Evidence mapPaperPMID 41311998Full record

ArticleThe EPMA journal2025

Multimodal AI-based modeling of glaucoma progression: a 3PM-guided approach integrating structural, functional, and vascular patterns.

Natalia I Kurysheva, Oxana Ye Rodionova, Alexey L Pomerantsev, Saina I Ponomareva, Olga Golubnitschaja

Abstract read
In one paragraph

Article in The EPMA journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Natalia I KuryshevaThe Ophthalmological Center of the Federal Medical and Biological Agency of the Russian Federation, 15 Gamalei Street, Moscow, 123098 Russian Federation.
Oxana Ye RodionovaFederal Research Center for Chemical Physics RAS, 4, Kosygin Street, Moscow, 119991 Russian Federation.
Alexey L PomerantsevFederal Research Center for Chemical Physics RAS, 4, Kosygin Street, Moscow, 119991 Russian Federation.
Saina I PonomarevaThe Ophthalmological Center of the Federal Medical and Biological Agency of the Russian Federation, 15 Gamalei Street, Moscow, 123098 Russian Federation.
Olga GolubnitschajaPredictive, Preventive and Personalised (3P) Medicine, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, 53127 Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glaucoma remains the leading cause of irreversible blindness worldwide. The development of predictive, preventive, and personalized medicine (3PM) strategies in the area is essential to address high inter-individual heterogeneity in glaucoma progression, in order to effectively protect stratified patients against disease progression. Aim: This study aims to develop and validate a personalized, multimodal predictive modeling framework that integrates structural, functional, and vascular biomarkers for individualized risk stratification of progression rates in primary open-angle glaucoma (POAG). Methods: Patients with POAG at varying stages were monitored for at least 36 months and underwent comprehensive multimodal evaluation, including structural optical coherence tomography (OCT), OCT angiography (OCT-A), automated perimetry, and biomechanical assessments. Predictive modeling was performed using Ranked Partial Least Squares Discriminant Analysis (Ranked PLS-DA). Model performance and variable importance were established through Procrustes Cross-Validation and optimization procedures. Results and data interpretation in the framework of 3PM: The final models included up to 27 parameters in early-stage POAG and 20 in advanced disease, leading to high prognostic accuracy (AUC up to 0.90) for classifying slow, moderate, and rapid rates of glaucoma progression. Feature importance analysis demonstrated that different biomarkers dominate at different disease stages: RNFL thickness, peripapillary microvascular dropout, parafoveal vascular density and corneal hysteresis in early POAG, while age, ganglion cell complex thickness, specific macular thickness measures, and peripapillary perfusion parameters were most predictive in advanced stages. Conclusions and 3PM-relevant outlook: The proposed innovation utilizes multimodal predictive disease modeling that supports accurate risk stratification, personalized glaucoma management and individualized protection against disease progression. Successful clinical application requires initial profiling, regular model recalibration, and adaptive treatment strategies - altogether leading to improved visual outcomes in stratified patients and leveraging resources used.

Indexed as

Application of AI in medicineBiomarker panelsDisease modelingGlaucoma progressionImproved individual outcomesIndividualized protection against irreversible blindnessMachine learningMulti-modal risk assessmentOCT-angiographyPatient phenotyping and stratificationPredictive preventive personalized medicine (PPPM / 3PM)Primary open-angle glaucoma

Identifiers

PMID41311998
PMCPMC12647416

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.