A multi-regression approach to improve optical coherence tomography diagnostic accuracy in multiple sclerosis patients without previous optic neuritis

Jacqueline Chua, Mihai Bostan, Chi Li, Yin Ci Sim, Inna Bujor, Damon Wong, Bingyao Tan, Xinwen Yao, Florian Schwarzhans, Gerhard Garhöfer, Georg Fischer, Clemens Vass, Cristina Tiu, Ruxandra Pirvulescu, Alina Popa-Cherecheanu*, Leopold Schmetterer

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Background: Optical coherence tomography (OCT) is a retinal imaging system that may improve the diagnosis of multiple sclerosis (MS) persons, but the evidence is currently equivocal. To assess whether compensating the peripapillary retinal nerve fiber layer (pRNFL) thickness for ocular anatomical features as well as the combination with macular layers can improve the capability of OCT in differentiating non-optic neuritis eyes of relapsing-remitting MS patients from healthy controls. Methods: 74 MS participants (n = 129 eyes) and 84 age- and sex-matched healthy controls (n = 149 eyes) were enrolled. Macular ganglion cell complex (mGCC) thickness was extracted and pRNFL measurement was compensated for ocular anatomical factors. Thickness measurements and their corresponding areas under the receiver operating characteristic curves (AUCs) were compared between groups. Results: Participants with MS showed significantly thinner mGCC, measured and compensated pRNFL (p ≤ 0.026). Compensated pRNFL achieved better performance than measured pRNFL for MS differentiation (AUC, 0.75 vs 0.80; p = 0.020). Combining macular and compensated pRNFL parameters provided the best discrimination of MS (AUC = 0.85 vs 0.75; p < 0.001), translating to an average improvement in sensitivity of 24 percent for differentiation of MS individuals. Conclusion: The capability of OCT in MS differentiation is made more robust by accounting OCT scans for individual anatomical differences and incorporating information from both optic disc and macular regions, representing markers of axonal damage and neuronal injury, respectively.

Original languageEnglish
Article number103010
JournalNeuroImage: Clinical
Volume34
DOIs
Publication statusPublished - Jan 2022
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2022 The Author(s)

ASJC Scopus Subject Areas

  • Radiology Nuclear Medicine and imaging
  • Neurology
  • Clinical Neurology
  • Cognitive Neuroscience

Keywords

  • Macular ganglion cell and inner plexiform layer
  • Macular ganglion cell complex
  • Optical coherence tomography
  • Peripapillary retinal nerve fiber layer
  • Relapsing-remitting multiple sclerosis

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