[关键词]
[摘要]
视网膜中央静脉阻塞(CRVO)是致盲性视网膜血管疾病,其机制涉及多系统交互作用。文章系统综述CRVO病理机制,聚焦血管内皮功能障碍、动脉硬化、易栓症、炎症及氧化应激等核心环节。其病理机制包括动脉硬化通过机械压迫和内皮素-1介导收缩双重机制阻碍静脉回流; 内皮功能异常加剧血流紊乱; 遗传性和获得性凝血异常破坏凝血稳态,促进血栓形成; 炎症与氧化应激协同激活细胞因子,加重缺血和血管渗漏。文章创新性探讨了外泌体通过miRNA递送调控血管功能,肠道菌群失衡经“肠-眼轴”代谢通路影响视网膜微环境,进而通过多维度机制网络解析,阐明CRVO从局部病变到全身代谢紊乱的病理关联,强调眼-全身协同干预的重要性。本综述为疾病早期诊断标志物筛选、多靶点药物研发及个体化治疗提供理论依据,推动CRVO诊疗向整合医学模式转化。
[Key word]
[Abstract]
Central retinal vein occlusion(CRVO)is a retinal vascular disorder that significantly impairs vision, with its underlying mechanisms involving complex interactions across multiple biological systems. This article provides a systematic review of the pathological mechanisms associated with CRVO, emphasizing critical factors such as endothelial dysfunction, arteriosclerosis, thrombophilia, inflammation, and oxidative stress. The pathological mechanisms of CRVO are characterized by arteriosclerosis, which obstructs venous return through a dual mechanism involving mechanical compression and endothelin-1-mediated contraction; endothelial dysfunction, which exacerbates disturbances in blood flow; genetic and acquired coagulation abnormalities that disrupt hemostatic balance and promote thrombosis; and the synergistic effects of inflammation and oxidative stress that activate cytokines, thereby aggravating ischemia and vascular leakage. Innovatively, this review explores emerging mechanisms such as miRNA-mediated vascular regulation via exosomes, gut microbiota-retina crosstalk through the “gut-eye axis,” and systemic metabolic interactions that link local retinal lesions to broader dysregulation of CRVO. These insights underscore the importance of integrated eye-system interventions and provide a theoretical foundation for advancing early biomarker discovery, multitarget therapeutics, and personalized treatment paradigms. By bridging localized pathology and systemic mechanisms, this work promotes a transformative shift toward an integrative medicine model in the diagnosis and management of CRVO.
[中图分类号]
[基金项目]
山东省医药卫生科技项目(No.202303011346)