Evidence map›Paper›PMID 42221027›Full record

ArticleFrontiers in aging neuroscience2026

Optical coherence tomography artefact burden predicts cognitive decline and incident dementia.

Serene Jia Ning Loke, Reuben Jyong Kiat Foo, Nur Fidyana Binte Abdul Gani, Damon Wong, Bingyao Tan, An Qi Toh, Narayanaswamy Venketasubramanian, Boon Yeow Tan, Christopher Li-Hsian Chen, Leopold Schmetterer and 1 more

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 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
0cells of the map it votes in
0citing 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

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

11 authors.

Serene Jia Ning Loke *Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Reuben Jyong Kiat Foo *Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Nur Fidyana Binte Abdul GaniSingapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Damon WongSingapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Bingyao TanSingapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
An Qi TohDepartments of Pharmacology and Psychological Medicine, Memory Aging and Cognition Centre, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Narayanaswamy VenketasubramanianDepartments of Pharmacology and Psychological Medicine, Memory Aging and Cognition Centre, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Boon Yeow TanSt Luke's Hospital, Singapore, Singapore.
Christopher Li-Hsian ChenDepartments of Pharmacology and Psychological Medicine, Memory Aging and Cognition Centre, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Leopold SchmettererSingapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Jacqueline ChuaSingapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Scalable, low-burden biomarkers for predicting cognitive decline remain needed. We hypothesised that OCT acquisition irregularities (commonly termed scan artefacts), which may reflect visuomotor and attentional instability during imaging, carry prognostic information for cognitive outcomes. Methods: We studied 507 Asian memory clinic participants who underwent baseline OCT imaging and comprehensive neuropsychological assessment annually for up to 5 years. OCT artefacts (motion, shadow, off-centre, refractive shift, out-of-boundary, and tilt) and signal strength were graded at baseline. Clinically significant cognitive decline was defined as a ≥ 0.5 standard deviation decrease in global cognitive z-score from baseline at any follow-up visit. Cox proportional hazards models evaluated associations between artefact burden and incident cognitive decline, adjusting for demographics, education, diabetes, and baseline cognitive status/diagnosis. Among participants with cognitive impairment no dementia (CIND) at baseline ( Results: Cognitive decline occurred in 289 participants (57%). Presence of any artefact was associated with higher risk of decline (HR = 1.37, 95% CI = 1.12-1.68, Conclusion: Routine OCT acquisition irregularities may provide an opportunistic, low-burden prognostic signal for cognitive vulnerability and dementia progression, complementing established neurodegenerative biomarkers.

Indexed as

Alzheimer’s diseasecognitive declinecognitive impairmentdementiaimaging artefactsneurodegenerationoptical coherence tomography (OCT)scan quality

Identifiers

PMID42221027
PMCPMC13219028

What OpenQuestion 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 OpenQuestion graph.