德鲁森
医学
黄斑变性
阿柏西普
血管抑制剂
血管内皮生长因子
眼科
哌加他尼
脉络膜新生血管
生物信息学
病理
肿瘤科
贝伐单抗
内科学
生物
化疗
血管内皮生长因子受体
作者
Paul Mitchell,Gerald Liew,Bamini Gopinath,Tien Yin Wong
出处
期刊:The Lancet
[Elsevier]
日期:2018-09-01
卷期号:392 (10153): 1147-1159
被引量:1101
标识
DOI:10.1016/s0140-6736(18)31550-2
摘要
Summary
Age-related macular degeneration is a leading cause of visual impairment and severe vision loss. Clinically, it is classified as early-stage (medium-sized drusen and retinal pigmentary changes) to late-stage (neovascular and atrophic). Age-related macular degeneration is a multifactorial disorder, with dysregulation in the complement, lipid, angiogenic, inflammatory, and extracellular matrix pathways implicated in its pathogenesis. More than 50 genetic susceptibility loci have been identified, of which the most important are in the CFH and ARMS2 genes. The major non-genetic risk factors are smoking and low dietary intake of antioxidants (zinc and carotenoids). Progression from early-stage to late-stage disease can be slowed with high-dose zinc and antioxidant vitamin supplements. Intravitreal anti-vascular endothelial growth factor therapy (eg, ranibizumab, aflibercept, or bevacizumab) is highly effective at treating neovascular age-related macular degeneration, and has markedly decreased the prevalence of visual impairment in populations worldwide. Currently, no proven therapies for atrophic disease are available, but several agents are being investigated in clinical trials. Future progress is likely to be from improved efforts in prevention and risk-factor modification, personalised medicine targeting specific pathways, newer anti-vascular endothelial growth factor agents or other agents, and regenerative therapies.
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