Rapid measurement and machine learning classification of colour vision deficiency.
colour detection
colour discrimination
colour vision deficiency
cone-isolating directions
k-means clustering
unsupervised machine learning
vision diagnostics
Journal
Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists)
ISSN: 1475-1313
Titre abrégé: Ophthalmic Physiol Opt
Pays: England
ID NLM: 8208839
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
revised:
14
07
2023
received:
16
06
2023
accepted:
20
07
2023
pmc-release:
01
11
2024
medline:
23
10
2023
pubmed:
17
8
2023
entrez:
17
8
2023
Statut:
ppublish
Résumé
Colour vision deficiencies (CVDs) indicate potential genetic variations and can be important biomarkers of acquired impairment in many neuro-ophthalmic diseases. However, CVDs are typically measured with tests which possess high sensitivity for detecting the presence of a CVD but do not quantify its type or severity. In this study, we introduce Foraging Interactive D-prime (FInD), a novel computer-based, generalisable, rapid, self-administered vision assessment tool and apply it to colour vision testing. This signal detection theory-based adaptive paradigm computed test stimulus intensity from d-prime analysis. Stimuli were chromatic Gaussian blobs in dynamic luminance noise, and participants clicked on cells that contained chromatic blobs (detection) or blob pairs of differing colours (discrimination). Sensitivity and repeatability of FInD colour tasks were compared against the Hardy-Rand-Rittler and the Farnsworth-Munsell 100 hue tests in 19 colour-normal and 18 inherited colour-atypical, age-matched observers. Rayleigh colour match was also completed. Detection and discrimination thresholds were higher for atypical than for typical observers, with selective threshold elevations corresponding to unique CVD types. Classifications of CVD type and severity via unsupervised machine learning confirmed functional subtypes. FInD tasks reliably detect inherited CVDs, and may serve as valuable tools in basic and clinical colour vision science.
Identifiants
pubmed: 37589437
doi: 10.1111/opo.13210
pmc: PMC10592291
mid: NIHMS1920629
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1379-1390Subventions
Organisme : NEI NIH HHS
ID : R01 EY029713
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY032162
Pays : United States
Organisme : NIH HHS
ID : R01 EY029713
Pays : United States
Commentaires et corrections
Type : UpdateOf
Informations de copyright
© 2023 The Authors. Ophthalmic and Physiological Optics published by John Wiley & Sons Ltd on behalf of College of Optometrists.
Références
J Vis. 2021 Jul 6;21(7):15
pubmed: 34313713
Surv Ophthalmol. 2016 Mar-Apr;61(2):132-55
pubmed: 26656928
Stat Methods Med Res. 1999 Jun;8(2):135-60
pubmed: 10501650
Appl Opt. 1987 Apr 15;26(8):1441-8
pubmed: 20454340
Nat Commun. 2021 Apr 6;12(1):2078
pubmed: 33824310
Vision Res. 2011 Apr 13;51(7):633-51
pubmed: 21167193
Proc Biol Sci. 1994 Dec 22;258(1353):327-34
pubmed: 7886066
Vision Res. 1999 Aug;39(17):2901-27
pubmed: 10492818
Dev Med Child Neurol. 2023 Oct;65(10):1379-1386
pubmed: 37012700
Invest Ophthalmol Vis Sci. 1996 Dec;37(13):2771-4
pubmed: 8977494
Vision Res. 2000;40(13):1711-37
pubmed: 10814758
Behav Res Methods. 2022 Jun;54(3):1148-1160
pubmed: 34463952
Vis Neurosci. 2004 May-Jun;21(3):431-6
pubmed: 15518225
PLoS One. 2021 May 21;16(5):e0251903
pubmed: 34019572
Nat Neurosci. 1999 Oct;2(10):884-8
pubmed: 10491608
Clin Exp Optom. 2006 Mar;89(2):73-80
pubmed: 16494609
Fac Rev. 2020 Nov 13;9:8
pubmed: 33659940
Vis Neurosci. 2004 May-Jun;21(3):483-5
pubmed: 15518234
Optom Vis Sci. 1995 Aug;72(8):547-51
pubmed: 8539021