Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, Melbourne, Australia.
Ophthalmology, Department of Surgery, The University of Melbourne, Melbourne, Australia.
Clin Exp Ophthalmol. 2020 Sep;48(7):983-995. doi: 10.1111/ceo.13837. Epub 2020 Sep 2.
Multimodal imaging (MMI) allows a more granular grading of age-related macular degeneration (AMD) disease severity, with many novel risk factors having been recently identified. With this imaging information, we are better able to counsel our patients with more accurate and individualized progression scenarios. MMI also allows identification of anatomical features that increase our understanding of disease processes involved in progression to late AMD. Treatment protocols for neovascular AMD (nAMD) depend largely on the optical coherence tomography (OCT) appearance to determine disease activity, which allows us to individualize treatment. In geographic atrophy (GA), new intervention trials require the ability to define the extent of GA, so that GA growth rate can be determined. This is achieved through fundus autofluorescence (FAF) imaging, which allows greater accuracy of border identification, as well as revealing FAF patterns predictive of growth rates. As we strive to bring interventions earlier in the disease course, OCT imaging provides an ability to identify the first signs of atrophy, which may serve as novel surrogate biomarkers for GA, thereby facilitating trials. In the future, the use of artificial intelligence (AI) to automatically identify relevant features on MMI could further enhance our ability to determine disease severity, predict progression and assist in identifying disease activity parameters to support clinical decision making when treating nAMD. Newer developments may allow frequent, remote capturing of images, reducing clinic visits, detecting progression and monitoring neovascular activity in-between clinic visits. Being aware of these new imaging insights in AMD, greatly enhance our clinical management of AMD.
多模态成像(MMI)可以更精细地对年龄相关性黄斑变性(AMD)的严重程度进行分级,最近已经确定了许多新的危险因素。有了这些成像信息,我们就能更好地为患者提供更准确和个体化的进展预测。MMI 还可以识别增加我们对疾病进展过程的理解的解剖特征。新生血管性 AMD(nAMD)的治疗方案在很大程度上取决于光学相干断层扫描(OCT)的表现,以确定疾病的活动程度,从而使我们能够进行个体化治疗。在地图样萎缩(GA)中,新的干预试验需要确定 GA 的范围的能力,以便确定 GA 的增长率。这是通过眼底自发荧光(FAF)成像来实现的,该技术可以更准确地识别边界,并且可以揭示与增长率相关的 FAF 模式。随着我们努力在疾病早期进行干预,OCT 成像提供了识别萎缩最初迹象的能力,这可能成为 GA 的新替代生物标志物,从而促进临床试验。在未来,人工智能(AI)用于自动识别 MMI 上的相关特征,可以进一步增强我们确定疾病严重程度、预测进展和协助识别疾病活动参数的能力,以支持治疗 nAMD 时的临床决策。新的发展可能允许频繁、远程采集图像,减少就诊次数,在就诊之间检测进展和监测新生血管活动。了解 AMD 中的这些新的成像见解,可以极大地增强我们对 AMD 的临床管理。