Abstract

PurposeTo assess macular photoreceptor abnormalities in eyes with retinitis pigmentosa (RP) with preserved central vision using adaptive optics scanning laser ophthalmoscopy (AO-SLO).MethodsFourteen eyes of 14 patients with RP (best-corrected visual acuity 20/20 or better) and 12 eyes of 12 volunteers underwent a full ophthalmologic examination, fundus autofluorescence, spectral-domain optical coherence tomography (SD-OCT), and imaging with a prototype AO-SLO system. Cone density and spatial organization of the cone mosaic were assessed using AO-SLO images.ResultsIn 3 eyes with RP and preserved central vision, cones formed a mostly regular mosaic pattern with small patchy dark areas, and in 10 eyes, the cone mosaic patterns were less regular, and large dark regions with missing cones were apparent. Only one eye with RP demonstrated a normal, regular cone mosaic pattern. In eyes with RP, cone density was significantly lower at 0.5 mm and 1.0 mm from the center of the fovea compared to normal eyes (P<0.001 and 0.021, respectively). At 0.5 mm and 1.0 mm from the center of the fovea, a decreased number of cones had 6 neighbors in eyes with RP (P = 0.002 for both). Greater decrease in cone density was related to disruption of the photoreceptor inner segment (IS) ellipsoid band on SD-OCT images (P = 0.044); however, dark regions were seen on AO-SLO even in areas of continuous IS ellipsoid on SD-OCT. Decreased cone density correlated thinner outer nuclear layer (P = 0.029) and thinner inner segment and outer segment thickness (P = 0.011) on SD-OCT.ConclusionsCone density is decreased and the regularity of the cone mosaic spatial arrangement is disrupted in eyes with RP, even when visual acuity and foveal sensitivity are good. AO-SLO imaging is a sensitive quantitative tool for detecting photoreceptor abnormalities in eyes with RP.

Highlights

  • Retinitis pigmentosa (RP), the prevalence of which has been reported as approximately 1:4,000 worldwide, is the term used for a group of disorders that are characterized by inherited, progressive dysfunction and dystrophy of retinal tissue [1,2]

  • Adaptive Optics Scanning Laser Ophthalmoscopy System We have developed an original prototype adaptive optics scanning laser ophthalmoscopy (AO-scanning laser ophthalmoscopy (SLO)) system in collaboration with Canon Inc [34,35]

  • The amplitude did not decrease below the threshold level (1 mV for flicker ERG according to ISCEV protocol and 0.05 mV for focal macula ERG) in any eyes

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Summary

Introduction

Retinitis pigmentosa (RP), the prevalence of which has been reported as approximately 1:4,000 worldwide, is the term used for a group of disorders that are characterized by inherited, progressive dysfunction and dystrophy of retinal tissue [1,2]. Initial involvement of photoreceptors leads to subsequent damage to inner retinal cells. The age of onset of visual impairment in the different types of RP ranges from infancy to late adulthood. Visual impairment usually manifests as night blindness and visual field loss. The eventual visual burden from retinal dystrophy can range from just sectorial visual field loss to profound loss of the peripheral visual field. Central vision may be well preserved even if electroretinography (ERG) shows remarkably reduced response [3]

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