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Cerebrospinal fluid neurofilament light chain levels predict visual outcome after optic neuritis.
Modvig, S; Degn, M; Sander, B; Horwitz, H; Wanscher, B; Sellebjerg, F; Frederiksen, J L.
Affiliation
  • Modvig S; The MS Clinic, Department of neurology, Glostrup Hospital, University of Copenhagen, Denmark/Department of Clinical Immunology, Rigshospitalet, University of Copenhagen, Denmark signe.modvig.stausboell@regionh.dk.
  • Degn M; The MS Clinic, Department of Neurology, Glostrup Hospital, University of Copenhagen, Denmark/Department of Diagnostics, Glostrup Hospital, University of Copenhagen, Denmark.
  • Sander B; Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Denmark.
  • Horwitz H; The MS Clinic, Department of Neurology, Glostrup Hospital, University of Copenhagen, Denmark/Department of Clinical Pharmacology, Bispebjerg Hospital, University of Copenhagen, Denmark.
  • Wanscher B; Department of Clinical Neurophysiology, Glostrup Hospital, University of Copenhagen, Denmark.
  • Sellebjerg F; Danish MS Research Centre, Department of Neurology, Rigshospitalet, University of Copenhagen, Denmark.
  • Frederiksen JL; The MS Clinic, Department of Neurology, Glostrup Hospital, University of Copenhagen, Denmark.
Mult Scler ; 22(5): 590-8, 2016 Apr.
Article in En | MEDLINE | ID: mdl-26283696
BACKGROUND: Optic neuritis is a good model for multiple sclerosis relapse, but currently no tests can accurately predict visual outcome. OBJECTIVE: The purpose of this study was to examine whether cerebrospinal fluid (CSF) biomarkers of tissue damage and remodelling (neurofilament light chain (NF-L), myelin basic protein, osteopontin and chitinase-3-like-1) predict visual outcome after optic neuritis. METHODS: We included 47 patients with optic neuritis as a first demyelinating episode. Patients underwent visual tests, optical coherence tomography (OCT), magnetic resonance imaging (MRI) and lumbar puncture. Biomarkers were measured in CSF by enzyme-linked immunosorbent assay (ELISA). Patients were followed up six months after onset and this included visual tests and OCT. Outcome measures were inter-ocular differences in low contrast visual acuity (LCVA), retinal nerve fibre layer (RNFL) and ganglion cell layer+inner plexiform layer (GC-IPL) thicknesses. RESULTS: CSF NF-L levels at onset predicted inter-ocular differences in follow-up LCVA (ß=13.8, p=0.0008), RNFL (ß=5.6, p=0.0004) and GC-IPL (ß=4.0, p=0.0008). The acute-phase GC-IPL thickness also predicted follow-up LCVA (ß=12.9, p=0.0021 for NF-L, ß=-1.1, p=0.0150 for GC-IPL). Complete/incomplete remission was determined based on LCVA from 30 healthy controls. NF-L had a positive predictive value of 91% and an area under the curve (AUC) of 0.79 for incomplete remission. CONCLUSION: CSF NF-L is a promising biomarker of visual outcome after optic neuritis. This could aid neuroprotective/regenerative medical advancements.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retina / Intermediate Filaments / Optic Neuritis / Multiple Sclerosis / Nerve Fibers Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Mult Scler Journal subject: NEUROLOGIA Year: 2016 Document type: Article Affiliation country: Denmark Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retina / Intermediate Filaments / Optic Neuritis / Multiple Sclerosis / Nerve Fibers Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Mult Scler Journal subject: NEUROLOGIA Year: 2016 Document type: Article Affiliation country: Denmark Country of publication: United kingdom