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medRxiv : the preprint server for health sciences · 2026

Genetic discovery using deep learning-derived optic nerve integrity phenotypes.

СтатьяПрепринтНазвание и аннотация: Перевод пока не подготовлен
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Aman Asma M, Zaher Eslam, Diaz-Torres Santiago, Driessen Sjoerd J, de Vries Victor A, van der Heide Frank Ct, Kolovos Antonia, Schmidt Joshua M, Marshall Henry N, Saleh Lania, Schulze Alicia, Blokland Gabriëlla A, Webers Carroll A, van der Kallen Carla J, Wesselius Anke, Arts Ilja, van Asten Freekje, Gorski Mathias, Zimmermann Martina E, Stark Klaus J, Heid Iris M, Young Terri L, Pasquale Louis R, Segrè Ayellet V, Wiggs Janey L, Khawaja Anthony P, Zack Donald J, Wong Raymond C, Hewitt Alex W, Schuster Alexander K, Berendschot Tos T, Thiadens Alberta A, van Garderen Karin A, Klaver Caroline C W, Hysi Pirro G, Hammond Christopher J, Brandl Caroline, Craig Jamie E, Ramdas Wishal D, Wang Ya Xing, Jonas Jost B, Roosta Fred, Hunter Michael L, MacGregor Stuart, Lee Samantha S, Mackey David A, Trzaskowski Maciej, Gharahkhani Puya

Аннотация

The peripapillary retinal nerve fibre layer (pRNFL) thickness and Bruch's membrane opening-minimum rim width (BMO-MRW) are three-dimensional retinal biomarkers for glaucoma. We aimed to demonstrate that AI-derived thickness from two-dimensional fundus images can act as proxies, enabling the discovery of novel neurodegenerative loci. AI-derived pRNFL and BMO-MRW strongly correlated with OCT-derived thickness (r: 0.69 and 0.79, respectively). After validation, these phenotypes were predicted in two cohorts lacking disc-centred OCT: the UK Biobank and the Canadian Longitudinal Study on Aging. The predicted phenotypes showed strong genetic correlations with directly measured phenotypes from a previous study for both phenotypes (0.70 and 0.96, respectively). This data increased statistical power, identifying 29 loci for pRNFL thickness and 122 loci for BMO-MRW, including 14 loci that were independent of VCDR. We observed shared and sector-specific thickness loci overlapping glaucoma loci and revealed loci independent of known risk factors. Together, these results emphasise that multidimensional inferences can be drawn from 2D imaging, enabling downstream genetic analyses.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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