Evidence map›Paper›PMID 40961986›Full record

ArticleOphthalmology2026

The Association between Glaucoma and Dementia in a National Cohort of All of Us Participants.

Kenneth Pham, Rebecca Salowe, Isabel Di Rosa, Ali G Hamedani, Gui-Shuang Ying, Joan M O'Brien

Abstract readMulticenter Study
In one paragraph

Article in Ophthalmology, 2026. 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

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

2 citing papers in PubMed.

  1. Ocular Glymphatic System: Its Modulation and Role in Intraocular Tumors.Investigative ophthalmology & visual science · 2026
    Review
  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

6 authors.

Kenneth PhamPenn Medicine Center for Genetics of Complex Disease, Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Rebecca SalowePenn Medicine Center for Genetics of Complex Disease, Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Isabel Di RosaPenn Medicine Center for Genetics of Complex Disease, Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Ali G HamedaniDepartment of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Leonard Davis Institute for Health Economics, University of Pennsylvania, Philadelphia, Pennsylvania.
Gui-Shuang YingDepartment of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Center for Preventive Ophthalmology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Joan M O'BrienPenn Medicine Center for Genetics of Complex Disease, Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. Electronic address: joan.obrien@pennmedicine.upenn.edu.

Funding

Scientific TransparencyP30EY001583 · NEI · UNIVERSITY OF PENNSYLVANIA · PI CLAIRE H MITCHELL · 1985 to 2026
$19.5M
Primary Open Angle African-American Glaucoma Genetics Study RenewalR01EY023557 · NEI · UNIVERSITY OF PENNSYLVANIA · PI O'BRIEN, JOAN M · 2014 to 2025
$18.1M
NEI NIH HHS P30 EY001583NEI NIH HHS R01 EY023557
6 · The paper itself

Abstract

purposeTo assess the association between glaucoma and its subtypes and incidence of dementia and its subtypes across APOE genotypes in the National Institutes of Health (NIH) All of Us Research Program.

designRetrospective, longitudinal cohort study.

participantsA cohort of individuals with linked electronic health record (EHR) data in the All of Us dataset, with every individual with a glaucoma diagnosis matched with four control participants. Participants diagnosed with dementia before glaucoma were excluded.

methodsA 1:4 cohort of participants with glaucoma and control participants was created using a propensity score-matching design that considered age, race, ethnicity, and sex. Participants with whole-genome sequencing data were stratified by APOE genotype for sub-analyses. A multivariable Cox regression model was used to adjust for residual imbalance in comorbidities.

main outcome measuresIncidence of dementia and its subtypes.

resultsAmong the 393 497 All of Us participants with linked EHRs, we identified 9444 individuals (2.40%) with glaucoma diagnoses (excluding participants with diagnoses of dementia before glaucoma) and 37 776 matched controls without glaucoma. During the observation period (median, 6.5 years; interquartile range, 3.3-10.7 years), dementia was diagnosed in 1127 individuals (2.39%). Glaucoma was associated with a significantly increased risk of all-cause dementia (adjusted hazard ratio [aHR], 1.23; 95% confidence interval [CI], 1.08-1.40), Alzheimer's disease (aHR, 1.60; 95% CI, 1.26-2.02), and vascular dementia (aHR, 1.38; 95% CI, 1.04-1.83). Among glaucoma subtypes, primary open-angle glaucoma (POAG, N = 5756) and normal-tension glaucoma (NTG, N = 1106) were linked to an elevated risk of Alzheimer's disease (POAG: aHR, 1.48, 95% CI, 1.11-1.96; NTG: aHR, 1.87, 95% CI, 1.09-3.18), whereas angle-closure glaucoma (N = 3150) showed no significant association (aHR, 1.49; 95% CI, 0.91-2.27). Glaucoma was associated with an increased risk of all-cause dementia across the three APOE genotypes assessed, (ε2ε3 > ε3ε3 > ε3ε4).

conclusionsGlaucoma was associated with a higher risk of dementia across APOE genotypes, with varying associations among glaucoma and dementia subtypes. FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

Indexed as

DementiaGlaucomaAgedAged, 80 and overApolipoproteins EElectronic Health RecordsFemaleGenotypeGlaucoma, Open-AngleHumansIncidenceIntraocular PressureLongitudinal StudiesMaleMiddle AgedPropensity ScoreApolipoproteins EAlzheimer’s diseaseAPOEDementiaGlaucomaPrimary open-angle glaucoma

Identifiers

PMID40961986
PMCPMC12981904

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.