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Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis

OBJECTIVE: This longitudinal study aimed to assess changes in retinal structure and visual function following a first-ever episode of acute optic neuritis (ON). METHODS: Clinical and optical coherence tomography (OCT) data obtained over a period of 12 months were retrospectively analyzed in 41 patie...

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Autores principales: Wicki, Carla A., Manogaran, Praveena, Simic, Tanja, Hanson, James V.M., Schippling, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051214/
https://www.ncbi.nlm.nih.gov/pubmed/31969471
http://dx.doi.org/10.1212/NXI.0000000000000671
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author Wicki, Carla A.
Manogaran, Praveena
Simic, Tanja
Hanson, James V.M.
Schippling, Sven
author_facet Wicki, Carla A.
Manogaran, Praveena
Simic, Tanja
Hanson, James V.M.
Schippling, Sven
author_sort Wicki, Carla A.
collection PubMed
description OBJECTIVE: This longitudinal study aimed to assess changes in retinal structure and visual function following a first-ever episode of acute optic neuritis (ON). METHODS: Clinical and optical coherence tomography (OCT) data obtained over a period of 12 months were retrospectively analyzed in 41 patients with a first-ever clinical episode of acute ON. OCT scans, high-contrast visual acuity (HCVA), and low-contrast visual acuity (LCVA) were acquired at baseline and at 1, 3, 6, and 12 months thereafter. Macular ganglion cell and inner plexiform layer (GCIP), peripapillary retinal nerve fiber layer (pRNFL), and macular inner nuclear layer (INL) thicknesses were assessed by OCT. Linear mixed-effects models were used to analyze OCT variables of ipsilateral ON and contralateral non-ON (NON) eyes over time. RESULTS: The mean change of GCIP thickness in ON eyes was significant at all follow-up time points, with nearly 75% of the total reduction having occurred by month 1. In ON eyes, thinner GCIP thickness at month 1 correlated with lower LCVA at month 3. Mean pRNFL thickness in ON eyes differed significantly from NON eyes at all postbaseline time points. INL thickness was significantly increased in ON eyes (month 1) but also in contralateral NON eyes (month 12). CONCLUSIONS: Retinal structural damage develops rapidly following acute ON and is associated with subsequent functional visual deficits. Our results also suggest bilateral retinal pathology following unilateral ON, possibly caused by subclinical involvement of the contralateral NON eyes. Moreover, our data may assist in clinical trial planning in studies targeting tissue damage in acute ON.
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spelling pubmed-70512142020-03-13 Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis Wicki, Carla A. Manogaran, Praveena Simic, Tanja Hanson, James V.M. Schippling, Sven Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: This longitudinal study aimed to assess changes in retinal structure and visual function following a first-ever episode of acute optic neuritis (ON). METHODS: Clinical and optical coherence tomography (OCT) data obtained over a period of 12 months were retrospectively analyzed in 41 patients with a first-ever clinical episode of acute ON. OCT scans, high-contrast visual acuity (HCVA), and low-contrast visual acuity (LCVA) were acquired at baseline and at 1, 3, 6, and 12 months thereafter. Macular ganglion cell and inner plexiform layer (GCIP), peripapillary retinal nerve fiber layer (pRNFL), and macular inner nuclear layer (INL) thicknesses were assessed by OCT. Linear mixed-effects models were used to analyze OCT variables of ipsilateral ON and contralateral non-ON (NON) eyes over time. RESULTS: The mean change of GCIP thickness in ON eyes was significant at all follow-up time points, with nearly 75% of the total reduction having occurred by month 1. In ON eyes, thinner GCIP thickness at month 1 correlated with lower LCVA at month 3. Mean pRNFL thickness in ON eyes differed significantly from NON eyes at all postbaseline time points. INL thickness was significantly increased in ON eyes (month 1) but also in contralateral NON eyes (month 12). CONCLUSIONS: Retinal structural damage develops rapidly following acute ON and is associated with subsequent functional visual deficits. Our results also suggest bilateral retinal pathology following unilateral ON, possibly caused by subclinical involvement of the contralateral NON eyes. Moreover, our data may assist in clinical trial planning in studies targeting tissue damage in acute ON. Lippincott Williams & Wilkins 2020-01-22 /pmc/articles/PMC7051214/ /pubmed/31969471 http://dx.doi.org/10.1212/NXI.0000000000000671 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Wicki, Carla A.
Manogaran, Praveena
Simic, Tanja
Hanson, James V.M.
Schippling, Sven
Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
title Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
title_full Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
title_fullStr Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
title_full_unstemmed Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
title_short Bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
title_sort bilateral retinal pathology following a first-ever clinical episode of autoimmune optic neuritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051214/
https://www.ncbi.nlm.nih.gov/pubmed/31969471
http://dx.doi.org/10.1212/NXI.0000000000000671
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