Myelin injury precedes axonal injury and symptomatic onset in multiple sclerosis
- PMID: 41115958
- DOI: 10.1038/s41591-025-04014-w
Myelin injury precedes axonal injury and symptomatic onset in multiple sclerosis
Abstract
The timing of the biological onset of multiple sclerosis (MS) is unclear. We used high-throughput discovery proteomics and samples from presymptomatic patients with MS and matched healthy controls to define the biological neurological onset and characterize the mechanisms involved. Remarkably, evidence of myelin injury was seen ~7 years before the symptomatic onset and preceded evidence of axonal injury by ~1 year. By contrast, astrocyte involvement became evident only at clinical onset. Numerous changes in the serum proteome indicate the involvement of interleukin 3 and nuclear factor kappa B pathways during the presymptomatic stage. Furthermore, people with MS with a previously reported distinct autoantibody signature showed increased immune cell activity compared to those without. We propose a protein biomarker panel that may help distinguish presymptomatic patients with MS from healthy controls, pending validation in future studies. Our findings can help understand the pathophysiology of MS as well as the cascade of central nervous system injury and might facilitate early detection of MS in high-risk people.
© 2025. The Author(s), under exclusive licence to Springer Nature America, Inc.
Conflict of interest statement
Competing interests: A preliminary patent application has been filed for a new method to diagnose presymptomatic multiple sclerosis using protein biomarker panel, as described in this study. The patent application number is 63/750,666, filed on 28 January 2025. A.A. received consultation/speaker fees from Roche, OctaveBio, EMD Serono and Sanofi. F.S. reports a relationship with F. Hoffmann-La Roche Ltd. that includes employment and equity or stocks. E.D.C. is a founder of Survey Genomics. A.J.G. reports research support and grants from NINDS R01 NS105741 R01AG062562 R01AG038791, NMSS RG-1707-28564, All May See, Westridge Foundation, JAMA Neurology, Roche, Pipeline Pharmaceuticals and Cognito Therapeutics. A.J.G. is also an associate editor for JAMA Neurology. S.L.H. currently serves on the scientific advisory boards of Accure, Alector, Annexon and Hinge Bio; previously consulted for BD, Gilead, Moderna, NGM Bio, Nurix Therapeutics and Pheno Therapeutics; previously served on the Board of Directors of Neurona and currently serves as an advisor. S.L.H. also has received nonfinancial support (travel reimbursement and writing support for anti-CD20-therapy-related meetings and presentations) from F. Hoffmann-La Roche and Novartis AG; and has received no personal compensation from any entity that sells or tests therapeutics for MS. The other authors declare no competing interests.
References
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- The changing demographic pattern of multiple sclerosis epidemiology. Lancet Neurol. 9, 520–532 (2020).
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