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Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy

PURPOSE: The purpose of this study was to compare L-, M-, S-cone-, and rod-driven temporal contrast sensitivities (tCS) in patients with RP1L1-associated autosomal-dominant occult macular dystrophy (OMD), and to investigate how photoreceptor degeneration determines which post-receptoral channels dom...

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Autores principales: Huchzermeyer, Cord, Fars, Julien, Kremers, Jan, Kühlewein, Laura, Kempf, Melanie, Ott, Saskia, Stingl, Krunoslav, Stingl, Katarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289274/
https://www.ncbi.nlm.nih.gov/pubmed/37342031
http://dx.doi.org/10.1167/iovs.64.7.33
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author Huchzermeyer, Cord
Fars, Julien
Kremers, Jan
Kühlewein, Laura
Kempf, Melanie
Ott, Saskia
Stingl, Krunoslav
Stingl, Katarina
author_facet Huchzermeyer, Cord
Fars, Julien
Kremers, Jan
Kühlewein, Laura
Kempf, Melanie
Ott, Saskia
Stingl, Krunoslav
Stingl, Katarina
author_sort Huchzermeyer, Cord
collection PubMed
description PURPOSE: The purpose of this study was to compare L-, M-, S-cone-, and rod-driven temporal contrast sensitivities (tCS) in patients with RP1L1-associated autosomal-dominant occult macular dystrophy (OMD), and to investigate how photoreceptor degeneration determines which post-receptoral channels dominate perception. METHODS: Photoreceptor isolating stimuli were created with the silent substitution technique. Photoreceptor-selective tCS deviations (D (L-cone/M-cone/S-cone/Rod)) were obtained as a function of temporal frequency with identical retinal adaptation, by subtracting tCS from age-corrected normal values. A linear-mixed effects model was used for analysis. RESULTS: Eleven genetically confirmed patients were included (7 women, 5 men; age = 52.27 ± 14.44 years). Overall, L- and M-cone-driven sensitivity deviations (D(L-cone) and D(M-cone)) were more negative than D(S-cone); D(Rod) was normal at frequencies between 8 and 12 Hz in all subjects. Rod-driven tCS functions allowed identification of two subgroups of patients: one with band-pass properties and one with low-pass properties, suggesting dominance of different post-receptoral filters. The same filtering properties were observed in L-cone-driven tCS functions. Furthermore, the two subgroups also differed in clinical parameters (spherical equivalent, BCVA, perimetry, and ocular coherence tomography (OCT) reflectivity of the ellipsoid zone relative to the RPE). CONCLUSIONS: OMD was characterized predominantly by deterioration of L- and M-cone-cone driven function in the perifovea. Rod-driven functions were normal. Differences in the photoreceptor signals were further modified by postreceptoral filters.
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spelling pubmed-102892742023-06-24 Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy Huchzermeyer, Cord Fars, Julien Kremers, Jan Kühlewein, Laura Kempf, Melanie Ott, Saskia Stingl, Krunoslav Stingl, Katarina Invest Ophthalmol Vis Sci Retina PURPOSE: The purpose of this study was to compare L-, M-, S-cone-, and rod-driven temporal contrast sensitivities (tCS) in patients with RP1L1-associated autosomal-dominant occult macular dystrophy (OMD), and to investigate how photoreceptor degeneration determines which post-receptoral channels dominate perception. METHODS: Photoreceptor isolating stimuli were created with the silent substitution technique. Photoreceptor-selective tCS deviations (D (L-cone/M-cone/S-cone/Rod)) were obtained as a function of temporal frequency with identical retinal adaptation, by subtracting tCS from age-corrected normal values. A linear-mixed effects model was used for analysis. RESULTS: Eleven genetically confirmed patients were included (7 women, 5 men; age = 52.27 ± 14.44 years). Overall, L- and M-cone-driven sensitivity deviations (D(L-cone) and D(M-cone)) were more negative than D(S-cone); D(Rod) was normal at frequencies between 8 and 12 Hz in all subjects. Rod-driven tCS functions allowed identification of two subgroups of patients: one with band-pass properties and one with low-pass properties, suggesting dominance of different post-receptoral filters. The same filtering properties were observed in L-cone-driven tCS functions. Furthermore, the two subgroups also differed in clinical parameters (spherical equivalent, BCVA, perimetry, and ocular coherence tomography (OCT) reflectivity of the ellipsoid zone relative to the RPE). CONCLUSIONS: OMD was characterized predominantly by deterioration of L- and M-cone-cone driven function in the perifovea. Rod-driven functions were normal. Differences in the photoreceptor signals were further modified by postreceptoral filters. The Association for Research in Vision and Ophthalmology 2023-06-21 /pmc/articles/PMC10289274/ /pubmed/37342031 http://dx.doi.org/10.1167/iovs.64.7.33 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
Huchzermeyer, Cord
Fars, Julien
Kremers, Jan
Kühlewein, Laura
Kempf, Melanie
Ott, Saskia
Stingl, Krunoslav
Stingl, Katarina
Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
title Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
title_full Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
title_fullStr Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
title_full_unstemmed Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
title_short Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
title_sort photoreceptor-specific temporal contrast sensitivities in rp1l1-associated occult macular dystrophy
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289274/
https://www.ncbi.nlm.nih.gov/pubmed/37342031
http://dx.doi.org/10.1167/iovs.64.7.33
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