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 inInvestigative ophthalmology & visual science Vol. 65; no. 10; p. 45
Main Authors Wendel, Benjamin J., Pandiyan, Vimal Prabhu, Liu, Teng, Jiang, Xiaoyun, Lassoued, Ayoub, Slezak, Emily, Schleufer, Sierra, Bharadwaj, Palash, Tuten, William S., Mustafi, Debarshi, Chao, Jennifer R., Sabesan, Ramkumar
Format Journal Article
LanguageEnglish
Published United States 01.08.2024
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ISSN1552-5783
1552-5783
DOI10.1167/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.
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.
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  surname: Sabesan
  fullname: Sabesan, Ramkumar
  organization: Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington, United States
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Cites_doi 10.1167/iovs.14-15576
10.1167/iovs.13-12557
10.1093/hmg/ddu005
10.1097/OPX.0b013e3182512b98
10.1016/j.cub.2023.03.007
10.1364/BOE.473475
10.1167/iovs.18-25688
10.1364/BOE.7.004899
10.1117/12.3003241
10.3389/fopht.2024.1373549
10.1364/BOE.399034
10.1016/j.preteyeres.2020.100920
10.1007/978-3-030-27378-1_22
10.1364/BOE.436337
10.1080/21678707.2020.1735352
10.1016/j.preteyeres.2018.03.005
10.1167/iovs.09-4945
10.1167/iovs.14-14542
10.1126/sciadv.abc1124
10.1364/OL.398868
10.1167/iovs.61.4.42
10.1073/pnas.1606428113
10.1167/iovs.08-2936
10.1038/nature06150
10.1002/cne.v312:4
10.1038/s41598-023-49338-0
10.1073/pnas.1816360116
10.3758/BF03202828
10.1001/jamaophthalmol.2019.3298
10.1016/j.neuron.2019.02.015
10.1364/OE.409193
10.1371/journal.pone.0079447
10.1167/iovs.15-18246
10.1167/iovs.18-24635
10.1167/iovs.10-5799
10.1017/S095252380001049X
10.1073/pnas.2202485119
10.1016/S0042-6989(01)00043-8
10.1038/343364a0
10.1073/pnas.2107444118
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References Sun (bib4) 2016; 57
Iga (bib35) 2023; 13
Makiyama (bib5) 2013; 8
Lassoued (bib17) 2021; 118
Duncan (bib6) 2019
Dryja (bib1) 1990; 343
Watson (bib22) 1983; 33
Telias (bib34) 2019; 102
Azimipour (bib15) 2020; 45
Sayo (bib28) 2018; 59
Foote (bib9) 2020; 61
Rangaswamy (bib29) 2010; 51
Pandiyan (bib43) 2020; 11
Ratnam (bib7) 2013; 54
Zhang (bib37) 2017; 114
Wang (bib25) 2015; 56
Rodieck (bib23) 1991; 6
Foote (bib30) 2019; 60
Lee (bib32) 2022; 38:110317
Jiang (bib36) 2022; 13
Ji (bib38) 2024
Roorda (bib24) 2001; 41
Gaffney (bib18); 4
Curcio (bib27) 1991; 312
Wynne (bib3) 2021; 83
Scoles (bib21) 2014; 55
Yusuf (bib40) 2019; 137
Zhang (bib12) 2019; 116
Ellis (bib33) 2023; 33
Pandiyan (bib11) 2020; 6
Cooper (bib14) 2020; 28
Tuten (bib8) 2012; 89
Menghini (bib10) 2020; 8
Pandiyan (bib16) 2022; 119
Chen (bib20) 2016; 7
Pandiyan (bib42) 2021; 12
Hood (bib19) 2011; 52
Hood (bib26) 2009; 50
Birch (bib39) 1982; 22
Hillmann (bib13) 2016; 113
Chen (bib41) 2014; 23
Verbakel (bib2) 2018; 66
Dunn (bib31) 2007; 449
References_xml – volume: 56
  start-page: 778
  year: 2015
  ident: bib25
  article-title: Adaptive optics microperimetry and OCT images show preserved function and recovery of cone visibility in macular telangiectasia type 2 retinal lesions
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.14-15576
– volume: 54
  start-page: 5836
  year: 2013
  ident: bib7
  article-title: Relationship between foveal cone structure and clinical measures of visual function in patients with inherited retinal degenerations
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.13-12557
– volume: 23
  start-page: 2926
  year: 2014
  ident: bib41
  article-title: PRPF4 mutations cause autosomal dominant retinitis pigmentosa
  publication-title: Hum Mol Genet
  doi: 10.1093/hmg/ddu005
– volume: 89
  start-page: 563
  year: 2012
  ident: bib8
  article-title: Adaptive optics scanning laser ophthalmoscope-based microperimetry
  publication-title: Optom Vis Sci
  doi: 10.1097/OPX.0b013e3182512b98
– volume: 33
  start-page: 1513
  year: 2023
  ident: bib33
  article-title: Cones and cone pathways remain functional in advanced retinal degeneration
  publication-title: Curr Biol
  doi: 10.1016/j.cub.2023.03.007
– volume: 13
  start-page: 5989
  year: 2022
  ident: bib36
  article-title: Coarse-scale optoretinography (CoORG) with extended field-of-view for normative characterization
  publication-title: Biomed Opt Express
  doi: 10.1364/BOE.473475
– volume: 60
  start-page: 1234
  year: 2019
  ident: bib30
  article-title: Cone spacing correlates with retinal thickness and microperimetry in patients with inherited retinal degenerations
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.18-25688
– volume: 7
  start-page: 4899
  year: 2016
  ident: bib20
  article-title: Multi-modal automatic montaging of adaptive optics retinal images
  publication-title: Biomed Opt Express
  doi: 10.1364/BOE.7.004899
– start-page: 41
  volume-title: Ophthalmic Technologies XXXIV. SPIE
  year: 2024
  ident: bib38
  article-title: Method for assessing structure and function of cone photoreceptors with multiple outer segment reflections in healthy and diseased eyes
  doi: 10.1117/12.3003241
– volume: 4
  start-page: 1373549
  ident: bib18
  article-title: Intensity-based optoretinography reveals sub-clinical deficits in cone function in retinitis pigmentosa
  publication-title: Front Ophthalmol
  doi: 10.3389/fopht.2024.1373549
– volume: 11
  start-page: 5274
  issue: 9
  year: 2020
  ident: bib43
  article-title: High-speed adaptive optics line-scan OCT for cellular-resolution optoretinography
  publication-title: Biomed Opt Express
  doi: 10.1364/BOE.399034
– volume: 83
  start-page: 100920
  year: 2021
  ident: bib3
  article-title: Promises and pitfalls of evaluating photoreceptor-based retinal disease with adaptive optics scanning light ophthalmoscopy (AOSLO)
  publication-title: Prog Retin Eye Res
  doi: 10.1016/j.preteyeres.2020.100920
– start-page: 133
  year: 2019
  ident: bib6
  article-title: Dysflective cones
  publication-title: Adv Exp Med Biol
  doi: 10.1007/978-3-030-27378-1_22
– volume: 12
  start-page: 5865
  issue: 9
  year: 2021
  ident: bib42
  article-title: Reflective mirror-based line-scan adaptive optics OCT for imaging retinal structure and function
  publication-title: Biomed Opt Express
  doi: 10.1364/BOE.436337
– volume: 8
  start-page: 67
  year: 2020
  ident: bib10
  article-title: Monitoring progression of retinitis pigmentosa: current recommendations and recent advances
  publication-title: Exp Opin Orphan Drugs
  doi: 10.1080/21678707.2020.1735352
– volume: 66
  start-page: 157
  year: 2018
  ident: bib2
  article-title: Non-syndromic retinitis pigmentosa
  publication-title: Prog Retin Eye Res
  doi: 10.1016/j.preteyeres.2018.03.005
– volume: 51
  start-page: 4213
  year: 2010
  ident: bib29
  article-title: A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.09-4945
– volume: 55
  start-page: 4244
  year: 2014
  ident: bib21
  article-title: In vivo imaging of human cone photoreceptor inner segments
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.14-14542
– volume: 6
  start-page: eabc1124
  year: 2020
  ident: bib11
  article-title: The optoretinogram reveals the primary steps of phototransduction in the living human eye
  publication-title: Sci Adv
  doi: 10.1126/sciadv.abc1124
– volume: 38:110317
  year: 2022
  ident: bib32
  article-title: Inhibition, but not excitation, recovers from partial cone loss with greater spatiotemporal integration, synapse density, and frequency
  publication-title: Cell Rep
– volume: 45
  start-page: 4658
  year: 2020
  ident: bib15
  article-title: Optoretinogram: optical measurement of human cone and rod photoreceptor responses to light
  publication-title: Opt Lett
  doi: 10.1364/OL.398868
– volume: 114
  start-page: E2937
  year: 2017
  ident: bib37
  article-title: In vivo optophysiology reveals that G-protein activation triggers osmotic swelling and increased light scattering of rod photoreceptors
  publication-title: Proc Natl Acad Sci USA
– volume: 61
  start-page: 42
  year: 2020
  ident: bib9
  article-title: Comparing cone structure and function in RHO- and RPGR-associated retinitis pigmentosa
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.61.4.42
– volume: 113
  start-page: 13138
  year: 2016
  ident: bib13
  article-title: In vivo optical imaging of physiological responses to photostimulation in human photoreceptors
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1606428113
– volume: 50
  start-page: 2328
  year: 2009
  ident: bib26
  article-title: Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.08-2936
– volume: 449
  start-page: 603
  year: 2007
  ident: bib31
  article-title: Light adaptation in cone vision involves switching between receptor and post-receptor sites
  publication-title: Nature
  doi: 10.1038/nature06150
– volume: 22
  start-page: 157
  year: 1982
  ident: bib39
  article-title: The Stiles-Crawford effect in retinitis pigmentosa
  publication-title: Invest Ophthalmol Vis Sci
– volume: 312
  start-page: 610
  year: 1991
  ident: bib27
  article-title: Distribution and morphology of human cone photoreceptors stained with anti-blue opsin
  publication-title: J Comp Neurol
  doi: 10.1002/cne.v312:4
– volume: 13
  start-page: 22040
  year: 2023
  ident: bib35
  article-title: Progression of retinitis pigmentosa on static perimetry, optical coherence tomography, and fundus autofluorescence
  publication-title: Sci Rep
  doi: 10.1038/s41598-023-49338-0
– volume: 116
  start-page: 7951
  year: 2019
  ident: bib12
  article-title: Cone photoreceptor classification in the living human eye from photostimulation-induced phase dynamics
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1816360116
– volume: 33
  start-page: 113
  year: 1983
  ident: bib22
  article-title: QUEST: a Bayesian adaptive psychometric method
  publication-title: Percept Psychophys
  doi: 10.3758/BF03202828
– volume: 137
  start-page: 1295
  year: 2019
  ident: bib40
  article-title: Clinical characterization of retinitis pigmentosa associated with variants in SNRNP200
  publication-title: JAMA Ophthalmol
  doi: 10.1001/jamaophthalmol.2019.3298
– volume: 102
  start-page: 574
  year: 2019
  ident: bib34
  article-title: Retinoic acid induces hyperactivity, and blocking its receptor unmasks light responses and augments vision in retinal degeneration
  publication-title: Neuron
  doi: 10.1016/j.neuron.2019.02.015
– volume: 28
  start-page: 39326
  year: 2020
  ident: bib14
  article-title: Optoretinography of individual human cone photoreceptors
  publication-title: Opt Express
  doi: 10.1364/OE.409193
– volume: 8
  start-page: e79447
  year: 2013
  ident: bib5
  article-title: Macular cone abnormalities in retinitis pigmentosa with preserved central vision using adaptive optics scanning laser ophthalmoscopy
  publication-title: PloS One
  doi: 10.1371/journal.pone.0079447
– volume: 57
  start-page: 2428
  year: 2016
  ident: bib4
  article-title: Assessing photoreceptor structure in retinitis pigmentosa and Usher syndrome
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.15-18246
– volume: 59
  start-page: 3469
  year: 2018
  ident: bib28
  article-title: Significant relationship of visual field sensitivity in central 10 to thickness of retinal layers in retinitis pigmentosa
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.18-24635
– volume: 52
  start-page: 101
  year: 2011
  ident: bib19
  article-title: The transition zone between healthy and diseased retina in patients with retinitis pigmentosa
  publication-title: Invest Ophthalmol Vis Sci
  doi: 10.1167/iovs.10-5799
– volume: 6
  start-page: 95
  year: 1991
  ident: bib23
  article-title: The density recovery profile: a method for the analysis of points in the plane applicable to retinal studies
  publication-title: Vis Neurosci
  doi: 10.1017/S095252380001049X
– volume: 119
  start-page: e2202485119
  year: 2022
  ident: bib16
  article-title: Human cone elongation responses can be explained by photoactivated cone opsin and membrane swelling and osmotic response to phosphate produced by RGS9-catalyzed GTPase
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.2202485119
– volume: 41
  start-page: 1291
  year: 2001
  ident: bib24
  article-title: Packing arrangement of the three cone classes in primate retina
  publication-title: Vis Res
  doi: 10.1016/S0042-6989(01)00043-8
– volume: 343
  start-page: 364
  year: 1990
  ident: bib1
  article-title: A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
  publication-title: Nature
  doi: 10.1038/343364a0
– volume: 118
  start-page: e2107444118
  year: 2021
  ident: bib17
  article-title: Cone photoreceptor dysfunction in retinitis pigmentosa revealed by optoretinography
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.2107444118
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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
Volume 65
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