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ArticleNeurology(R) neuroimmunology & neuroinflammation2026

Ganglion Cell Layer Compared With Inner Plexiform Layer Atrophy After Optic Neuritis Associated With NMOSD, MOGAD, and MS.

Angeliki G Filippatou, Georgios Gakis, Anna Bacchetti, Anna Kim, Yana Said, Brenna McCormack, Ting-Yi Lin, Adam Didouchevski, Nicole Pellegrini, Kathryn C Fitzgerald and 3 more

Abstract readComparative Study
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Angeliki G FilippatouFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0003-0419-233X
Georgios GakisFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-7339-4659
Anna BacchettiFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0009-0000-9434-8531
Anna KimFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0009-0002-1188-5345
Yana SaidFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0009-0004-4350-1910
Brenna McCormackFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0009-0002-6678-7021
Ting-Yi LinFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0001-9605-8095
Adam DidouchevskiFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0009-0009-1993-9513
Nicole PellegriniFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-7181-2562
Kathryn C FitzgeraldFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0003-3137-0322
Peter A CalabresiFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-7776-6472
Shiv SaidhaFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0001-6387-0714
Elias S SotirchosFrom the Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-8812-1637

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesOptic neuritis (ON) is a common manifestation of multiple sclerosis (MS), aquaporin-4-IgG seropositive neuromyelitis optica spectrum disorder (AQP4+NMOSD), and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). Compared with MS-ON, AQP4-ON and MOGAD-ON eyes exhibit more severe thinning of the macular composite ganglion cell + inner plexiform layer (GCIPL), as measured by optical coherence tomography (OCT). The individual measurement of the ganglion cell (GCL) and inner plexiform (IPL) layers, typically assessed together as the composite GCIPL thickness, has remained largely unexplored. In this study, we aimed to examine the relative contribution of GCL and IPL thinning to overall GCIPL thinning in MS-ON, AQP4-ON, and MOGAD-ON eyes.

methodsFor the cross-sectional analysis, MS, AQP4+NMOSD, and MOGAD participants with a history of ON >6 months prior and healthy controls (HC) underwent retinal imaging. For the longitudinal analysis, the evolution of GCL and IPL thinning was examined in people with baseline OCT within 30 days of a first episode of acute ON.

resultsIn the cross-sectional cohort, GCL and IPL volumes were lower in AQP4-ON (n = 30 eyes) and MOGAD-ON (n = 47 eyes), as compared with MS-ON (n = 66 eyes), but did not differ between AQP4-ON and MOGAD-ON eyes. The GCL/GCIPL ratio was lower in ON eyes relative to HC and was correlated with GCIPL volume, with a similar pattern across disease groups. AQP4-ON and MOGAD-ON eyes had a lower GCL/GCIPL ratio compared with MS-ON, with no significant difference between AQP4-ON and MOGAD-ON. In the longitudinal cohort, the GCL/GCIPL ratio was already reduced in the ON eyes (n = 19 eyes) compared with the fellow non-ON eyes at the baseline scan within the first month from ON (-1.01% [-1.59% to -0.44%], DISCUSSION: More severe GCIPL thinning after ON was associated with a lower GCL/GCIPL ratio, supporting that more GCL than IPL thinning occurs after ON. The pattern was similar across neuroinflammatory conditions including MS, MOGAD, and AQP4+NMOSD. Our findings may help shed light into dynamics of inner retinal layer atrophy after ON.

Indexed as

Multiple SclerosisMyelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseNeuromyelitis OpticaOptic NeuritisRetinal Ganglion CellsAdultAquaporin 4AtrophyCross-Sectional StudiesFemaleHumansMaleMiddle AgedMyelin-Oligodendrocyte GlycoproteinTomography, Optical CoherenceAquaporin 4Myelin-Oligodendrocyte Glycoprotein

Identifiers

PMID41881459
PMCPMC13020555

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.