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Associations of sNfL with clinico-radiological measures in a large MS population.
Sotirchos, Elias S; Fitzgerald, Kathryn C; Singh, Carol M; Smith, Matthew D; Reyes-Mantilla, Maria; Hersh, Carrie M; Hyland, Megan H; Canissario, Ryan; Simmons, Sarah B; Arrambide, Georgina; Montalban, Xavier; Comabella, Manuel; Naismith, Robert T; Qiao, Min; Krupp, Lauren B; Nicholas, Jacqueline A; Akgün, Katja; Ziemssen, Tjalf; Rudick, Richard; Fisher, Elizabeth; Bermel, Robert A; Mowry, Ellen M; Calabresi, Peter A.
Afiliação
  • Sotirchos ES; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Fitzgerald KC; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Singh CM; Biogen, Cambridge, Massachusetts, USA.
  • Smith MD; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Reyes-Mantilla M; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Hersh CM; Lou Ruvo Center for Brain Health, Cleveland Clinic, Las Vegas, Nevada, USA.
  • Hyland MH; Department of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
  • Canissario R; Department of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
  • Simmons SB; Mellen Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Arrambide G; Department of Neurology and Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Montalban X; Department of Neurology and Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Comabella M; Department of Neurology and Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Naismith RT; Department of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
  • Qiao M; Department of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
  • Krupp LB; Department of Neurology, New York University, New York City, New York, USA.
  • Nicholas JA; OhioHealth Multiple Sclerosis Center, Riverside Methodist Hospital, Columbus, Ohio, USA.
  • Akgün K; Center of Clinical Neuroscience, Department of Neurology, University Clinic Carl-Gustav Carus, Dresden, Germany.
  • Ziemssen T; Center of Clinical Neuroscience, Department of Neurology, University Clinic Carl-Gustav Carus, Dresden, Germany.
  • Rudick R; (formerly) Biogen, Cambridge, Massachusetts, USA.
  • Fisher E; Biogen, Cambridge, Massachusetts, USA.
  • Bermel RA; Mellen Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Mowry EM; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Calabresi PA; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Ann Clin Transl Neurol ; 10(1): 84-97, 2023 01.
Article em En | MEDLINE | ID: mdl-36427295
OBJECTIVE: Evaluation of serum neurofilament light chain (sNfL), measured using high-throughput assays on widely accessible platforms in large, real-world MS populations, is a critical step for sNfL to be utilized in clinical practice. METHODS: Multiple Sclerosis Partners Advancing Technology and Health Solutions (MS PATHS) is a network of healthcare institutions in the United States and Europe collecting standardized clinical/imaging data and biospecimens during routine clinic visits. sNfL was measured in 6974 MS and 201 healthy control (HC) participants, using a high-throughput, scalable immunoassay. RESULTS: Elevated sNfL levels for age (sNfL-E) were found in 1238 MS participants (17.8%). Factors associated with sNfL-E included male sex, younger age, progressive disease subtype, diabetes mellitus, impaired renal function, and active smoking. Higher body mass index (BMI) was associated with lower odds of elevated sNfL. Active treatment with disease-modifying therapy was associated with lower odds of sNfL-E. MS participants with sNfL-E exhibited worse neurological function (patient-reported disability, walking speed, manual dexterity, and cognitive processing speed), lower brain parenchymal fraction, and higher T2 lesion volume. Longitudinal analyses revealed accelerated short-term rates of whole brain atrophy in sNfL-E participants and higher odds of new T2 lesion development, although both MS participants with or without sNfL-E exhibited faster rates of whole brain atrophy compared to HC. Findings were consistent in analyses examining age-normative sNfL Z-scores as a continuous variable. INTERPRETATION: Elevated sNfL is associated with clinical disability, inflammatory disease activity, and whole brain atrophy in MS, but interpretation needs to account for comorbidities including impaired renal function, diabetes, and smoking.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo Tipo de estudo: Guideline / Risk_factors_studies Limite: Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo Tipo de estudo: Guideline / Risk_factors_studies Limite: Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article