John A. Moran Eye Center, University of Utah Health, Salt Lake City.
Department of Ophthalmology, University of Bonn, Bonn, Germany.
JAMA. 2024 Jan 9;331(2):147-157. doi: 10.1001/jama.2023.26074.
Age-related macular degeneration (AMD) affects approximately 20 million people in the US and 196 million people worldwide. AMD is a leading cause of severe vision impairment in older people and is expected to affect approximately 288 million people worldwide by 2040.
Older age, genetic factors, and environmental factors, such as cigarette smoking, are associated with development of AMD. AMD occurs when extracellular deposits accumulate in the outer retina, ultimately leading to photoreceptor degeneration and loss of central vision. The late stages of AMD are characterized by outer retinal atrophy, termed geographic atrophy, or neovascularization associated with subretinal and/or intraretinal exudation, termed exudative neovascular AMD. The annual incidence of AMD ranges from 0.3 per 1000 in people who are aged 55 to 59 years to 36.7 per 1000 in people aged 90 years or older. The estimated heritability of late-stage AMD is approximately 71% (95% CI, 18%-88%). Long-term prospective cohort studies show a significantly higher AMD incidence in people who smoke more than 20 cigarettes per day compared with people who never smoked. AMD is diagnosed primarily with clinical examination that includes a special lens that focuses light of the slit lamp through the pupil. Exudative neovascular AMD is best identified using angiography and by optical coherence tomography. Individuals with AMD who take nutritional supplements consisting of high-dose vitamin C, vitamin E, carotenoids, and zinc have a 20% probability to progress to late-stage AMD at 5 years vs a 28% probability for those taking a placebo. In exudative neovascular AMD, 94.6% of patients receiving monthly intravitreal anti-vascular endothelial growth factor (anti-VEGF) injections experience less than a 15-letter visual acuity loss after 12 months compared with 62.2% receiving sham treatment.
The prevalence of AMD is anticipated to increase worldwide to 288 million individuals by 2040. Intravitreally administered anti-VEGF treatment is first-line therapy for exudative neovascular AMD.
年龄相关性黄斑变性(AMD)影响了美国约 2000 万人和全球 1.96 亿人。AMD 是老年人严重视力损害的主要原因,预计到 2040 年,全球将有 2.88 亿人受到影响。
年龄较大、遗传因素和环境因素,如吸烟,与 AMD 的发展有关。当细胞外沉积物在视网膜外堆积时,就会发生 AMD,最终导致光感受器退化和中心视力丧失。AMD 的晚期特征是外视网膜萎缩,称为地图状萎缩,或与视网膜下和/或视网膜内渗出相关的新生血管形成,称为渗出性新生血管性 AMD。AMD 的年发病率范围为 55 至 59 岁人群中每 1000 人 0.3 例,90 岁或以上人群中每 1000 人 36.7 例。晚期 AMD 的估计遗传率约为 71%(95%CI,18%-88%)。长期前瞻性队列研究表明,与从不吸烟的人相比,每天吸烟超过 20 支的人 AMD 发病率明显更高。AMD 主要通过临床检查诊断,包括特殊镜片,该镜片通过瞳孔将光聚焦在裂隙灯上。渗出性新生血管性 AMD 最好通过血管造影和光学相干断层扫描来识别。服用高剂量维生素 C、维生素 E、类胡萝卜素和锌的营养补充剂的 AMD 患者,在 5 年内进展为晚期 AMD 的概率为 20%,而服用安慰剂的患者为 28%。在渗出性新生血管性 AMD 中,接受每月一次玻璃体内抗血管内皮生长因子(抗-VEGF)注射治疗的患者在 12 个月后视力丧失少于 15 个字母的比例为 94.6%,而接受假治疗的患者为 62.2%。
预计到 2040 年,全球 AMD 的患病率将增加到 2.88 亿人。玻璃体内给予的抗-VEGF 治疗是治疗渗出性新生血管性 AMD 的一线治疗方法。