A foundation model for generalizable disease detection from retinal images

Yukun Zhou*, Mark A. Chia, Siegfried K. Wagner, Murat S. Ayhan, Dominic J. Williamson, Robbert R. Struyven, Timing Liu, Moucheng Xu, Mateo G. Lozano, Peter Woodward-Court, Yuka Kihara, Andre Altmann, Aaron Y. Lee, Eric J. Topol, Alastair K. Denniston, Daniel C. Alexander, Pearse A. Keane*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Medical artificial intelligence (AI) offers great potential for recognizing signs of health conditions in retinal images and expediting the diagnosis of eye diseases and systemic disorders1. However, the development of AI models requires substantial annotation and models are usually task-specific with limited generalizability to different clinical applications2. Here, we present RETFound, a foundation model for retinal images that learns generalizable representations from unlabelled retinal images and provides a basis for label-efficient model adaptation in several applications. Specifically, RETFound is trained on 1.6 million unlabelled retinal images by means of self-supervised learning and then adapted to disease detection tasks with explicit labels. We show that adapted RETFound consistently outperforms several comparison models in the diagnosis and prognosis of sight-threatening eye diseases, as well as incident prediction of complex systemic disorders such as heart failure and myocardial infarction with fewer labelled data. RETFound provides a generalizable solution to improve model performance and alleviate the annotation workload of experts to enable broad clinical AI applications from retinal imaging.
Original languageEnglish
Pages (from-to)156-163
Number of pages8
JournalNature
Volume622
Issue number7981
Early online date13 Sept 2023
DOIs
Publication statusPublished - 5 Oct 2023

Bibliographical note

Acknowledgements:
We thank P. Rawlinson for project management, C. Green and L. Wickham for information governance expertise, and A. Wenban, S. St John-Green and M. Barnfield for information technology support. This work is supported by Engineering and Physical Sciences Research Council grant nos. EP/M020533/1, EP/R014019/1 and EP/V034537/1, as well as the NIHR UCLH Biomedical Research Centre. S.K.W. is supported by a Medical Research Council Clinical Research Training Fellowship (grant no. MR/TR000953/1). P.A.K. is supported by a Moorfields Eye Charity Career Development Award (grant no. R190028A) and a UK Research & Innovation Future Leaders Fellowship (grant no. MR/T019050/1). For the purpose of open access, the author has applied a Creative Commons Attribution (CC BY) licence to any Author Accepted Manuscript version arising.

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