Evidence map›Paper›PMID 41057713›Full record

ArticleEye (London, England)2025

Risk factors associated with beta-peripapillary atrophy in individuals of African ancestry with primary open-angle glaucoma.

Tzuriel Sapir, Rebecca Salowe, Yineng Chen, Yan Zhu, Roy Lee, Ebenezer Daniel, Prithvi Sankar, Victoria Addis, Eydie Miller, Gui-Shuang Ying and 1 more

Abstract read
In one paragraph

Article in Eye (London, England), 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. 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

11 authors.

Tzuriel SapirCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-1689-2176
Rebecca SaloweCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Yineng ChenCenter for Preventive Ophthalmology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Yan ZhuCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Roy LeeCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Ebenezer DanielCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Prithvi SankarCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Victoria AddisCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Eydie MillerCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Gui-Shuang YingCenter for Preventive Ophthalmology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Joan M O'BrienCenter for Genetics of Complex Disease, Ophthalmology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. joan.obrien@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0003-4109-2928

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

backgroundBeta-Peripapillary Atrophy (beta-PPA) is an optic nerve head change associated with primary open-angle glaucoma (POAG). We evaluated demographic, ocular, and genetic risk factors for beta-PPA in individuals of African ancestry with POAG.

methodsPOAG cases were recruited from the Primary Open-Angle African American Glaucoma Genetics (POAAGG) study. Beta-PPA was defined as hypopigmentation with visible choroidal vessels and sclera adjacent to the optic disc. Univariable and multivariable regression models assessed risk factors for the presence and extent of beta-PPA.

resultsAmong 3381 eyes, 969 (28.6%) had beta-PPA. Beta-PPA was associated with older age (OR = 2.90, p < 0.001) and larger vertical cup-to-disc ratio (CDR) (OR = 1.58, p = 0.007), and was less common in females (OR = 0.53, p < 0.001). Beta-PPA presence was negatively associated with grey crescent (OR = 0.47, p = 0.01), neural rim notching (OR = 0.43, p = 0.01), and cylindrical (OR = 0.55, p < 0.001) or bean pot cup shapes (OR = 0.59, p < 0.001). Larger beta-PPA area was linked to older age (p = 0.008) and large vertical CDR (p = 0.03), but was less likely with conus pigmentosus (p = 0.001), deeper cup depth (p = 0.006), higher IOP (p = 0.005), and rounder discs (p = 0.01). Higher polygenic risk score (p = 0.007) and presence of the SNP rs34957764 in ROCK1P1 (p = 0.053) were associated with beta-PPA, but the same SNP was also associated with lesser area of beta-PPA (p = 0.03). Regions of beta-PPA correlated with greater RNFL loss (p < 0.01).

conclusionsBeta-PPA is strongly associated with older age and high CDR among individuals with POAG. These regions are vulnerable to RNFL loss.

Indexed as

Black or African AmericanGlaucoma, Open-AngleOptic AtrophyOptic DiskAdultAgedFemaleHumansIntraocular PressureMaleMiddle AgedNerve FibersRisk FactorsTomography, Optical CoherenceVisual Fields

Identifiers

PMID41057713
PMCPMC12623487

What OpenQuestion holds

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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.