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CSF neurofilament light chain testing as an aid to determine treatment strategies in MS.
Reyes, Saúl; Smets, Ide; Holden, David; Carrillo-Loza, Karina; Christmas, Tatiana; Bianchi, Lucia; Ammoscato, Francesca; Turner, Benjamin; Marta, Monica; Schmierer, Klaus; Giovannoni, Gavin; Gnanapavan, Sharmilee.
Afiliación
  • Reyes S; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Smets I; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Holden D; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Carrillo-Loza K; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Christmas T; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Bianchi L; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Ammoscato F; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Turner B; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Marta M; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Schmierer K; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Giovannoni G; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
  • Gnanapavan S; From the The Blizard Institute (S.R., I.S., D.H., K.C.-L., T.C., L.B., F.A., M.M., K.S., G.G., S.G.), Centre for Neuroscience, Surgery & Trauma, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; and Clinical Board Medicine (Neuroscience) (S.R., I.S., B.T., M
Article en En | MEDLINE | ID: mdl-32826298
ABSTRACT

OBJECTIVE:

To evaluate the use of CSF neurofilament light chain (NfL) measurements in clinical practice as well as their effect on treatment strategies and outcomes in patients with MS.

METHODS:

This was an observational cohort study of patients with MS who had a CSF NfL measurement between December 2015 and July 2018 as part of their routine clinical care. Treatment strategies were classified as "No Treatment/No Escalation" (no treatment or no escalation of treatment) or "Treatment/Escalation" (first-line injectable/oral disease-modifying therapies (DMTs), highly active DMTs, or treatment escalation). Change in Expanded Disability Status Scale (EDSS) scores was evaluated after 1-year follow-up.

RESULTS:

Of 203 patients with MS, 117 (58%) had relapsing-remitting MS. Disease activity was most frequently indicated by elevated CSF NfL (n = 85), followed by clinical (n = 81) and MRI activity (n = 65). CSF NfL measurements were independently associated with clinical (p = 0.02) and MRI activity (p < 0.001). Of those with elevated CSF NfL as the only evidence of disease activity (n = 22), 77% had progressive MS (PMS). In patients with PMS, 17 (20%) had elevated CSF NfL as the sole indicator of disease activity. Elevated CSF NfL resulted more frequently in Treatment/Escalation than normal CSF NfL (p < 0.001). Median EDSS change at follow-up was similar between patients receiving No Treatment/No Escalation and Treatment/Escalation decisions (p = 0.81).

CONCLUSIONS:

CSF NfL measurements informed treatment strategies, alongside clinical and MRI measures. CSF NfL levels were the only indicator of disease activity in a subset of patients, which was more pronounced in patients with PMS. Elevated CSF NfL was associated with more Treatment/Escalation strategies, which had an impact on EDSS outcomes at 1 year.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas de Neurofilamentos / Esclerosis Múltiple Crónica Progresiva / Esclerosis Múltiple Recurrente-Remitente / Factores Inmunológicos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Neurol Neuroimmunol Neuroinflamm Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas de Neurofilamentos / Esclerosis Múltiple Crónica Progresiva / Esclerosis Múltiple Recurrente-Remitente / Factores Inmunológicos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Neurol Neuroimmunol Neuroinflamm Año: 2020 Tipo del documento: Article