dc.contributor.author
Roca‐Fernández, Adriana
dc.contributor.author
Oertel, Frederike Cosima
dc.contributor.author
Yeo, Tianrong
dc.contributor.author
Motamedi, Seyedamirhosein
dc.contributor.author
Probert, Fay
dc.contributor.author
Craner, Matthew J.
dc.contributor.author
Sastre‐Garriga, Jaume
dc.contributor.author
Zimmermann, Hanna G.
dc.contributor.author
Asseyer, Susanna
dc.contributor.author
Kuchling, Joseph
dc.contributor.author
Bellmann‐Strobl, Judith
dc.contributor.author
Ruprecht, Klemens
dc.contributor.author
Leite, Maria Isabel
dc.contributor.author
Paul, Friedemann
dc.contributor.author
Brandt, Alexander Ulrich
dc.contributor.author
Palace, Jacqueline
dc.date.accessioned
2022-11-24T13:10:36Z
dc.date.available
2022-11-24T13:10:36Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/37015
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-36728
dc.description.abstract
Background and purpose: Foveal changes were reported in aquaporin-4 antibody (AQP4-Ab) seropositive neuromyelitis optica spectrum disorder (NMOSD) patients; however, it is unclear whether they are independent of optic neuritis (ON), stem from subclinical ON or crossover from ON in fellow eyes. Fovea morphometry and a statistical classification approach were used to investigate if foveal changes in NMOSD are independent of ON and progressive.
Methods: This was a retrospective longitudinal study of 27 AQP4-IgG + NMOSD patients (49 eyes; 15 ON eyes and 34 eyes without a history of ON [NON eyes]), follow-up median (first and third quartile) 2.32 (1.33-3.28), and 38 healthy controls (HCs) (76 eyes), follow-up median (first and third quartile) 1.95 (1.83-2.54). The peripapillary retinal nerve fibre layer thickness and the volume of combined ganglion cell and inner plexiform layer as measures of neuroaxonal damage from ON were determined by optical coherence tomography. Nineteen foveal morphometry parameters were extracted from macular optical coherence tomography volume scans. Data were analysed using orthogonal partial least squares discriminant analysis and linear mixed effects models.
Results: At baseline, foveal shape was significantly altered in ON eyes and NON eyes compared to HCs. Discriminatory analysis showed 81% accuracy distinguishing ON vs. HCs and 68% accuracy in NON vs. HCs. NON eyes were distinguished from HCs by foveal shape parameters indicating widening. Orthogonal partial least squares discriminant analysis discriminated ON vs. NON with 76% accuracy. In a follow-up of 2.4 (20.85) years, no significant time-dependent foveal changes were found.
Conclusion: The parafoveal area is altered in AQP4-Ab seropositive NMOSD patients suggesting independent neuroaxonal damage from subclinical ON. Longer follow-ups are needed to confirm the stability of the parafoveal structure over time.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
aquaporin-4 antibodies (AQP4-IgG)
en
dc.subject
foveal morphometry
en
dc.subject
neuromyelitis optica spectrum disorders (NMOSD)
en
dc.subject
optic neuritis
en
dc.subject
retinal neuroaxonal damage
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Foveal changes in aquaporin‐4 antibody seropositive neuromyelitis optica spectrum disorder are independent of optic neuritis and not overtly progressive
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1111/ene.14766
dcterms.bibliographicCitation.journaltitle
European Journal of Neurology
dcterms.bibliographicCitation.number
7
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.pagestart
2280
dcterms.bibliographicCitation.pageend
2293
dcterms.bibliographicCitation.volume
28
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33547839
dcterms.isPartOf.issn
1351-5101
dcterms.isPartOf.eissn
1468-1331