Christian Doppler Laboratory for Ophthalmic Image Analysis, Vienna Reading Center, Department of Ophthalmology and Optometry, Medical University of Vienna, Vienna, Austria.
Christian Doppler Laboratory for Ophthalmic Image Analysis, Vienna Reading Center, Department of Ophthalmology and Optometry, Medical University of Vienna, Vienna, Austria.
Am J Ophthalmol. 2020 Aug;216:257-270. doi: 10.1016/j.ajo.2020.03.042. Epub 2020 Apr 8.
To quantitatively measure hyperreflective foci (HRF) during the progression of geographic atrophy (GA) secondary to age-related macular degeneration (AMD) using deep learning (DL) and investigate the association with local and global growth of GA.
Eyes with GA were prospectively included. Spectral-domain optical coherence tomography (SDOCT) and fundus autofluorescence images were acquired every 6 months. A 500-μm-wide junctional zone adjacent to the GA border was delineated and HRF were quantified using a validated DL algorithm. HRF concentrations in progressing and nonprogressing areas, as well as correlations between HRF quantifications and global and local GA progression, were assessed.
A total of 491 SDOCT volumes from 87 eyes of 54 patients were assessed with a median follow-up of 28 months. Two-thirds of HRF were localized within a millimeter adjacent to the GA border. HRF concentration was positively correlated with GA progression in unifocal and multifocal GA (all P < .001) and de novo GA development (P = .037). Local progression speed correlated positively with local increase of HRF (P value range <.001-.004). Global progression speed, however, did not correlate with HRF concentrations (P > .05). Changes in HRF over time did not have an impact on the growth in GA (P > .05).
Advanced artificial intelligence (AI) methods in high-resolution retinal imaging allows to identify, localize, and quantify biomarkers such as HRF. Increased HRF concentrations in the junctional zone and future macular atrophy may represent progressive migration and loss of retinal pigment epithelium. AI-based biomarker monitoring may pave the way into the era of individualized risk assessment and objective decision-making processes. NOTE: Publication of this article is sponsored by the American Ophthalmological Society.
利用深度学习(DL)定量测量与年龄相关性黄斑变性(AMD)相关的地图状萎缩(GA)进展过程中的高反射焦点(HRF),并探讨其与 GA 局部和整体增长的关系。
前瞻性纳入 GA 眼。每 6 个月采集一次光谱域光学相干断层扫描(SDOCT)和眼底自发荧光图像。在 GA 边界附近划定一个 500μm 宽的交界区,并使用经过验证的 DL 算法对 HRF 进行定量。评估进展区和非进展区的 HRF 浓度,以及 HRF 定量与 GA 局部和整体进展之间的相关性。
共评估了 54 例 87 只眼的 491 个 SDOCT 容积,中位随访时间为 28 个月。三分之二的 HRF 定位于 GA 边界附近一毫米内。在单灶和多灶 GA(均 P <.001)和新发病灶 GA 发展中,HRF 浓度与 GA 进展呈正相关(P <.001)。局部进展速度与 HRF 局部增加呈正相关(P 值范围<.001-.004)。然而,全局进展速度与 HRF 浓度无相关性(P >.05)。HRF 随时间的变化对 GA 增长没有影响(P >.05)。
高分辨率视网膜成像的先进人工智能(AI)方法可识别、定位和定量分析 HRF 等生物标志物。交界区 HRF 浓度增加和未来的黄斑萎缩可能代表视网膜色素上皮的进行性迁移和丢失。基于 AI 的生物标志物监测可能为个体化风险评估和客观决策过程开辟道路。