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Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders

BACKGROUND: Patients with anti-aquaporin-4 antibody seropositive (AQP4-IgG+) neuromyelitis optica spectrum disorders (NMOSDs) frequently suffer from optic neuritis (ON) leading to severe retinal neuroaxonal damage. Further, the relationship of this retinal damage to a primary astrocytopathy in NMOSD...

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Autores principales: Lu, Angelo, Zimmermann, Hanna G, Specovius, Svenja, Motamedi, Seyedamirhosein, Chien, Claudia, Bereuter, Charlotte, Lana-Peixoto, Marco A, Fontenelle, Mariana Andrade, Ashtari, Fereshteh, Kafieh, Rahele, Dehghani, Alireza, Pourazizi, Mohsen, Pandit, Lekha, D'Cunha, Anitha, Kim, Ho Jin, Hyun, Jae-Won, Jung, Su-Kyung, Leocani, Letizia, Pisa, Marco, Radaelli, Marta, Siritho, Sasitorn, May, Eugene F, Tongco, Caryl, De Sèze, Jérôme, Senger, Thomas, Palace, Jacqueline, Roca-Fernández, Adriana, Leite, Maria Isabel, Sharma, Srilakshmi M, Stiebel-Kalish, Hadas, Asgari, Nasrin, Soelberg, Kerstin Kathrine, Martinez-Lapiscina, Elena H, Havla, Joachim, Mao-Draayer, Yang, Rimler, Zoe, Reid, Allyson, Marignier, Romain, Cobo-Calvo, Alvaro, Altintas, Ayse, Tanriverdi, Uygur, Yildirim, Rengin, Aktas, Orhan, Ringelstein, Marius, Albrecht, Philipp, Tavares, Ivan Maynart, Bichuetti, Denis Bernardi, Jacob, Anu, Huda, Saif, Soto de Castillo, Ibis, Petzold, Axel, Green, Ari J, Yeaman, Michael R, Smith, Terry J, Cook, Lawrence, Paul, Friedemann, Brandt, Alexander U, Oertel, Frederike Cosima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785057/
https://www.ncbi.nlm.nih.gov/pubmed/34711650
http://dx.doi.org/10.1136/jnnp-2021-327412
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author Lu, Angelo
Zimmermann, Hanna G
Specovius, Svenja
Motamedi, Seyedamirhosein
Chien, Claudia
Bereuter, Charlotte
Lana-Peixoto, Marco A
Fontenelle, Mariana Andrade
Ashtari, Fereshteh
Kafieh, Rahele
Dehghani, Alireza
Pourazizi, Mohsen
Pandit, Lekha
D'Cunha, Anitha
Kim, Ho Jin
Hyun, Jae-Won
Jung, Su-Kyung
Leocani, Letizia
Pisa, Marco
Radaelli, Marta
Siritho, Sasitorn
May, Eugene F
Tongco, Caryl
De Sèze, Jérôme
Senger, Thomas
Palace, Jacqueline
Roca-Fernández, Adriana
Leite, Maria Isabel
Sharma, Srilakshmi M
Stiebel-Kalish, Hadas
Asgari, Nasrin
Soelberg, Kerstin Kathrine
Martinez-Lapiscina, Elena H
Havla, Joachim
Mao-Draayer, Yang
Rimler, Zoe
Reid, Allyson
Marignier, Romain
Cobo-Calvo, Alvaro
Altintas, Ayse
Tanriverdi, Uygur
Yildirim, Rengin
Aktas, Orhan
Ringelstein, Marius
Albrecht, Philipp
Tavares, Ivan Maynart
Bichuetti, Denis Bernardi
Jacob, Anu
Huda, Saif
Soto de Castillo, Ibis
Petzold, Axel
Green, Ari J
Yeaman, Michael R
Smith, Terry J
Cook, Lawrence
Paul, Friedemann
Brandt, Alexander U
Oertel, Frederike Cosima
author_facet Lu, Angelo
Zimmermann, Hanna G
Specovius, Svenja
Motamedi, Seyedamirhosein
Chien, Claudia
Bereuter, Charlotte
Lana-Peixoto, Marco A
Fontenelle, Mariana Andrade
Ashtari, Fereshteh
Kafieh, Rahele
Dehghani, Alireza
Pourazizi, Mohsen
Pandit, Lekha
D'Cunha, Anitha
Kim, Ho Jin
Hyun, Jae-Won
Jung, Su-Kyung
Leocani, Letizia
Pisa, Marco
Radaelli, Marta
Siritho, Sasitorn
May, Eugene F
Tongco, Caryl
De Sèze, Jérôme
Senger, Thomas
Palace, Jacqueline
Roca-Fernández, Adriana
Leite, Maria Isabel
Sharma, Srilakshmi M
Stiebel-Kalish, Hadas
Asgari, Nasrin
Soelberg, Kerstin Kathrine
Martinez-Lapiscina, Elena H
Havla, Joachim
Mao-Draayer, Yang
Rimler, Zoe
Reid, Allyson
Marignier, Romain
Cobo-Calvo, Alvaro
Altintas, Ayse
Tanriverdi, Uygur
Yildirim, Rengin
Aktas, Orhan
Ringelstein, Marius
Albrecht, Philipp
Tavares, Ivan Maynart
Bichuetti, Denis Bernardi
Jacob, Anu
Huda, Saif
Soto de Castillo, Ibis
Petzold, Axel
Green, Ari J
Yeaman, Michael R
Smith, Terry J
Cook, Lawrence
Paul, Friedemann
Brandt, Alexander U
Oertel, Frederike Cosima
author_sort Lu, Angelo
collection PubMed
description BACKGROUND: Patients with anti-aquaporin-4 antibody seropositive (AQP4-IgG+) neuromyelitis optica spectrum disorders (NMOSDs) frequently suffer from optic neuritis (ON) leading to severe retinal neuroaxonal damage. Further, the relationship of this retinal damage to a primary astrocytopathy in NMOSD is uncertain. Primary astrocytopathy has been suggested to cause ON-independent retinal damage and contribute to changes particularly in the outer plexiform layer (OPL) and outer nuclear layer (ONL), as reported in some earlier studies. However, these were limited in their sample size and contradictory as to the localisation. This study assesses outer retinal layer changes using optical coherence tomography (OCT) in a multicentre cross-sectional cohort. METHOD: 197 patients who were AQP4-IgG+ and 32 myelin-oligodendrocyte-glycoprotein antibody seropositive (MOG-IgG+) patients were enrolled in this study along with 75 healthy controls. Participants underwent neurological examination and OCT with central postprocessing conducted at a single site. RESULTS: No significant thinning of OPL (25.02±2.03 µm) or ONL (61.63±7.04 µm) were observed in patients who were AQP4-IgG+ compared with patients who were MOG-IgG+ with comparable neuroaxonal damage (OPL: 25.10±2.00 µm; ONL: 64.71±7.87 µm) or healthy controls (OPL: 24.58±1.64 µm; ONL: 63.59±5.78 µm). Eyes of patients who were AQP4-IgG+ (19.84±5.09 µm, p=0.027) and MOG-IgG+ (19.82±4.78 µm, p=0.004) with a history of ON showed parafoveal OPL thinning compared with healthy controls (20.99±5.14 µm); this was not observed elsewhere. CONCLUSION: The results suggest that outer retinal layer loss is not a consistent component of retinal astrocytic damage in AQP4-IgG+ NMOSD. Longitudinal studies are necessary to determine if OPL and ONL are damaged in late disease due to retrograde trans-synaptic axonal degeneration and whether outer retinal dysfunction occurs despite any measurable structural correlates.
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spelling pubmed-87850572022-02-04 Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders Lu, Angelo Zimmermann, Hanna G Specovius, Svenja Motamedi, Seyedamirhosein Chien, Claudia Bereuter, Charlotte Lana-Peixoto, Marco A Fontenelle, Mariana Andrade Ashtari, Fereshteh Kafieh, Rahele Dehghani, Alireza Pourazizi, Mohsen Pandit, Lekha D'Cunha, Anitha Kim, Ho Jin Hyun, Jae-Won Jung, Su-Kyung Leocani, Letizia Pisa, Marco Radaelli, Marta Siritho, Sasitorn May, Eugene F Tongco, Caryl De Sèze, Jérôme Senger, Thomas Palace, Jacqueline Roca-Fernández, Adriana Leite, Maria Isabel Sharma, Srilakshmi M Stiebel-Kalish, Hadas Asgari, Nasrin Soelberg, Kerstin Kathrine Martinez-Lapiscina, Elena H Havla, Joachim Mao-Draayer, Yang Rimler, Zoe Reid, Allyson Marignier, Romain Cobo-Calvo, Alvaro Altintas, Ayse Tanriverdi, Uygur Yildirim, Rengin Aktas, Orhan Ringelstein, Marius Albrecht, Philipp Tavares, Ivan Maynart Bichuetti, Denis Bernardi Jacob, Anu Huda, Saif Soto de Castillo, Ibis Petzold, Axel Green, Ari J Yeaman, Michael R Smith, Terry J Cook, Lawrence Paul, Friedemann Brandt, Alexander U Oertel, Frederike Cosima J Neurol Neurosurg Psychiatry Neuro-Inflammation BACKGROUND: Patients with anti-aquaporin-4 antibody seropositive (AQP4-IgG+) neuromyelitis optica spectrum disorders (NMOSDs) frequently suffer from optic neuritis (ON) leading to severe retinal neuroaxonal damage. Further, the relationship of this retinal damage to a primary astrocytopathy in NMOSD is uncertain. Primary astrocytopathy has been suggested to cause ON-independent retinal damage and contribute to changes particularly in the outer plexiform layer (OPL) and outer nuclear layer (ONL), as reported in some earlier studies. However, these were limited in their sample size and contradictory as to the localisation. This study assesses outer retinal layer changes using optical coherence tomography (OCT) in a multicentre cross-sectional cohort. METHOD: 197 patients who were AQP4-IgG+ and 32 myelin-oligodendrocyte-glycoprotein antibody seropositive (MOG-IgG+) patients were enrolled in this study along with 75 healthy controls. Participants underwent neurological examination and OCT with central postprocessing conducted at a single site. RESULTS: No significant thinning of OPL (25.02±2.03 µm) or ONL (61.63±7.04 µm) were observed in patients who were AQP4-IgG+ compared with patients who were MOG-IgG+ with comparable neuroaxonal damage (OPL: 25.10±2.00 µm; ONL: 64.71±7.87 µm) or healthy controls (OPL: 24.58±1.64 µm; ONL: 63.59±5.78 µm). Eyes of patients who were AQP4-IgG+ (19.84±5.09 µm, p=0.027) and MOG-IgG+ (19.82±4.78 µm, p=0.004) with a history of ON showed parafoveal OPL thinning compared with healthy controls (20.99±5.14 µm); this was not observed elsewhere. CONCLUSION: The results suggest that outer retinal layer loss is not a consistent component of retinal astrocytic damage in AQP4-IgG+ NMOSD. Longitudinal studies are necessary to determine if OPL and ONL are damaged in late disease due to retrograde trans-synaptic axonal degeneration and whether outer retinal dysfunction occurs despite any measurable structural correlates. BMJ Publishing Group 2022-02 2021-10-28 /pmc/articles/PMC8785057/ /pubmed/34711650 http://dx.doi.org/10.1136/jnnp-2021-327412 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Neuro-Inflammation
Lu, Angelo
Zimmermann, Hanna G
Specovius, Svenja
Motamedi, Seyedamirhosein
Chien, Claudia
Bereuter, Charlotte
Lana-Peixoto, Marco A
Fontenelle, Mariana Andrade
Ashtari, Fereshteh
Kafieh, Rahele
Dehghani, Alireza
Pourazizi, Mohsen
Pandit, Lekha
D'Cunha, Anitha
Kim, Ho Jin
Hyun, Jae-Won
Jung, Su-Kyung
Leocani, Letizia
Pisa, Marco
Radaelli, Marta
Siritho, Sasitorn
May, Eugene F
Tongco, Caryl
De Sèze, Jérôme
Senger, Thomas
Palace, Jacqueline
Roca-Fernández, Adriana
Leite, Maria Isabel
Sharma, Srilakshmi M
Stiebel-Kalish, Hadas
Asgari, Nasrin
Soelberg, Kerstin Kathrine
Martinez-Lapiscina, Elena H
Havla, Joachim
Mao-Draayer, Yang
Rimler, Zoe
Reid, Allyson
Marignier, Romain
Cobo-Calvo, Alvaro
Altintas, Ayse
Tanriverdi, Uygur
Yildirim, Rengin
Aktas, Orhan
Ringelstein, Marius
Albrecht, Philipp
Tavares, Ivan Maynart
Bichuetti, Denis Bernardi
Jacob, Anu
Huda, Saif
Soto de Castillo, Ibis
Petzold, Axel
Green, Ari J
Yeaman, Michael R
Smith, Terry J
Cook, Lawrence
Paul, Friedemann
Brandt, Alexander U
Oertel, Frederike Cosima
Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders
title Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders
title_full Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders
title_fullStr Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders
title_full_unstemmed Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders
title_short Astrocytic outer retinal layer thinning is not a feature in AQP4-IgG seropositive neuromyelitis optica spectrum disorders
title_sort astrocytic outer retinal layer thinning is not a feature in aqp4-igg seropositive neuromyelitis optica spectrum disorders
topic Neuro-Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785057/
https://www.ncbi.nlm.nih.gov/pubmed/34711650
http://dx.doi.org/10.1136/jnnp-2021-327412
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