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ADVANCED GLYCATION ENDPRODUCTS: BIOMARKERS FOR AGE-RELATED MACULAR DEGENERATION

机译:先进的糖化封闭剂:生物标志物,用于年龄相关的黄斑变性

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Age-related macular degeneration (AMD) is a complex, progressive disease involving multiple genetic and environmental factors and a major cause of severe visual loss in the elderly worldwide. Deposition of debris (drusen) along Bruch's membrane in the macula (Figure 1) is the first evidence of early AMD. Advanced AMD occurs in two forms, geographic atrophy and choroidal neovascularization. Geographic atrophy (advanced dry AMD) develops slowly and results in blindness when focal areas of the retinal pigment epithelium (RPE) degenerate in the macula. Choroidal neovascularization (wet AMD) is characterized by the growth of new blood vessels from the choroid through Bruch's membrane and the RPE. When these vessels hemorrhage, a blood clot accumulates between the RPE and the macular photoreceptors, causing immediate central vision loss. Wet AMD accounts for over 80% of debilitating visual loss in AMD yet only 10-15% of AMD cases progress to neovascular AMD.
机译:与年龄相关的黄斑变性(AMD)是一种复杂,渐进的疾病,涉及多种遗传和环境因素,以及全球老年人严重视力损失的主要原因。 在黄斑中沿着Bruch的膜沉积(图1)是早期AMD的第一个证据。 先进的AMD以两种形式,地理萎缩和脉络膜新生血管形成发生。 地理萎缩(晚期干燥AMD)慢慢发展,并在黄斑中退化的视网膜颜料上皮(RPE)的焦点区域时盲目。 脉络膜新生血管(湿AMD)的特征在于通过BRUCH的膜和RPE从脉络膜中生长新的血管。 当这些血管出血时,血凝块累积在RPE和黄斑光感受器之间,导致即时中央视力丧失。 湿法占AMD衰弱的80%以上的80%,但只有10-15%的AMD病例进展到新血管AMD。

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