dc.contributor.author
Oertel, Frederike C.
dc.contributor.author
Outteryck, Olivier
dc.contributor.author
Knier, Benjamin
dc.contributor.author
Zimmermann, Hanna
dc.contributor.author
Borisow, Nadja
dc.contributor.author
Bellmann-Strobl, Judith
dc.contributor.author
Blaschek, Astrid
dc.contributor.author
Jarius, Sven
dc.contributor.author
Reindl, Markus
dc.contributor.author
Ruprecht, Klemens
dc.contributor.author
Meinl, Edgar
dc.contributor.author
Hohlfeld, Reinhard
dc.contributor.author
Paul, Friedemann
dc.contributor.author
Brandt, Alexander U.
dc.contributor.author
Kümpfel, Tania
dc.contributor.author
Havla, Joachim
dc.date.accessioned
2019-08-06T09:51:45Z
dc.date.available
2019-08-06T09:51:45Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/25230
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-3935
dc.description.abstract
BACKGROUND: Serum antibodies against myelin-oligodendrocyte-glycoprotein (MOG-IgG) are detectable in a proportion of patients with acute or relapsing neuroinflammation. It is unclear, if neuro-axonal damage occurs only in an attack-dependent manner or also progressively. Therefore, this study aimed to investigate longitudinally intra-retinal layer changes in eyes without new optic neuritis (ON) in MOG-IgG-seropositive patients.
METHODS: We included 38 eyes of 24 patients without ON during follow-up (F/U) [median years (IQR)] 1.9 (1.0-2.2) and 56 eyes of 28 age- and sex-matched healthy controls (HC). The patient group's eyes included 18 eyes without (EyeON-) and 20 eyes with history of ON (EyeON+). Using spectral domain optical coherence tomography (OCT), we acquired peripapillary retinal nerve fiber layer thickness (pRNFL) and volumes of combined ganglion cell and inner plexiform layer (GCIP), inner nuclear layer (INL), and macular volume (MV). High-contrast visual acuity (VA) was assessed at baseline.
RESULTS: At baseline in EyeON-, pRNFL (94.3 ± 15.9 μm, p = 0.36), INL (0.26 ± 0.03 mm3, p = 0.11), and MV (2.34 ± 0.11 mm3, p = 0.29) were not reduced compared to HC; GCIP showed thinning (0.57 ± 0.07 mm3; p = 0.008), and VA was reduced (logMAR 0.05 ± 0.15 vs. - 0.09 ± 0.14, p = 0.008) in comparison to HC. Longitudinally, we observed pRNFL thinning in models including all patient eyes (annual reduction - 2.20 ± 4.29 μm vs. - 0.35 ± 1.17 μm, p = 0.009) in comparison to HC. Twelve EyeON- with other than ipsilateral ON attacks ≤ 6 months before baseline showed thicker pRNFL at baseline and more severe pRNFL thinning in comparison to 6 EyeON- without other clinical relapses.
CONCLUSIONS: We observed pRNFL thinning in patients with MOG-IgG during F/U, which was not accompanied by progressive GCIP reduction. This effect could be caused by a small number of EyeON- with other than ipsilateral ON attacks within 6 months before baseline. One possible interpretation could be a reduction of the swelling, which could mean that MOG-IgG patients show immune-related swelling in the CNS also outside of an attack's target area.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Optical coherence tomography
en
dc.subject
Optic neuritis
en
dc.subject
Myelin-oligodendrocyte-glycoprotein
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Optical coherence tomography in myelin-oligodendrocyte-glycoprotein antibody-seropositive patients: a longitudinal study
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
154
dcterms.bibliographicCitation.doi
10.1186/s12974-019-1521-5
dcterms.bibliographicCitation.journaltitle
Journal of Neuroinflammation
dcterms.bibliographicCitation.originalpublishername
BMC
dcterms.bibliographicCitation.volume
16
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
31345223
dcterms.isPartOf.eissn
1742-2094