REVIEW article

Front. Neurol.

Sec. Neuro-Ophthalmology

Volume 16 - 2025 | doi: 10.3389/fneur.2025.1559172

Advances in Biomarkers for Optic Neuritis and Neuromyelitis Optica Spectrum Disorders: A Multi-Omics Perspective

Provisionally accepted
Lidong  LiuLidong Liu1Kai  GuoKai Guo2*Dayong  YangDayong Yang1*
  • 1The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Autonomous Region, China
  • 2Mayo Clinic, Rochester, Minnesota, United States

The final, formatted version of the article will be published soon.

Optic neuritis (ON) and neuromyelitis optica spectrum disorders (NMOSD) are inflammatory neuro-ophthalmological conditions characterized by significant visual impairment and diverse clinical manifestations. Advances in diagnostic biomarkers have improved disease identification, including aquaporin-4 immunoglobulin G (AQP4-IgG) and myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG). However, some patients remain biomarker-negative, complicating differential diagnosis and personalized treatment. Multi-omics approaches have provided valuable insights into critical molecular pathways, novel biomarkers, and the shared and distinct features of ON and NMOSD. This review highlights recent advancements in biomarker research for ON and NMOSD, emphasizes the potential of multi-omics integration, identifies existing challenges, and proposes future research directions. These findings aim to enhance diagnostic accuracy, improve prognostic capabilities, and support the development of precision medicine strategies for ON and NMOSD.

Keywords: Optic Neuritis, neuromyelitis optica spectrum disorders, biomarker, multi-omics, AQP4, MOG

Received: 17 Jan 2025; Accepted: 14 Apr 2025.

Copyright: © 2025 Liu, Guo and Yang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Kai Guo, Mayo Clinic, Rochester, 55902, Minnesota, United States
Dayong Yang, The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Autonomous Region, China

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