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The role of proteases and inflammatory molecules in triggering neovascular age-related macular degeneration: Basic science to clinical relevance

机译:蛋白酶和炎性分子在引发新生血管性年龄相关性黄斑变性中的作用:与临床相关的基础科学

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摘要

Age-related macular degeneration (AMD) causes severe vision impairment in aged individuals. The health impact and cost of the disease will dramatically increase over the years, with the increase in the aging population. Currently, antivascular endothelial growth factor agents are routinely used for managing late-stage AMD, and recent data have shown that up to 15%-33% of patients do not respond to this treatment. Henceforth, there is a need to develop better treatment options. One avenue is to investigate the role proteases and inflammatory molecules might have in regulating and being regulated by vascular endothelial growth factor. Moreover, emerging data indicate that proteases and inflammatory molecules might be critical in the development and progression of AMD. This article reviews recent literature that investigates proteases and inflammatory molecules involved in the development of AMD. Gaining insights into the proteolytic and inflammatory pathways associated with the pathophysiology of AMD could enable the development of additional or alternative drug strategies for the treatment of AMD.
机译:年龄相关性黄斑变性(AMD)会导致老年个体严重视力障碍。随着人口老龄化的增加,多年来对疾病的健康影响和代价将大大增加。当前,抗血管内皮生长因子药物通常用于晚期AMD的治疗,最近的数据表明,高达15%-33%的患者对此治疗无效。今后,有必要开发更好的治疗选择。一种途径是研究蛋白酶和炎性分子可能在血管内皮生长因子的调控中所起的作用。此外,新兴数据表明蛋白酶和炎性分子可能对AMD的发展和进程至关重要。本文回顾了研究涉及AMD发育的蛋白酶和炎性分子的最新文献。深入了解与AMD病理生理学相关的蛋白水解和炎症途径,可以开发出其他或替代药物来治疗AMD。

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