Multimodal, multitask, multiattention (M3) deep learning detection of reticular pseudodrusen: Toward automated and accessible classification of age-related macular degeneration

Author:

Chen Qingyu1ORCID,Keenan Tiarnan D.L2,Allot Alexis1,Peng Yifan1ORCID,Agrón Elvira2,Domalpally Amitha3,Klaver Caroline C. W4,Luttikhuizen Daniel T4,Colyer Marcus H5,Cukras Catherine A2,Wiley Henry E2,Teresa Magone M2,Cousineau-Krieger Chantal2,Wong Wai T26,Zhu Yingying78,Chew Emily Y2,Lu Zhiyong1,

Affiliation:

1. National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA

2. Division of Epidemiology and Clinical Applications, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA

3. Fundus Photograph Reading Center, University of Wisconsin, Madison, Wisconsin, USA

4. Department of Ophthalmology, Erasmus Medical Center, Rotterdam, the Netherlands

5. Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA

6. Section on Neuron-Glia Interactions in Retinal Disease, Laboratory of Retinal Cell and Molecular Biology, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA

7. Department of Computer Science and Engineering, University of Texas at Arlington, Arlington, Texas, USA

8. Department of Radiology, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA

Abstract

Abstract Objective Reticular pseudodrusen (RPD), a key feature of age-related macular degeneration (AMD), are poorly detected by human experts on standard color fundus photography (CFP) and typically require advanced imaging modalities such as fundus autofluorescence (FAF). The objective was to develop and evaluate the performance of a novel multimodal, multitask, multiattention (M3) deep learning framework on RPD detection. Materials and Methods A deep learning framework (M3) was developed to detect RPD presence accurately using CFP alone, FAF alone, or both, employing >8000 CFP-FAF image pairs obtained prospectively (Age-Related Eye Disease Study 2). The M3 framework includes multimodal (detection from single or multiple image modalities), multitask (training different tasks simultaneously to improve generalizability), and multiattention (improving ensembled feature representation) operation. Performance on RPD detection was compared with state-of-the-art deep learning models and 13 ophthalmologists; performance on detection of 2 other AMD features (geographic atrophy and pigmentary abnormalities) was also evaluated. Results For RPD detection, M3 achieved an area under the receiver-operating characteristic curve (AUROC) of 0.832, 0.931, and 0.933 for CFP alone, FAF alone, and both, respectively. M3 performance on CFP was very substantially superior to human retinal specialists (median F1 score = 0.644 vs 0.350). External validation (the Rotterdam Study) demonstrated high accuracy on CFP alone (AUROC, 0.965). The M3 framework also accurately detected geographic atrophy and pigmentary abnormalities (AUROC, 0.909 and 0.912, respectively), demonstrating its generalizability. Conclusions This study demonstrates the successful development, robust evaluation, and external validation of a novel deep learning framework that enables accessible, accurate, and automated AMD diagnosis and prognosis.

Publisher

Oxford University Press (OUP)

Subject

Health Informatics

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