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Author Spotlight: Ex Vivo OCT-Based Multimodal Imaging of Human Donor Eyes for Research into Age-Related Macular Degeneration
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Retinal asymmetry in multiple sclerosis.

Axel Petzold1,2,3, Sharon Y L Chua4, Anthony P Khawaja4

  • 1Moorfields Eye Hospital and The National Hospital for Neurology and Neurosurgery, London, UK.

Brain : a Journal of Neurology
|November 30, 2020
PubMed
Summary
This summary is machine-generated.

Retinal optical coherence tomography (OCT) asymmetry measures show potential for diagnosing multiple sclerosis (MS). The macular ganglion cell inner plexiform layer (GCIPL) complex demonstrated the highest diagnostic power, though higher sensitivity is needed for clinical viability.

Keywords:
biomarkersdemyelinationimagingmultiple sclerosisoptic neuritis

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Area of Science:

  • Ophthalmology and Neuroscience
  • Medical Imaging and Diagnostics

Background:

  • Multiple sclerosis (MS) diagnosis relies on clinical and paraclinical tests.
  • Retinal optical coherence tomography (OCT) shows promise in detecting MS-related changes.
  • Assessing inter-eye retinal asymmetry via OCT could offer a novel diagnostic approach.

Purpose of the Study:

  • To evaluate the feasibility of using OCT-derived retinal asymmetry measures for diagnosing MS at a community level.
  • To compare the diagnostic performance of different retinal layers and asymmetry metrics (IEPD, IEAD) for MS detection.

Main Methods:

  • Community-based study of 72,120 subjects using UK Biobank data (2007-2010).
  • Calculated inter-eye percentage difference (IEPD) and inter-eye absolute difference (IEAD) for macular RNFL, GCIPL, and ganglion cell complex.
  • Utilized receiver operating characteristic curve (AUROC) analysis to assess discriminatory power, accounting for comorbidities.

Main Results:

  • The macular GCIPL complex showed the highest diagnostic power (AUROC 0.71 for both IEPD and IEAD).
  • Sensitivity for GCIPL complex IEPD (4% cut-off) was 51.7%, and for IEAD (4 µm cut-off) was 43.5%, with specificities of 82.8% and 86.8%.
  • Diagnostic power decreased with increased comorbidities; the metric could not differentiate MS from neuromyelitis optica spectrum disease.

Conclusions:

  • OCT macular GCIPL complex asymmetry (IEPD, IEAD) can serve as a supportive diagnostic measure for MS in young patients without significant comorbidities.
  • Current sensitivity and specificity levels require improvement for widespread clinical adoption.
  • Retinal OCT offers a rapid, non-invasive, and accessible imaging modality that could reduce the need for more invasive diagnostic procedures.