Neurofilament and glial fibrillary acidic protein in multiple sclerosis
- PMID: 15534240
- DOI: 10.1212/01.wnl.0000142988.49341.d1
Neurofilament and glial fibrillary acidic protein in multiple sclerosis
Abstract
Objective: To evaluate levels of neurofilament light (NFL) and glial fibrillary acidic protein (GFAP) in CSF from patients with multiple sclerosis (MS) in relation to clinical progress of the disease.
Methods: CSF levels of NFL and GFAP were determined by sensitive ELISAs in 99 patients with different subtypes of MS, classified in terms of "ongoing relapse" or "clinically stable disease," and 25 control subjects. Levels were compared with paraclinical data such as immunoglobulin G index and inflammatory cell count in the CSF, and the levels were related to Expanded Disability Status Scale score and progression index at clinical follow-up evaluations later in the disease course.
Results: NFL and GFAP levels were elevated in MS patients as compared with control subjects (p < 0.001). The NFL levels were higher at relapses, whereas GFAP levels were unaffected. High NFL levels correlated with progression in patients with an active relapse (r = 0.49; p < 0.01) and in clinically stable patients (r = 0.29; p < 0.05). GFAP correlated to progression in the total patient cohort (r = 0.24; p < 0.05). Moreover, a strong correlation between NFL levels and inflammatory cell counts was evident in the group of patients with an ongoing relapse (r = 0.52; p = 0.001).
Conclusions: CSF levels of neurofilament light and glial fibrillary acidic protein may have prognostic value in multiple sclerosis.
Similar articles
-
Glial fibrillary acidic protein: a potential biomarker for progression in multiple sclerosis.J Neurol. 2011 May;258(5):882-8. doi: 10.1007/s00415-010-5863-2. Epub 2011 Jan 1. J Neurol. 2011. PMID: 21197541
-
Neurofilament light protein and glial fibrillary acidic protein as biological markers in MS.Neurology. 2003 Dec 23;61(12):1720-5. doi: 10.1212/01.wnl.0000098880.19793.b6. Neurology. 2003. PMID: 14694036 Clinical Trial.
-
Cerebrospinal fluid markers of neuronal and glial cell damage to monitor disease activity and predict long-term outcome in patients with autoimmune encephalitis.Eur J Neurol. 2016 Apr;23(4):796-806. doi: 10.1111/ene.12942. Epub 2016 Jan 29. Eur J Neurol. 2016. PMID: 26822123
-
Neurofilament light chain as a biomarker in neuromyelitis optica spectrum disorder: a comprehensive review and integrated analysis with glial fibrillary acidic protein.Neurol Sci. 2024 Mar;45(3):1255-1261. doi: 10.1007/s10072-023-07277-8. Epub 2023 Dec 23. Neurol Sci. 2024. PMID: 38141119 Review.
-
A candidate biomarker of glial fibrillary acidic protein in CSF and blood in differentiating multiple sclerosis and its subtypes: A systematic review and meta-analysis.Mult Scler Relat Disord. 2021 Jun;51:102870. doi: 10.1016/j.msard.2021.102870. Epub 2021 Feb 25. Mult Scler Relat Disord. 2021. PMID: 33819724 Review.
Cited by
-
Recent Advances in Biosensors for Diagnosis of Autoimmune Diseases.Sensors (Basel). 2024 Feb 26;24(5):1510. doi: 10.3390/s24051510. Sensors (Basel). 2024. PMID: 38475046 Free PMC article. Review.
-
Guidance for use of neurofilament light chain as a cerebrospinal fluid and blood biomarker in multiple sclerosis management.EBioMedicine. 2024 Mar;101:104970. doi: 10.1016/j.ebiom.2024.104970. Epub 2024 Feb 13. EBioMedicine. 2024. PMID: 38354532 Free PMC article. Review.
-
Performance Measures and Plasma Biomarker Levels in Patients with Multiple Sclerosis after 14 Days of Fampridine Treatment: An Explorative Study.Int J Mol Sci. 2024 Jan 27;25(3):1592. doi: 10.3390/ijms25031592. Int J Mol Sci. 2024. PMID: 38338871 Free PMC article.
-
Baseline serum neurofilament light chain levels differentiate aggressive from benign forms of relapsing-remitting multiple sclerosis: a 20-year follow-up cohort.J Neurol. 2023 Dec 12. doi: 10.1007/s00415-023-12135-w. Online ahead of print. J Neurol. 2023. PMID: 38085343
-
Clinical Evaluation of Cerebrospinal Fluid p217tau and Neurofilament Light Chain Levels in Patients with Alzheimer's Disease or Other Neurological Diseases.J Alzheimers Dis. 2023;96(4):1623-1638. doi: 10.3233/JAD-230419. J Alzheimers Dis. 2023. PMID: 38007650 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous