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Structural and Functional Characteristics of Color Vision Changes in Choroideremia.
Jolly, Jasleen K; Simunovic, Matthew P; Dubis, Adam M; Josan, Amandeep S; Robson, Anthony G; Bellini, Marco P; Bloch, Edward; Georgiadis, Odysseas; da Cruz, Lyndon; Bridge, Holly; MacLaren, Robert E.
Afiliación
  • Jolly JK; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
  • Simunovic MP; Oxford Eye Hospital and NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Dubis AM; Oxford Centre for Functional MRI of the Brain (FMRIB), Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford, United Kingdom.
  • Josan AS; Save Sight Institute, Discipline of Ophthalmology, University of Sydney, Sydney, NSW, Australia.
  • Robson AG; Retinal Unit Sydney Eye Hospital, Sydney, NSW, Australia.
  • Bellini MP; NIHR Biomedical Resource Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, United Kingdom.
  • Bloch E; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
  • Georgiadis O; Oxford Eye Hospital and NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • da Cruz L; Electrophysiology Department, Moorfields Eye Hospital, London, United Kingdom.
  • Bridge H; University College London Institute of Ophthalmology, London, United Kingdom.
  • MacLaren RE; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Front Neurosci ; 15: 729807, 2021.
Article en En | MEDLINE | ID: mdl-34690675
ABSTRACT
Color vision is considered a marker of cone function and its assessment in patients with retinal pathology is complementary to the assessments of spatial vision [best-corrected visual acuity (BCVA)] and contrast detection (perimetry). Rod-cone and chorioretinal dystrophies-such as choroideremia-typically cause alterations to color vision, making its assessment a potential outcome measure in clinical trials. However, clinical evaluation of color vision may be compromised by pathological changes to spatial vision and the visual field. The low vision Cambridge Color Test (lvCCT) was developed specifically to address these latter issues. We used the trivector version of the lvCCT to quantify color discrimination in a cohort of 53 patients with choroideremia. This test enables rapid and precise characterization of color discrimination along protan, deutan, and tritan axes more reliably than the historically preferred test for clinical trials, namely the Farnsworth Munsell 100 Hue test. The lvCCT demonstrates that color vision defects-particularly along the tritan axis-are seen early in choroideremia, and that this occurs independent of changes in visual acuity, pattern electroretinography and ellipsoid zone area on optical coherence tomography (OCT). We argue that the selective loss of tritan color discrimination can be explained by our current understanding of the machinery of color vision and the pathophysiology of choroideremia.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido
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