novel Targets for Intervening in Deep Vein Thrombosis
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Department of Peripheral Vascular,the First Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou

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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,并指出其中的治疗策略级面临的挑战,为DVT防治提供新路径。

    Abstract:

    Deep vein thrombosis (DVT) is the third most common cardiovascular disease in the world.Traditional anticoagulation therapy is limited. The pathophysiology of DVT usually focuses on Virchow triad, but it cannot explain many clinical problems, and the interaction between metabolic reprogramming and inflammation and coagulation may open up new perspectives for its theory. To explore the role of metabolic microenvironment in thrombosis and oxidative stress in metabolic reprogramming and thrombosis, analyze the feedback loop between metabolic reprogramming and inflammatory coagulation, summarize the therapeutic strategies of metabolic regulation intervention in DVT, including glucose metabolism, lipid metabolism intervention and antioxidant therapy, and point out the challenges faced by the therapeutic strategy level, providing a new way for the prevention and treatment of DVT.

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  • 收稿日期:2025-06-12
  • 最后修改日期:2025-09-16
  • 录用日期:2026-01-04
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