新生血管性年龄相关性黄斑变性的黄斑萎缩

E. Selim, M. Selim
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引用次数: 7

摘要

据估计,全球有近1000万人患有高龄相关性黄斑变性(AMD)。晚期AMD与高龄、吸烟、阳性家族史、遗传易感性、高脂肪摄入和肥胖有关。据预测,从2020年到2040年,晚期黄斑变性的患病率将增加约65%这一增长的很大一部分将以新生血管性年龄相关性黄斑变性的形式出现,从2020年到2040年,其患病率可能增加约47%。在工业化国家,年龄相关性黄斑变性仍然是50岁以上人群视力丧失的主要原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macular atrophy in neovascular age related macular degeneration
Advanced age related macular degeneration (AMD) is estimated to affect nearly 10 million people worldwide. Late AMD is associated with advancing age, smoking, positive family history, genetic susceptibility, high fat intake and obesity.1–4 It is predicted for advanced macular degeneration to increase in prevalence from the year 2020 to year 2040 by about 65%.1 A large percentage of that increase will be in the form of neovascular age related macular degeneration which is likely to increase in prevalence by about 47% from the year 2020 to the year 2040.2 Age related macular degeneration remains the leading cause of visual loss in people above 50 years old in industrialized countries.
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