Evidence map›Paper›PMID 35113505›Full record

ArticleActa ophthalmologica2022

Limitation of standard pseudoisochromatic plates in identifying colour vision deficiencies when compared with genetic testing.

Solveig Arnegard, Rigmor C Baraas, Jay Neitz, Lene A Hagen, Maureen Neitz

Open access · hybridAbstract read
In one paragraph

Article in Acta ophthalmologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. iPhone-based anomaloscope for accessible, accurate color vision testing.Journal of the Optical Society of America. A, Optics, image science, and vision · 2025
    Article
  2. Article
  3. 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

5 authors at 2 institutions in 2 countries.

Solveig ArnegardNational Centre for Optics, Vision and Eye Care, Faculty of Health and Social Sciences, University of South-Eastern Norway, Kongsberg, Norway.ORCID https://orcid.org/0000-0003-1394-453X
Rigmor C BaraasNational Centre for Optics, Vision and Eye Care, Faculty of Health and Social Sciences, University of South-Eastern Norway, Kongsberg, Norway.ORCID https://orcid.org/0000-0003-3259-7617
Jay NeitzDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.
Lene A HagenNational Centre for Optics, Vision and Eye Care, Faculty of Health and Social Sciences, University of South-Eastern Norway, Kongsberg, Norway.ORCID https://orcid.org/0000-0002-9017-4519
Maureen NeitzDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.
University of South-Eastern Norway · NOUniversity of Washington · US

Funding

Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI MAUREEN E NEITZ · 1985 to 2026
$23.5M
Role of a dual splicing and amino acid code in myopia, cone dysfunction and cone dystrophy associated with L/M opsin interchange mutationsR01EY028118 · NEI · UNIVERSITY OF WASHINGTON · PI NEITZ, MAUREEN E · 2018 to 2022
$2.2M
National Institutes of Health/National Eye Institute Grant NIH P30EY001730 and R01EY028118NEI NIH HHS P30 EY001730NEI NIH HHS R01 EY028118Research to Prevent BlindnessThe Oslofjord Fund Norway Grant 249049
6 · The paper itself

Abstract

purposeThe Ishihara pseudoisochromatic (PIC) plate test is the most used test for identifying red-green colour-deficient individuals, but it is not known how the Ishihara results compare with that of genetics testing. Here, the outcome of genotype analysis of OPN1LW and OPN1MW was compared with that of the Ishihara (24-plate ed., 1964) and the Hardy-Rand-Rittler (4th ed. 2002) PIC plate tests.

methodsHealthy participants with normal habitual visual acuity (n = 454, 16-24 years; 193 males; logMAR ≤ 0.00) gave saliva samples for opsin gene analysis and performed the two PIC plate tests as part of a cross-sectional study. The criteria for failing the PIC tests were according to manufacturers' instructions. DNA was extracted and used in genotyping assays of OPN1LW and OPN1MW genes from each participant using the Agena MassArray genotyping system.

resultsTen male (5.2%) and 3 (1.1%) female participants were identified as red-green colour deficient based on PIC tests alone. The combination of MassArray and PIC test results identified 10.4% of male and 0.8% of female participants to be colour deficient (males: 0.5% protan and 9.9% deutan; females: 0.8% deutan). Hardy-Weinberg calculations based on male frequencies from combining the MassArray and the PIC test results gave female frequency estimates of colour deficiency and carriers closely matching measured frequencies.

conclusionsMassArray identified twice as many colour-deficient males as identified from PIC tests alone. Combining results from MassArray and the PIC tests proves to be more reliable than any single test at correctly identifying red-green colour-deficient individuals and carriers.

Indexed as

Color Vision DefectsColor Perception TestsCross-Sectional StudiesDNAFemaleGenetic TestingHumansMaleOpsinsDNAOpsinscolour vision deficiencycolour vision testinggenetic testingHardy-Rand-Rittler testIshihara testopsin genes

Identifiers

PMID35113505
PMCPMC9614865
OpenAlexW4210381783

What OpenQuestion holds

Textmetadata
LicenceTDM
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.