Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Cellular analysis of retinal pigment epithelium and photoreceptors by transscleral optical imaging in inherited macular dystrophies
Author Affiliations & Notes
  • Andrea Cusumano
    Ophthalmology, Universita degli Studi di Roma Tor Vergata Facolta di Medicina e Chirurgia, Roma, Lazio, Italy
    Macula & Genoma Foundation, Rome, Lazio, Italy
  • Francesco Martelli
    Istituto Superiore di Sanita, Roma, Lazio, Italy
  • Marco Lombardo
    Ophthalmology, Universita degli Studi di Roma Tor Vergata Facolta di Medicina e Chirurgia, Roma, Lazio, Italy
  • Fabian D'Apolito
    Macula & Genoma Foundation, Rome, Lazio, Italy
  • Jacopo Sebastiani
    Macula & Genoma Foundation, Rome, Lazio, Italy
  • Michele D'Ambrosio
    Macula & Genoma Foundation, Rome, Lazio, Italy
  • Matteo Guelpa
    Macula & Genoma Foundation, Rome, Lazio, Italy
  • Benedetto Falsini
    Macula & Genoma Foundation, Rome, Lazio, Italy
  • Footnotes
    Commercial Relationships   Andrea Cusumano None; Francesco Martelli None; Marco Lombardo None; Fabian D'Apolito None; Jacopo Sebastiani None; Michele D'Ambrosio None; Matteo Guelpa None; Benedetto Falsini None
  • Footnotes
    Support  Macula & Genoma Foundation
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 3409. doi:
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      Andrea Cusumano, Francesco Martelli, Marco Lombardo, Fabian D'Apolito, Jacopo Sebastiani, Michele D'Ambrosio, Matteo Guelpa, Benedetto Falsini; Cellular analysis of retinal pigment epithelium and photoreceptors by transscleral optical imaging in inherited macular dystrophies. Invest. Ophthalmol. Vis. Sci. 2024;65(7):3409.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Adaptative Optics Transscleral Flood Illumination (AO-TFI) is a new technology 1 that allows studying retinal structure in vivo, providing cellular level images of the retina. The aim of this study was to evaluate cellular images in patients with inherited macular dystrophy.

Methods : Macular AO-TFI images (FOV of 6.7° x 6.7°) were acquired using Cellularis Discovery (EarlySight SA, Geneva, Switzerland). Quantitative analyses using proprietary software were performed to capture the hyper-reflectivity of the photoreceptor (PR) and the hypo-reflectivity of the retinal pigment epithelium (RPE). Descriptive statistics were then employed to compare PR and RPE characteristics between healthy and IRDs. Four patients with macular dystrophy related to ABCA4 (n = 3) or CDHR1 (n= 1) were included in the study. Multimodal imaging and visual function tests were obtained from all patients.

Results : In ABCA4 patients, RPE cell density measured with Voronoi ranged 527-4005 cell/mm2 (versus normal mean 4887 cell/mm2 SD 454), hyper-reflective regions at the PR layer ranged 472-1720 cell/mm2 (versus normal mean 30000 cell mm2). In CDHR1, l hypo reflective regions at the RPE layer ranged 727-902 cell/mm2, macular cones ranged 511-561 cell/mm2.

Conclusions : By using Cellularis, foveal RPE cells are observed and quantified, macular cones are observed and quantified. Quantification of hypo reflective regions for RPE layer and hyper reflective regions for PR layer could be a mean to compare healthy vs non healthy when Voronoi analysis cannot be used.

1 Kowalczuk L, Dornier R, Kunzi M, et al. In Vivo Retinal Pigment Epithelium Imaging using Transscleral Optical Imaging in Healthy Eyes. Ophthalmol Sci. 2022 Oct 19;3(1):100234.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

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