Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118715
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dc.contributorSchool of Optometryen_US
dc.contributorResearch Centre for SHARP Visionen_US
dc.creatorYusufu, Men_US
dc.creatorZhang, SWen_US
dc.creatorWeinreb, RNen_US
dc.creatorZhou, Cen_US
dc.creatorKang, Men_US
dc.creatorShang, Xen_US
dc.creatorHe, Men_US
dc.creatorShi, Den_US
dc.date.accessioned2026-05-13T06:19:56Z-
dc.date.available2026-05-13T06:19:56Z-
dc.identifier.urihttp://hdl.handle.net/10397/118715-
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.rights© 2026 American Academy of Ophthalmology, Incen_US
dc.rightsPublished by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Yusufu, M., Zhang, S. W., Weinreb, R. N., Zhou, C., Kang, M., Shang, X., He, M., & Shi, D. (2026). Retinomics as a Tool for Glaucoma Prediction. Ophthalmology Science, 6(5), 101163 is available at https://doi.org/10.1016/j.xops.2026.101163.en_US
dc.titleRetinomics as a tool for glaucoma predictionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume6en_US
dc.identifier.issue5en_US
dc.identifier.doi10.1016/j.xops.2026.101163en_US
dcterms.abstractPurpose: To investigate retinomic changes preceding glaucoma onset and explore their predictive value.en_US
dcterms.abstractDesign: A population-based, prospective cohort study.en_US
dcterms.abstractParticipants: A total of 40 949 adults from the UK Biobank, all with eligible color fundus photography (CFP) data and OCT data and without baseline glaucoma, were included in this study.en_US
dcterms.abstractMethods: We used baseline values of retinomics, a composite set of quantitative retinal imaging biomarkers including 135 retinal vascular measurements extracted with the Retina-based Microvascular Health Assessment System from CFP and 21 OCT-derived retinal layer measurements. After least absolute shrinkage and selection operator feature selection, Cox regression was used to assess associations with incident glaucoma, and a gradient boosting machine model was applied to evaluate predictive performance.en_US
dcterms.abstractMain Outcome Measures: Glaucoma status.en_US
dcterms.abstractResults: During a median follow-up of 12.49 years, 653 of 40 949 participants developed glaucoma. After adjusting for age, sex, ethnicity, education, smoking behavior, alcohol consumption, physical activity, hypertension, obesity, glycated hemoglobin, and intraocular pressure, 18 of the 48 least absolute shrinkage and selection operator-identified retinal parameters showed statistically significant associations with incident glaucoma, with each standard deviation change associated with 8.2% to 26.4% increased risk. These findings highlighted novel predictors beyond conventional parameters, including vascular network simplification and inner nuclear layer-related thickening. For a 12.49-year incident glaucoma prediction, simply using age, sex, and retinomic features, we achieved a concordance index of 0.767. After being stratified into 3 risk groups, the highest risk group showed a hazard ratio of 8.72 (95% confidence interval: 6.59–11.54) against the lowest risk group.en_US
dcterms.abstractConclusions: Our study revealed retinal vascular and neural alterations associated with increased risk of incident glaucoma. In addition, our study showed that retinomics can serve as an effective biomarker for identifying individuals at high risk of developing glaucoma. The simplicity (age, sex, and basic imaging) of our model along with its satisfactory risk stratification performance for long-term incident glaucoma suggest that it can be used to distinguish those patients who are most suitable for early therapeutic intervention to prevent blindness or severe visual impairment at a population level.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOphthalmology science, May 2026, v. 6, no. 5, 101163en_US
dcterms.isPartOfOphthalmology scienceen_US
dcterms.issued2026-05-
dc.identifier.eissn2666-9145en_US
dc.identifier.artn101163en_US
dc.description.validate202605 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera4416-
dc.identifier.SubFormID52747-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by the Start-up Fund for RAPs under the Strategic Hiring Scheme (P0048623) from HKSAR and PolyU-Stanford Joint Research Centre for Longitudinal Deep Omics (LDO) (P0056331). M.Y. is supported by the Melbourne Research Scholarship and Riady Scholarship established by the University of Melbourne. The funding source had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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