Your browser doesn't support javascript.
loading
Serum neurofilament light chain cut-off definition for clinical diagnosis and prognosis of amyotrophic lateral sclerosis.
Brousse, Mehdi; Delaby, Constance; De La Cruz, Elisa; Kuhle, Jens; Benkert, Pascal; Mondesert, Etienne; Ginestet, Nelly; Hirtz, Christophe; Camu, William; Lehmann, Sylvain; Esselin, Florence.
Afiliação
  • Brousse M; LBPC-PPC, Université Montpellier, CHU Montpellier, INM INSERM, Montpellier, France.
  • Delaby C; LBPC-PPC, Université Montpellier, CHU Montpellier, INM INSERM, Montpellier, France.
  • De La Cruz E; Hospital de la Santa Creu i Sant Pau - Biomedical Research Institute Sant Pau - Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Kuhle J; Explorations neurologiques et centre SLA, Université Montpellier, CHU Gui de Chauliac, INM, INSERM, Montpellier, France.
  • Benkert P; Department of Neurology, University Hospital and University of Basel, Basel, Switzerland.
  • Mondesert E; Multiple Sclerosis Center and Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB), Departments of Biomedicine and Clinical Research, University Hospital and University of Basel, Basel, Switzerland.
  • Ginestet N; Department of Neurology, University Hospital and University of Basel, Basel, Switzerland.
  • Hirtz C; Multiple Sclerosis Center and Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB), Departments of Biomedicine and Clinical Research, University Hospital and University of Basel, Basel, Switzerland.
  • Camu W; LBPC-PPC, Université Montpellier, CHU Montpellier, INM INSERM, Montpellier, France.
  • Lehmann S; LBPC-PPC, Université Montpellier, CHU Montpellier, INM INSERM, Montpellier, France.
  • Esselin F; LBPC-PPC, Université Montpellier, CHU Montpellier, INM INSERM, Montpellier, France.
Eur J Neurol ; 30(7): 1919-1927, 2023 07.
Article em En | MEDLINE | ID: mdl-37029777
ABSTRACT

BACKGROUND:

The neurofilament light chain (NfL) assay is gradually becoming an essential diagnostic tool for the diagnosis of many neurological diseases including amyotrophic lateral sclerosis (ALS). Different methods for the determination of this biomarker in serum have been developed in recent years.

METHODS:

We measured blood NfL in 429 patients referred to the tertiary ALS center of Montpellier, France using two different ultrasensitive methods (Ella™ and Simoa™) and we compared the clinical performances of these two approaches. We also converted NfL values into age and body mass index-adjusted Z-scores to assess cut-off values of this biomarker in this clinical context.

RESULTS:

We show comparable diagnostic and prognostic performance of Ella™ and Simoa™ technologies in ALS, with specificities and sensitivities exceeding 80% for both. We propose cut-off values for serum NfL in this clinical context, thus enabling the routine clinical use of this biomarker.

CONCLUSION:

The use of NfL in routine clinical practice will help predict survival and improve diagnostic accuracy by distinguishing ALS from other neurological diseases and motor neuron disease mimics.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article