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The Capital Region of Denmark - a part of Copenhagen University Hospital
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Optical coherence tomography in acute optic neuritis: A population-based study

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  • Kerstin Soelberg
  • Svenja Specovius
  • Hanna G Zimmermann
  • Jakob Grauslund
  • Jesper J Mehlsen
  • Clement Olesen
  • Allan S B Neve
  • Friedemann Paul
  • Alexander U Brandt
  • Nasrin Asgari
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OBJECTIVES: To measure early structural damage caused by autoimmune inflammatory optic neuritis (ON) by optical coherence tomography (OCT) in a population-based cohort.

METHODS: In a prospective population-based study over 24 months in Southern Denmark, patients diagnosed with acute ON and without prior diagnosis of a chronic neuroinflammatory disorder were included and examined with OCT, visual evoked potentials (VEP), visual fields, high contrast visual acuity (HCVA), and low contrast letter acuity (LCLA). Structural and functional outcomes were determined at 6-month follow-up based on interocular differences.

RESULTS: The 50 included patients had on average 16.9 μm peripapillary retinal nerve fiber layer loss, 10.6 μm ganglion cell and inner plexiform layer (GCIP) loss, and an average HCVA decrease of 0.22 dec. Based on a linear regression model, average GCIP loss amounted to -0.2 μm per day and started 8 days after onset. OCT outcomes but not VEP correlated well with all visual function measurements at follow-up. Structural and functional damage in 20 patients (40%) diagnosed de novo with multiple sclerosis (MS) and in 2 patients (4%) with positive myelin oligodendrocyte glycoprotein antibodies (MOG-IgG) test did not differ from patients with idiopathic ON.

CONCLUSIONS: Optic neuritis causes substantial retinal damage and vision loss independent of the underlying disease. Our study supports that GCIP damage starts closely to clinical onset. Good structure-function correlations between OCT and vision support the importance of OCT in monitoring acute ON.

Original languageEnglish
JournalActa Neurologica Scandinavica
Volume138
Issue number6
Pages (from-to)566-573
Number of pages8
ISSN0001-6314
DOIs
Publication statusPublished - Dec 2018

ID: 55739761