ArticleMolecular neurobiology2025
Multi-omics Mendelian Randomization Reveals Immunometabolic Signatures of the Gut Microbiota in Optic Neuritis and the Potential Therapeutic Role of Vitamin B6.
Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Antioxidant vitamin index and risk of age-related macular degeneration: multicenter validation and clinical translation.npj aging · 2026Article
- Integrative Proteogenomic Analysis Identifies Genetically Supported Plasma Proteins, Metabolites, and Pathways in Glaucoma.Investigative ophthalmology & visual science · 2026Article
- Cathepsin H drives hypoxia-associated inflammatory and angiogenic programs in diabetic retinopathy and represents a potential therapeutic target.International journal of biological sciences · 2026Article
- Decoding paraneoplastic neuromyelitis optica: a multi-omics investigation of tumor-driven T and B cell dynamics.Frontiers in immunology · 2025Review
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2 authors.
Funding
Abstract
Optic neuritis (ON) is an inflammatory condition often linked to autoimmune disorders like multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). Despite its low incidence, ON can lead to severe, irreversible visual impairment. Emerging evidence suggests the gut microbiota (GM) may influence ON through complex immune and metabolic pathways, yet the mechanisms remain underexplored. This study employed a multi-omics Mendelian randomization (MR) approach to assess the causal relationships between GM taxa and ON. We analyzed data from extensive genetic and metabolic profiling, examining the causal effect between 473 GM taxa, 731 immune cells/traits, 1400 metabolites, vitamin B6, and ON. Our methodology involved two-sample MR analysis to establish causality and mediation analysis to explore the mechanisms between GM and ON and potential therapeutic strategies. We identified 27 GM taxa with a direct causal relationship to ON risk. Further analysis highlighted three GM taxa with particularly strong associations. Mediation analysis revealed specific metabolic and immune pathways through which these taxa exert their effects, including notable interactions with vitamin B6 metabolism, which appeared to mediate some of these relationships. We found that vitamin B6 could be a potential therapeutic method by acting on GM in ON. This study advances our understanding of the complex etiology of ON and highlights the potential of GM as a target for therapeutic strategies. The significant role of vitamin B6 suggests new avenues for prevention and treatment, emphasizing the need for further research into diet-based interventions.
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