Mody Sankalp, Joshi Abhishek
Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences, Wardha, IND.
Community Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences, Wardha, IND.
Cureus. 2023 Feb 13;15(2):e34920. doi: 10.7759/cureus.34920. eCollection 2023 Feb.
Age-related macular degeneration (AMD) is a highly prevalent macular condition that primarily affects the older population. It is the primary cause of blindness amongst the elderly population. It is an inflammatory disease that characteristically shows choroidal neovascularization and geographic atrophy. The exact pathomechanism of developing AMD is not known. However, certain factors such as increased age, smoking, genetic factors and certain environmental factors are usually associated with the development of the disease. AMD also involves oxidative stress-mediated destruction of retinal pigment epithelial cells and, consequently, that of retinal photoreceptors. Alzheimer's disease (AD) is a degenerative disorder involving the nervous system that usually affects people aged 65 and over. Both AMD and AD are age-related, degenerative conditions that have several similarities and share many of the same risk factors such as vascular conditions like arteriosclerosis, high blood pressure and obesity. It is believed that the early emergence of the clinical manifestations of AMD and AD may also be significantly influenced by oxidative stress and genetic polymorphism in complement factor H. A common pathogenic pathway between AD and AMD is quite likely. Amyloid-β is an aberrant protein that accumulates within the brains of Alzheimer's patients and appears as plaques on magnetic resonance imaging (MRI). These plaques are a pathognomonic sign of Alzheimer's disease. Similar to this, amyloid-β deposits are reported to build up beneath the retina of AMD patients, which appear as tiny clusters of protein-lipid substances known as drusen. It has also been found that individuals suffering from AMD exhibit an increased chance of developing AD than those with no AMD.
年龄相关性黄斑变性(AMD)是一种高度常见的黄斑疾病,主要影响老年人群。它是老年人群失明的主要原因。这是一种炎症性疾病,其特征表现为脉络膜新生血管形成和地图样萎缩。AMD的确切发病机制尚不清楚。然而,某些因素,如年龄增长、吸烟、遗传因素和某些环境因素,通常与该疾病的发生有关。AMD还涉及氧化应激介导的视网膜色素上皮细胞破坏,进而导致视网膜光感受器的破坏。阿尔茨海默病(AD)是一种累及神经系统的退行性疾病,通常影响65岁及以上的人群。AMD和AD都是与年龄相关的退行性疾病,它们有一些相似之处,并且共享许多相同的风险因素,如动脉硬化、高血压和肥胖等血管疾病。据信,AMD和AD临床表现的早期出现也可能受到氧化应激和补体因子H基因多态性的显著影响。AD和AMD之间很可能存在共同的致病途径。淀粉样β蛋白是一种异常蛋白质,在阿尔茨海默病患者的大脑中积聚,并在磁共振成像(MRI)上表现为斑块。这些斑块是阿尔茨海默病的特征性标志。与此类似,据报道,淀粉样β蛋白沉积物在AMD患者的视网膜下积聚,表现为称为玻璃膜疣的微小蛋白质-脂质物质簇。还发现,与没有AMD的人相比,患有AMD的个体患AD的几率增加。