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Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C
INTRODUCTION: Niemann-Pick type C (NPC) is a lysosomal storage disease that is progressive and life-limiting, with an estimated incidence of 1:120,000 live births. In addition to systemic manifestation with (hepato-)splenomegaly, there are a number of neurological manifestations (ataxia, dysarthria,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177533/ https://www.ncbi.nlm.nih.gov/pubmed/34086834 http://dx.doi.org/10.1371/journal.pone.0252825 |
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author | Hopf, Susanne Hennermann, Julia B. Schuster, Alexander K. Pfeiffer, Norbert Pitz, Susanne |
author_facet | Hopf, Susanne Hennermann, Julia B. Schuster, Alexander K. Pfeiffer, Norbert Pitz, Susanne |
author_sort | Hopf, Susanne |
collection | PubMed |
description | INTRODUCTION: Niemann-Pick type C (NPC) is a lysosomal storage disease that is progressive and life-limiting, with an estimated incidence of 1:120,000 live births. In addition to systemic manifestation with (hepato-)splenomegaly, there are a number of neurological manifestations (ataxia, dysarthria, dementia, cataplexy, epileptic seizures, and psychiatric disorders). Characteristic is vertical supranuclear gaze palsy, which is often overlooked. Early diagnosis and start of therapy improve quality of life. This study aimed to characterize oculomotor dysfunction of NPC patients, and to provide ophthalmologic data including retinal imaging. METHODS: Eighteen patients with biochemically or genetically diagnosed NPC completed oculomotor and ophthalmologic examination. Ten of them performed saccadometry by infrared based video-oculography. Saccadic parameters were compared to 100 healthy controls, and were correlated with clinical variables. Another subgroup of eight patients received optical coherence tomography (OCT) of the optic disc and the macula, of which the segmented layers were analysed using a crude linear mixed model, and one adjusted for age, sex, and spherical equivalent. RESULTS: Saccadometry revealed slowed peak velocity compared to controls most evident vertically. Peak velocity correlated negatively with SARA-Score, but correlation with clinical assessment of saccades was not significant. Clinical features in the assessment of vertical saccades were intensive blinking and head movements to initiate gaze changes, and lateral trajectory of the eyes. Macular OCT revealed significant total retinal thinning in the fovea, specifically of the outer nuclear layer and outer retinal layer. Para- and perifoveal retinal thicknesses, as well as peripapillary retinal nerve fibre layer were normal. CONCLUSIONS: Foveal thinning was revealed in NPC. It remains to be shown, whether OCT will prove to be useful to monitor progression. Saccadic impairment reflects CNS involvement and therefore is a parameter to demonstrate the progression of NPC, and potentially also the efficacy of new therapies. Saccadometry, in contrast to clinical investigation, allows the precise evaluation of saccades. |
format | Online Article Text |
id | pubmed-8177533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81775332021-06-07 Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C Hopf, Susanne Hennermann, Julia B. Schuster, Alexander K. Pfeiffer, Norbert Pitz, Susanne PLoS One Research Article INTRODUCTION: Niemann-Pick type C (NPC) is a lysosomal storage disease that is progressive and life-limiting, with an estimated incidence of 1:120,000 live births. In addition to systemic manifestation with (hepato-)splenomegaly, there are a number of neurological manifestations (ataxia, dysarthria, dementia, cataplexy, epileptic seizures, and psychiatric disorders). Characteristic is vertical supranuclear gaze palsy, which is often overlooked. Early diagnosis and start of therapy improve quality of life. This study aimed to characterize oculomotor dysfunction of NPC patients, and to provide ophthalmologic data including retinal imaging. METHODS: Eighteen patients with biochemically or genetically diagnosed NPC completed oculomotor and ophthalmologic examination. Ten of them performed saccadometry by infrared based video-oculography. Saccadic parameters were compared to 100 healthy controls, and were correlated with clinical variables. Another subgroup of eight patients received optical coherence tomography (OCT) of the optic disc and the macula, of which the segmented layers were analysed using a crude linear mixed model, and one adjusted for age, sex, and spherical equivalent. RESULTS: Saccadometry revealed slowed peak velocity compared to controls most evident vertically. Peak velocity correlated negatively with SARA-Score, but correlation with clinical assessment of saccades was not significant. Clinical features in the assessment of vertical saccades were intensive blinking and head movements to initiate gaze changes, and lateral trajectory of the eyes. Macular OCT revealed significant total retinal thinning in the fovea, specifically of the outer nuclear layer and outer retinal layer. Para- and perifoveal retinal thicknesses, as well as peripapillary retinal nerve fibre layer were normal. CONCLUSIONS: Foveal thinning was revealed in NPC. It remains to be shown, whether OCT will prove to be useful to monitor progression. Saccadic impairment reflects CNS involvement and therefore is a parameter to demonstrate the progression of NPC, and potentially also the efficacy of new therapies. Saccadometry, in contrast to clinical investigation, allows the precise evaluation of saccades. Public Library of Science 2021-06-04 /pmc/articles/PMC8177533/ /pubmed/34086834 http://dx.doi.org/10.1371/journal.pone.0252825 Text en © 2021 Hopf et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hopf, Susanne Hennermann, Julia B. Schuster, Alexander K. Pfeiffer, Norbert Pitz, Susanne Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C |
title | Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C |
title_full | Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C |
title_fullStr | Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C |
title_full_unstemmed | Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C |
title_short | Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C |
title_sort | vertical saccadic palsy and foveal retinal thinning in niemann-pick disease type c |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177533/ https://www.ncbi.nlm.nih.gov/pubmed/34086834 http://dx.doi.org/10.1371/journal.pone.0252825 |
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