Evidence map›Paper›PMID 29450497›Full record

Observational studyJAMA ophthalmology2018

Detection of Glaucoma Progression in Individuals of African Descent Compared With Those of European Descent.

Carolina P B Gracitelli, Linda M Zangwill, Alberto Diniz-Filho, Ricardo Y Abe, Christopher A Girkin, Robert N Weinreb, Jeffrey M Liebmann, Felipe A Medeiros

Open access · bronzeAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JAMA ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.3field-weighted citation impact, top 6% of its field
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

40 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  4. Evaluating a virtual reality visual fields analyzer in an urban, underserved glaucoma & glaucoma suspect patient populations to identify disparities.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
    Article
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  14. Review
  15. Observational
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  20. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Carolina P B GracitelliShiley Eye Institute, Department of Ophthalmology, University of California, San Diego, La Jolla.
Linda M ZangwillShiley Eye Institute, Department of Ophthalmology, University of California, San Diego, La Jolla.
Alberto Diniz-FilhoShiley Eye Institute, Department of Ophthalmology, University of California, San Diego, La Jolla.
Ricardo Y AbeShiley Eye Institute, Department of Ophthalmology, University of California, San Diego, La Jolla.
Christopher A GirkinSchool of Medicine, University of Alabama, Birmingham.
Robert N WeinrebShiley Eye Institute, Department of Ophthalmology, University of California, San Diego, La Jolla.
Jeffrey M LiebmannEdward S. Harkness Eye Institute, Columbia University Medical Center, New York, New York.
Felipe A MedeirosShiley Eye Institute, Department of Ophthalmology, University of California, San Diego, La Jolla.
University of California, San Diego · USColumbia University Irving Medical Center · USDuke University · USUniversity of Alabama at Birmingham · US

Funding

Vision BiostatisticsP30EY022589 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LINDA M ZANGWILL · 2012 to 2026
$10.3M
NEI NIH HHS P30 EY022589
6 · The paper itself

Abstract

Importance: Individuals of African descent have been reported to be at higher risk for becoming visually impaired from glaucoma compared with individuals of European descent. Objective: To investigate racial differences in longitudinal visual field variability and their impact on time to detect visual field progression. Design, Setting, and Participants: This multicenter prospective observational cohort study included 236 eyes of 173 individuals of European descent and 235 eyes of 171 individuals of African descent followed up for a mean (SD) time of 7.5 (3.4) years. Main Outcomes and Measures: Differences in test-retest variability and simulated time to detect progression in individuals of African descent and of European descent with glaucoma. Standard automated perimetry mean deviation values were regressed over time for each eye, and SD of the residuals was used as a measure of variability. Distributions of residuals were used in computer simulations to reconstruct "real-world" standard automated perimetry mean deviation trajectories under different assumptions about rate of change and frequency of testing. Times to detect progression were obtained for the simulated visual fields. Results: Among the 344 patients, the mean (SD) age at baseline was 60.2 (10.0) and 60.6 (9.0) years for individuals of African descent and of European descent, respectively; 94 (52%) and 86 (48%) of individuals of African descent and of European descent were women, respectively. The mean SD of the residuals was larger in eyes of individuals of African descent vs those of European descent (1.45 [0.83] dB vs 1.12 [0.48] dB; mean difference: 0.33 dB; 95% CI of the difference, 0.21-0.46; P < .001). The eyes in individuals of African descent had a larger increase in variability with worsening disease (P < .001). When simulations were performed assuming common progression scenarios, there was a delay to detect progression in eyes of individuals of African descent compared with those of European descent. For a scenario with baseline mean deviation of -10 dB and rate of change of -0.5 dB/y, detection of progression in individuals of African descent was delayed by 3.1 (95% CI, 2.9-3.2) years, when considered 80% power and annual tests. Conclusions and Relevance: Patients of African descent with glaucoma showed increased visual field variability compared with those of European descent, resulting in delayed detection of progression that may contribute to explain higher rates of glaucoma-related visual impairment in individuals of African descent compared with those of European descent with glaucoma.

Indexed as

Black or African AmericanVisual AcuityWhite PeopleDisease ProgressionFemaleFollow-Up StudiesGlaucomaHumansIntraocular PressureMaleMiddle AgedMorbidityProspective StudiesTime FactorsUnited StatesVisual Fields

Identifiers

PMID29450497
PMCPMC5876834
OpenAlexW2791412124

What OpenQuestion holds

Textmetadata
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.