Recent Updates on the Diagnosis and Management of Age-Related Macular Degeneration

Nithya Boopathiraj MBBS , Isabella V. Wagner BS , Syril K. Dorairaj MD , Darby D. Miller MD , Michael W. Stewart MD
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Abstract

Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in the Western world, with a higher prevalence among Europeans and North Americans than that in Africans, Hispanics, and Asians. Advanced AMD is categorized as atrophic (dry) or exudative (wet/neovascular age-related macular degeneration [nAMD]). Dry AMD is characterized by progressive geographic atrophy of the retinal pigment epithelium and outer retinal layers, whereas nAMD is characterized by new vessels that invade the subretinal and/or subretinal pigment epithelium spaces. Existing treatments delay the onset of advanced AMD and reverses vision loss for a couple of years before atrophy usually decreases central visual acuity. We searched PubMed and Medline databases from January 1, 1980, to December 1, 2023, using the following search terms: macular degeneration, choroidal neovascularization, geographic atrophy, drusen, age-related maculopathy, AMD, ARMD, and anti-VEGF. Relevant articles in English (or English translations) were retrieved and reviewed. Bibliographies of the identified manuscripts were also reviewed to identify relevant studies. Age-related macular degeneration most commonly affects people older than 55 years. Visual prognosis varies, with advanced lesions (nAMD and geographic atrophy) leading to rapid, progressive loss of central vision and contrast sensitivity. Although AMD is not a life-threatening disease, reduced vision profoundly compromises quality of life and necessitates living assistance for many patients. Over the past 2 decades, advances in prevention (vitamin supplementation) and therapy (antivascular endothelial growth factor and complement inhibitor drugs) have reduced vision loss and blindness. Further research is needed to decrease the incidence of blindness in patients with advanced disease.

老年性黄斑变性诊断和管理的最新进展
老年性黄斑变性(AMD)是西方世界导致不可逆性失明的主要原因,在欧洲人和北美人中的发病率高于非洲人、西班牙裔人和亚洲人。晚期黄斑变性分为萎缩性(干性)和渗出性(湿性/新血管性年龄相关性黄斑变性[nAMD])。干性黄斑变性的特征是视网膜色素上皮和视网膜外层的进行性地理萎缩,而湿性黄斑变性的特征是新血管侵入视网膜下和/或视网膜下色素上皮间隙。现有的治疗方法可延缓晚期 AMD 的发生,并在萎缩通常导致中心视力下降之前的几年内逆转视力下降。我们检索了1980年1月1日至2023年12月1日期间的PubMed和Medline数据库,检索词包括:黄斑变性、脉络膜新生血管、地理萎缩、色素沉着、年龄相关性黄斑病、AMD、ARMD和抗血管内皮生长因子。检索并审查了相关的英文(或英文翻译)文章。此外,还查阅了已确定稿件的书目,以确定相关研究。年龄相关性黄斑变性最常影响 55 岁以上的人群。视力预后各不相同,晚期病变(nAMD 和地域性萎缩)会导致中心视力和对比敏感度的快速、渐进性丧失。虽然老年性视力减退症不会危及生命,但视力下降会严重影响生活质量,许多患者需要生活援助。在过去的 20 年中,预防(补充维生素)和治疗(抗血管内皮生长因子和补体抑制剂药物)方面的进步减少了视力下降和失明。要降低晚期患者的失明率,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mayo Clinic proceedings. Innovations, quality & outcomes
Mayo Clinic proceedings. Innovations, quality & outcomes Surgery, Critical Care and Intensive Care Medicine, Public Health and Health Policy
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