Evidence map›Paper›PMID 38703802›Full record

ArticleAmerican journal of ophthalmology2024

Progression or Aging? A Deep Learning Approach for Distinguishing Glaucoma Progression From Age-Related Changes in OCT Scans.

Sayan Mandal, Alessandro A Jammal, Davina Malek, Felipe A Medeiros

Abstract read
In one paragraph

Article in American journal of ophthalmology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Artificial Intelligence in Glaucoma Detection and Progression.Advances in ophthalmology and optometry · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Big data for imaging assessment in glaucoma.Taiwan journal of ophthalmology
    Review
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

4 authors.

Sayan MandalFrom the Department of Electrical and Computer Engineering, Pratt School of Engineering (S.M., F.A.M.), Duke University, Durham, North Carolina, USA.
Alessandro A JammalDuke Eye Center and Department of Ophthalmology (A.A.J., F.A.M.), Duke University, Durham, North Carolina, USA; Bascom Palmer Eye Institute (A.A.J., D.M., F.A.M.), University of Miami, Miami, Florida, USA.
Davina MalekBascom Palmer Eye Institute (A.A.J., D.M., F.A.M.), University of Miami, Miami, Florida, USA.
Felipe A MedeirosFrom the Department of Electrical and Computer Engineering, Pratt School of Engineering (S.M., F.A.M.), Duke University, Durham, North Carolina, USA; Duke Eye Center and Department of Ophthalmology (A.A.J., F.A.M.), Duke University, Durham, North Carolina, USA; Bascom Palmer Eye Institute (A.A.J., D.M., F.A.M.), University of Miami, Miami, Florida, USA. Electronic address: fmedeiros@med.miami.edu.

Funding

Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Dmitry V Ivanov · 2004 to 2026
$12.2M
The BCI (Brain Computer Interface) Glaucoma Study: Objective Home-Based Detection of Progressive Visual Function Loss in GlaucomaR01EY029885 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ASRANI, SANJAY, MEDEIROS, FELIPE · 2019 to 2022
$2.2M
Objective Quantification of Neural Damage for Screening, Diagnosis and Monitoring of Glaucoma with Fundus PhotographsR21EY031898 · NEI · DUKE UNIVERSITY · PI MEDEIROS, FELIPE · 2020 to 2021
$437k
NEI NIH HHS P30 EY014801NEI NIH HHS R01 EY029885NEI NIH HHS R21 EY031898
6 · The paper itself

Abstract

purposeTo develop deep learning (DL) algorithm to detect glaucoma progression using optical coherence tomography (OCT) images, in the absence of a reference standard.

designRetrospective cohort study.

methodsGlaucomatous and healthy eyes with ≥5 reliable peripapillary OCT (Spectralis, Heidelberg Engineering) circle scans were included. A weakly supervised time-series learning model, called noise positive-unlabeled (Noise-PU) DL was developed to classify whether sequences of OCT B-scans showed glaucoma progression. The model used 2 learning schemes, one to identify age-related changes by differentiating test sequences from glaucoma vs healthy eyes, and the other to identify test-retest variability based on scrambled OCTs of glaucoma eyes. Both models' bases were convolutional neural networks (CNN) and long short-term memory (LSTM) networks which were combined to form a CNN-LSTM model. Model features were combined and jointly trained to identify glaucoma progression, accounting for age-related loss. The DL model's outcomes were compared with ordinary least squares (OLS) regression of retinal nerve fiber layer (RNFL) thickness over time, matched for specificity. The hit ratio was used as a proxy for sensitivity.

resultsEight thousand seven hundred eighty-five follow-up sequences of 5 consecutive OCT tests from 3253 eyes (1859 subjects) were included in the study. The mean follow-up time was 3.5 ± 1.6 years. In the test sample, the hit ratios of the DL and OLS methods were 0.498 (95%CI: 0.470-0.526) and 0.284 (95%CI: 0.258-0.309) respectively (P < .001) when the specificities were equalized to 95%.

conclusionA DL model was able to identify longitudinal glaucomatous structural changes in OCT B-scans using a surrogate reference standard for progression.

Indexed as

AgingDeep LearningDisease ProgressionIntraocular PressureNerve FibersOptic DiskRetinal Ganglion CellsTomography, Optical CoherenceVisual FieldsAgedAlgorithmsFemaleFollow-Up StudiesGlaucomaGlaucoma, Open-AngleHumans

Identifiers

PMID38703802
PMCPMC12307053

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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.