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Retinal alterations in patients with Lafora disease.

Authors :
Heitkotter H
Linderman RE
Cava JA
Woertz EN
Mastey RR
Summerfelt P
Chui TY
Rosen RB
Patterson EJ
Vincent A
Carroll J
Minassian BA
Source :
American journal of ophthalmology case reports [Am J Ophthalmol Case Rep] 2021 Jun 15; Vol. 23, pp. 101146. Date of Electronic Publication: 2021 Jun 15 (Print Publication: 2021).
Publication Year :
2021

Abstract

Purpose: Lafora disease is a genetic neurodegenerative metabolic disorder caused by insoluble polyglucosan aggregate accumulation throughout the central nervous system and body. The retina is an accessible neural tissue, which may offer alternative methods to assess neurological diseases quickly and noninvasively. In this way, noninvasive imaging may provide a means to characterize neurodegenerative disease, which enables earlier identification and diagnosis of disease and the ability to monitor disease progression. In this study, we sought to characterize the retina of individuals with Lafora disease using non-invasive retinal imaging.<br />Methods: One eye of three individuals with genetically confirmed Lafora disease were imaged with optical coherence tomography (OCT) and adaptive optics scanning light ophthalmoscopy (AOSLO). When possible, OCT volume and line scans were acquired to assess total retinal thickness, ganglion cell-inner plexiform layer thickness, and outer nuclear layer + Henle fiber layer thickness. OCT angiography (OCTA) scans were acquired in one subject at the macula and optic nerve head (ONH). AOSLO was used to characterize the photoreceptor mosaic and examine the retinal nerve fiber layer (RNFL).<br />Results: Two subjects with previous seizure activity demonstrated reduced retinal thickness, while one subject with no apparent symptoms had normal retinal thickness. All other clinical measures, as well as parafoveal cone density, were within normal range. Nummular reflectivity at the level of the RNFL was observed using AOSLO in the macula and near the ONH in all three subjects.<br />Conclusions: This multimodal retinal imaging approach allowed us to observe a number of retinal structural features in all three individuals. Most notably, AOSLO revealed nummular reflectivity within the inner retina of each subject. This phenotype has not been reported previously and may represent a characteristic change produced by the neurodegenerative process.<br />Competing Interests: Mrs. Linderman is a consultant for OptoVue. Dr. Rosen has personal financial interest in Opticology and Guardion, and is a consultant for OptoVue, Boehringer-Ingelheim, Astellas, Genentech-Roche, NanoRetina, OD-OS, Regeneron, and Bayer. Dr. Vincent is a consultant for Adverum Biotechnologies Inc. Dr. Carroll receives financial support from AGTC and OptoVue, is a consultant for MeiraGTX, and has personal financial interest in Translational Imaging Innovations. Dr. Minassian is chief medical advisor to Taysha Gene Therapies. The following authors have no financial disclosures: H.H., J.A.C., E.N.W., R.M., P.S., T.Y.P., and E.J.P.<br /> (© 2021 The Authors.)

Details

Language :
English
ISSN :
2451-9936
Volume :
23
Database :
MEDLINE
Journal :
American journal of ophthalmology case reports
Publication Type :
Academic Journal
Accession number :
34195479
Full Text :
https://doi.org/10.1016/j.ajoc.2021.101146