Multimodal High-Resolution Imaging in Retinitis Pigmentosa: A Comparison Between Optoretinography, Cone Density, and Visual Sensitivity
Retinitis pigmentosa (RP), the most common inherited retinal disease, is characterized by progressive photoreceptor degeneration. It remains unknown to what extent surviving photoreceptors transduce light and support vision in RP. To address this, we correlated structure and functional measures usin...
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Published in | Investigative ophthalmology & visual science Vol. 65; no. 10; p. 45 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.08.2024
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ISSN | 1552-5783 1552-5783 |
DOI | 10.1167/iovs.65.10.45 |
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Abstract | Retinitis pigmentosa (RP), the most common inherited retinal disease, is characterized by progressive photoreceptor degeneration. It remains unknown to what extent surviving photoreceptors transduce light and support vision in RP. To address this, we correlated structure and functional measures using adaptive optics scanning laser ophthalmoscopy (AOSLO), adaptive optics microperimetry, and adaptive optics optical coherence tomography (AO-OCT)-based optoretinograms (ORGs).
Four patients with RP were imaged with AOSLO across the visual field covering the transition zone (TZ) of normal to diseased retina. Cone density was estimated in discrete regions spanning the TZ. Visual sensitivity was assessed by measuring increment thresholds for a 3-arcmin stimulus targeted via active eye tracking in AOSLO. ORGs were measured at the same locations using AO-OCT to assess the cones' functional response to a 528 ± 20-nm stimulus. Individual cone outer segment (COS) lengths were measured from AO-OCT in each subject.
Cone density was significantly reduced in patients with RP. Density reduction correlated with TZ location in 3 patients with RP, while a fourth had patches of reduced density throughout the retina. ORG amplitude was reduced in regions of normal and reduced cone density in all patients with RP. ORG response and COS length were positively correlated in controls but not in patients with RP. Despite deficits in cone density and ORG, visual sensitivity remained comparable to controls in three of four patients with RP.
ORG-based measures of retinal dysfunction may precede deficits in cone structure and visual sensitivity. ORG is a sensitive measure of RP disease status and has significant potential to provide insight into disease progression and treatment efficacy. |
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AbstractList | Retinitis pigmentosa (RP), the most common inherited retinal disease, is characterized by progressive photoreceptor degeneration. It remains unknown to what extent surviving photoreceptors transduce light and support vision in RP. To address this, we correlated structure and functional measures using adaptive optics scanning laser ophthalmoscopy (AOSLO), adaptive optics microperimetry, and adaptive optics optical coherence tomography (AO-OCT)-based optoretinograms (ORGs).PurposeRetinitis pigmentosa (RP), the most common inherited retinal disease, is characterized by progressive photoreceptor degeneration. It remains unknown to what extent surviving photoreceptors transduce light and support vision in RP. To address this, we correlated structure and functional measures using adaptive optics scanning laser ophthalmoscopy (AOSLO), adaptive optics microperimetry, and adaptive optics optical coherence tomography (AO-OCT)-based optoretinograms (ORGs).Four patients with RP were imaged with AOSLO across the visual field covering the transition zone (TZ) of normal to diseased retina. Cone density was estimated in discrete regions spanning the TZ. Visual sensitivity was assessed by measuring increment thresholds for a 3-arcmin stimulus targeted via active eye tracking in AOSLO. ORGs were measured at the same locations using AO-OCT to assess the cones' functional response to a 528 ± 20-nm stimulus. Individual cone outer segment (COS) lengths were measured from AO-OCT in each subject.MethodsFour patients with RP were imaged with AOSLO across the visual field covering the transition zone (TZ) of normal to diseased retina. Cone density was estimated in discrete regions spanning the TZ. Visual sensitivity was assessed by measuring increment thresholds for a 3-arcmin stimulus targeted via active eye tracking in AOSLO. ORGs were measured at the same locations using AO-OCT to assess the cones' functional response to a 528 ± 20-nm stimulus. Individual cone outer segment (COS) lengths were measured from AO-OCT in each subject.Cone density was significantly reduced in patients with RP. Density reduction correlated with TZ location in 3 patients with RP, while a fourth had patches of reduced density throughout the retina. ORG amplitude was reduced in regions of normal and reduced cone density in all patients with RP. ORG response and COS length were positively correlated in controls but not in patients with RP. Despite deficits in cone density and ORG, visual sensitivity remained comparable to controls in three of four patients with RP.ResultsCone density was significantly reduced in patients with RP. Density reduction correlated with TZ location in 3 patients with RP, while a fourth had patches of reduced density throughout the retina. ORG amplitude was reduced in regions of normal and reduced cone density in all patients with RP. ORG response and COS length were positively correlated in controls but not in patients with RP. Despite deficits in cone density and ORG, visual sensitivity remained comparable to controls in three of four patients with RP.ORG-based measures of retinal dysfunction may precede deficits in cone structure and visual sensitivity. ORG is a sensitive measure of RP disease status and has significant potential to provide insight into disease progression and treatment efficacy.ConclusionsORG-based measures of retinal dysfunction may precede deficits in cone structure and visual sensitivity. ORG is a sensitive measure of RP disease status and has significant potential to provide insight into disease progression and treatment efficacy. Retinitis pigmentosa (RP), the most common inherited retinal disease, is characterized by progressive photoreceptor degeneration. It remains unknown to what extent surviving photoreceptors transduce light and support vision in RP. To address this, we correlated structure and functional measures using adaptive optics scanning laser ophthalmoscopy (AOSLO), adaptive optics microperimetry, and adaptive optics optical coherence tomography (AO-OCT)-based optoretinograms (ORGs). Four patients with RP were imaged with AOSLO across the visual field covering the transition zone (TZ) of normal to diseased retina. Cone density was estimated in discrete regions spanning the TZ. Visual sensitivity was assessed by measuring increment thresholds for a 3-arcmin stimulus targeted via active eye tracking in AOSLO. ORGs were measured at the same locations using AO-OCT to assess the cones' functional response to a 528 ± 20-nm stimulus. Individual cone outer segment (COS) lengths were measured from AO-OCT in each subject. Cone density was significantly reduced in patients with RP. Density reduction correlated with TZ location in 3 patients with RP, while a fourth had patches of reduced density throughout the retina. ORG amplitude was reduced in regions of normal and reduced cone density in all patients with RP. ORG response and COS length were positively correlated in controls but not in patients with RP. Despite deficits in cone density and ORG, visual sensitivity remained comparable to controls in three of four patients with RP. ORG-based measures of retinal dysfunction may precede deficits in cone structure and visual sensitivity. ORG is a sensitive measure of RP disease status and has significant potential to provide insight into disease progression and treatment efficacy. |
Author | Wendel, Benjamin J. Liu, Teng Jiang, Xiaoyun Tuten, William S. Sabesan, Ramkumar Mustafi, Debarshi Lassoued, Ayoub Bharadwaj, Palash Pandiyan, Vimal Prabhu Schleufer, Sierra Slezak, Emily Chao, Jennifer R. |
Author_xml | – sequence: 1 givenname: Benjamin J. surname: Wendel fullname: Wendel, Benjamin J. organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 2 givenname: Vimal Prabhu surname: Pandiyan fullname: Pandiyan, Vimal Prabhu organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 3 givenname: Teng surname: Liu fullname: Liu, Teng organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 4 givenname: Xiaoyun surname: Jiang fullname: Jiang, Xiaoyun organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 5 givenname: Ayoub surname: Lassoued fullname: Lassoued, Ayoub organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 6 givenname: Emily surname: Slezak fullname: Slezak, Emily organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 7 givenname: Sierra surname: Schleufer fullname: Schleufer, Sierra organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 8 givenname: Palash surname: Bharadwaj fullname: Bharadwaj, Palash organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 9 givenname: William S. surname: Tuten fullname: Tuten, William S. organization: Herbert Wertheim School of Optometry & Vision Science, University of California Berkeley, Berkeley, California, United States – sequence: 10 givenname: Debarshi surname: Mustafi fullname: Mustafi, Debarshi organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States, Seattle Children's Hospital, Seattle, Washington, United States – sequence: 11 givenname: Jennifer R. surname: Chao fullname: Chao, Jennifer R. organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States – sequence: 12 givenname: Ramkumar surname: Sabesan fullname: Sabesan, Ramkumar organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States |
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Snippet | Retinitis pigmentosa (RP), the most common inherited retinal disease, is characterized by progressive photoreceptor degeneration. It remains unknown to what... |
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SubjectTerms | Adult Cell Count Female Humans Male Middle Aged Multimodal Imaging Ophthalmoscopy - methods Retinal Cone Photoreceptor Cells - pathology Retinal Cone Photoreceptor Cells - physiology Retinitis Pigmentosa - diagnosis Retinitis Pigmentosa - physiopathology Tomography, Optical Coherence - methods Visual Acuity - physiology Visual Field Tests - methods Visual Fields - physiology |
Title | Multimodal High-Resolution Imaging in Retinitis Pigmentosa: A Comparison Between Optoretinography, Cone Density, and Visual Sensitivity |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39207297 https://www.proquest.com/docview/3099797678 |
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