UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Deep phenotyping of PROM1-associated retinal degeneration

Schließleder, Gernot; Kalitzeos, Angelos; Kasilian, Melissa; Singh, Navjit; Wang, Ziyuan; Hu, Zhihong; Großpötzl, Manuel; ... Strauss, Rupert W; + view all (2023) Deep phenotyping of PROM1-associated retinal degeneration. British Journal of Ophthalmology 10.1136/bjo-2022-322036. Green open access

[thumbnail of Kalitzeos_Prom1_phenotyping_BJO_R1v5_figures.pdf]
Preview
Text
Kalitzeos_Prom1_phenotyping_BJO_R1v5_figures.pdf

Download (1MB) | Preview
[thumbnail of Kalitzeos_Prom1_phenotyping_BJO_R1v5_plain text.pdf]
Preview
Text
Kalitzeos_Prom1_phenotyping_BJO_R1v5_plain text.pdf

Download (335kB) | Preview

Abstract

BACKGROUND/AIMS: The purpose of this study was to investigate retinal structure in detail of subjects with autosomal-dominant (AD) and autosomal-recessive (AR) PROM1-associated retinal degeneration (PROM1-RD), study design: institutional, cross-sectional study. METHODS: Four eyes from four subjects (three with AD and one with AR) PROM1-RD were investigated by ophthalmic examination including best-corrected visual acuity (BCVA) and multimodal retinal imaging: fundus autofluorescence (FAF), spectral-domain optical coherence tomography (SD-OCT) and adaptive optics scanning light ophthalmoscopy. Quantitative assessment of atrophic lesions determined by FAF, thickness of individual retinal layers and cone photoreceptor quantification was performed. RESULTS: BCVA ranged from 20/16 to 20/200. Initial pathological changes included the presence of hyperautofluorescent spots on FAF imaging, while later stages demonstrated discrete areas of atrophy. In all patients, thinning of the outer retinal layers on SD-OCT with varying degrees of atrophy could be detected depending on disease-causing variants and age. Cone density was quantified both in central and/or at different eccentricities from the fovea. Longitudinal assessments were possible in two patients. CONCLUSIONS: PROM1-RD comprises a wide range of clinical phenotypes. Depending on the stage of disease, the cone mosaic in PROM1-RD is relatively preserved and can potentially be targeted by cone-directed interventions.

Type: Article
Title: Deep phenotyping of PROM1-associated retinal degeneration
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1136/bjo-2022-322036
Publisher version: http://doi.org/10.1136/bjo-2022-322036
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Ophthalmology
URI: https://discovery.ucl.ac.uk/id/eprint/10169858
Downloads since deposit
117Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item