Evidence map›Paper›PMID 38734746›Full record

ArticleEye (London, England)2024

Ocular biomarkers: useful incidental findings by deep learning algorithms in fundus photographs.

Eve Martin, Angus G Cook, Shaun M Frost, Angus W Turner, Fred K Chen, Ian L McAllister, Janis M Nolde, Markus P Schlaich

Abstract read
In one paragraph

Article in Eye (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Eve MartinCommonwealth Scientific and Industrial Research Organisation (CSIRO), Kensington, WA, Australia. eve.martin@uwa.edu.au.ORCID http://orcid.org/0009-0000-0968-0100
Angus G CookSchool of Population and Global Health, The University of Western Australia, Crawley, Australia.
Shaun M FrostCommonwealth Scientific and Industrial Research Organisation (CSIRO), Kensington, WA, Australia.
Angus W TurnerLions Eye Institute, Nedlands, WA, Australia.ORCID http://orcid.org/0000-0001-5949-7451
Fred K ChenLions Eye Institute, Nedlands, WA, Australia.ORCID http://orcid.org/0000-0003-2809-9930
Ian L McAllisterLions Eye Institute, Nedlands, WA, Australia.
Janis M NoldeDobney Hypertension Centre - Royal Perth Hospital Unit, Medical School, The University of Western Australia, Perth, Australia.
Markus P SchlaichDobney Hypertension Centre - Royal Perth Hospital Unit, Medical School, The University of Western Australia, Perth, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesArtificial intelligence can assist with ocular image analysis for screening and diagnosis, but it is not yet capable of autonomous full-spectrum screening. Hypothetically, false-positive results may have unrealized screening potential arising from signals persisting despite training and/or ambiguous signals such as from biomarker overlap or high comorbidity. The study aimed to explore the potential to detect clinically useful incidental ocular biomarkers by screening fundus photographs of hypertensive adults using diabetic deep learning algorithms. SUBJECTS/

methodsPatients referred for treatment-resistant hypertension were imaged at a hospital unit in Perth, Australia, between 2016 and 2022. The same 45° colour fundus photograph selected for each of the 433 participants imaged was processed by three deep learning algorithms. Two expert retinal specialists graded all false-positive results for diabetic retinopathy in non-diabetic participants.

resultsOf the 29 non-diabetic participants misclassified as positive for diabetic retinopathy, 28 (97%) had clinically useful retinal biomarkers. The models designed to screen for fewer diseases captured more incidental disease. All three algorithms showed a positive correlation between severity of hypertensive retinopathy and misclassified diabetic retinopathy.

conclusionsThe results suggest that diabetic deep learning models may be responsive to hypertensive and other clinically useful retinal biomarkers within an at-risk, hypertensive cohort. Observing that models trained for fewer diseases captured more incidental pathology increases confidence in signalling hypotheses aligned with using self-supervised learning to develop autonomous comprehensive screening. Meanwhile, non-referable and false-positive outputs of other deep learning screening models could be explored for immediate clinical use in other populations.

Indexed as

AlgorithmsBiomarkersDeep LearningDiabetic RetinopathyIncidental FindingsAdultAgedFemaleFundus OculiHumansHypertensionMaleMiddle AgedPhotographyBiomarkers

Identifiers

PMID38734746
PMCPMC11385472

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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.