Evidence map›Paper›PMID 41533942›Full record

ArticleInvestigative ophthalmology & visual science2025

The Association of Polygenic Risk Score With Glaucoma and Its Related Traits: Results From Two German Population-Based Studies.

Anna M Welzel, Caroline Brandl, Janina M Herold, Julia V Stingl, Esther M Hoffmann, Anthony P Khawaja, Martina E Zimmermann, Thomas Winkler, Klaus J Stark, Irene Schmidtmann and 9 more

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2025. 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

19 authors.

Anna M WelzelDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Caroline BrandlDepartment of Ophthalmology, University Hospital Regensburg, Regensburg, Germany.
Janina M HeroldDepartment of Genetic Epidemiology, University Regensburg, Regensburg, Germany.
Julia V StinglDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Esther M HoffmannDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Anthony P KhawajaNIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.
Martina E ZimmermannDepartment of Genetic Epidemiology, University Regensburg, Regensburg, Germany.
Thomas WinklerDepartment of Genetic Epidemiology, University Regensburg, Regensburg, Germany.
Klaus J StarkDepartment of Genetic Epidemiology, University Regensburg, Regensburg, Germany.
Irene SchmidtmannInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Philipp S WildPreventive Cardiology and Preventive Medicine, Center for Cardiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Karl J LacknerInstitute of Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Philipp LurzDepartment of Cardiology, Universitätsmedizin Mainz, Mainz, Germany.
Manfred E BeutelDepartment of Psychosomatic Medicine and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Untere Zahlbacher, Mainz, Germany.
Oliver TüscherDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Untere Zahlbacher, Mainz, Germany.
Julia Weinmann-MenkeDepartment of Nephrology, I. Department of Medicine, University Medical Center Mainz, Johannes Gutenberg University, Mainz, Germany.
Norbert PfeifferDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Iris M HeidDepartment of Genetic Epidemiology, University Regensburg, Regensburg, Germany.
Alexander K SchusterDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Genome-wide association studies have revealed many loci linked to glaucoma. The aim of this study was to explore the associations between a glaucoma polygenic risk score (GPRS) with glaucoma prevalence, intraocular pressure (IOP), and peripapillary retinal nerve fibre layer thickness (pRNFL) on a population-based level. Methods: Participants of the Gutenberg Health Study (aged 40-80 years) and the AugUR Study (aged 70-95 years), two German population-based studies, were included. Of participants with genetic assessment 12,147 had glaucoma grading, 8938 data on IOP, and 7844 data on pRNFL. Spectral-domain optical coherence tomography was used to measure pRNFL thickness and noncontact tonometry for IOP measurements. Glaucoma was graded according to the classification of the International Society for Geographic and Epidemiological Ophthalmology. GPRS was calculated using 2453 locus lead variants. Linear regression was conducted to evaluate the association of GPRS with IOP and pRNFL thickness and Poisson regression analysis for the association of GPRS with glaucoma prevalence. Age groups were divided in quartiles: 40-51, ≥52-62, ≥63-72, and ≥73-95 years. Results: Increased GPRS was significantly associated with increased glaucoma prevalence (Prevalence ratio: 1.84, 95% confidence interval [CI], 1.60-2.11; P = 2 × 10-16) and higher IOP (B-estimate = 0.54 mm Hg per SD of GRPS; 95% CI, 0.48-0.59; P = 2 × 10-16). Higher GPRS was associated with thinner global pRNFL (B-estimate = -0.61 µm per SD of GPRS on global pRNFL; 95% CI, -0.86 to -0.36; P = 1.2 × 10-6) with increasing age. There was an association in temporal-inferior, temporal-superior, nasal-inferior, nasal-superior, and nasal pRNFL sector. Conclusions: Higher GPRS is associated with glaucoma prevalence, higher IOP and thinner pRNFL in two population-based studies in Germany. These associations were particularly seen in older participants.

Indexed as

GlaucomaIntraocular PressureAdultAgedAged, 80 and overFemaleGenetic Risk ScoreGenome-Wide Association StudyGermanyHumansMaleMiddle AgedNerve FibersPrevalenceRetinal Ganglion CellsRisk Factors

Identifiers

PMID41533942
PMCPMC12758419

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.