Evidence map›Paper›PMID 42022047›Full record

ArticleOphthalmology science2026

Retinomics as a Tool for Glaucoma Prediction.

Mayinuer Yusufu, Selena Wei Zhang, Robert N Weinreb, Chen Zhou, Mengtian Kang, Xianwen Shang, Mingguang He, Danli Shi

Abstract read
In one paragraph

Article in Ophthalmology science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Mayinuer YusufuCentre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Selena Wei ZhangSchool of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.
Robert N WeinrebHamilton Glaucoma Center, Viterbi Family Department of Ophthalmology and the Shiley Eye Institute, University of California San Diego, La Jolla, California.
Chen ZhouBeijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Mengtian KangBeijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Xianwen ShangSchool of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.
Mingguang HeSchool of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.
Danli ShiSchool of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To investigate retinomic changes preceding glaucoma onset and explore their predictive value. Design: A population-based, prospective cohort study. Participants: 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. Methods: 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. Main Outcome Measures: Glaucoma status. Results: 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. Conclusions: 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. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

GlaucomaPredictionRetinal biomarkerRisk stratification

Identifiers

PMID42022047
PMCPMC13096955

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.