Subclinical primary retinal pathology in neuromyelitis optica spectrum disorder

In Hye Jeong, Ho Jin Kim, Nam Hee Kim, Kyoung Sook Jeong, Choul Yong Park

Research output: Contribution to journalArticlepeer-review

62 Scopus citations

Abstract

Foveal thickness may be a more sensitive indicator of primary retinal pathology than retinal nerve fiber layer thickness since the fovea contains no or sparse retinal nerve fiber layer, which coalesces into axons of the optic nerve. To our knowledge, few quantitative in vivo studies have investigated foveal thickness. By using optical coherence tomography, we measured foveal thickness to evaluate intrinsic retinal pathology. Seventy-two neuromyelitis optica spectrum disorder patients (99 eyes with optic neuritis and 45 eyes without optic neuritis) and 34 age-matched controls were included. Foveal thinning was observed both in eyes with non-optic neuritis (185.1 µm, p < 0.001) and optic neuritis (185.0 µm, p < 0.001) relative to controls (205.0 µm). Compared to controls, eyes with non-optic neuritis did not have peripapillary retinal nerve fiber layer thinning, but showed foveal thinning (p < 0.001). In neuromyelitis optica spectrum disorder, foveal thickness correlated with 2.5 % low contrast visual acuity, while retinal nerve fiber layer thickness correlated with high or low contrast visual acuity, extended disability status scale, and disease duration. In this study, we observed foveal thinning irrespective of optic neuritis; thus, we believe that subclinical primary retinal pathology, prior to retinal nerve fiber layer thinning, may exist in neuromyelitis optica spectrum disorder.

Original languageEnglish
Pages (from-to)1343-1348
Number of pages6
JournalJournal of Neurology
Volume263
Issue number7
DOIs
StatePublished - 1 Jul 2016

Keywords

  • Fovea thickness
  • Neuromyelitis optica spectrum disorder
  • Optical coherence tomography

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