Cerebrospinal fluid kappa free light chains for the diagnosis of multiple sclerosis: A consensus statement.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
02 2023
Historique:
pubmed: 18 12 2022
medline: 15 2 2023
entrez: 17 12 2022
Statut: ppublish

Résumé

Cerebrospinal fluid (CSF) analysis is of utmost importance for diagnosis and differential diagnosis of patients with suspected multiple sclerosis (MS). Evidence of intrathecal immunoglobulin G (IgG) synthesis proves the inflammatory nature of the disease, increases diagnostic certainty and substitutes for dissemination in time according to current diagnostic criteria. The gold standard to determine intrathecal IgG synthesis is the detection of CSF-restricted oligoclonal bands (OCBs). However, advances in laboratory methods brought up κ-free light chains (FLCs) as a new biomarker, which are produced in excess over intact immunoglobulins and accumulate in CSF in the case of central nervous system-derived inflammation. Overwhelming evidence showed a high diagnostic accuracy of intrathecal κ-FLC synthesis in MS with sensitivity and specificity of approximately 90% similar to OCB. κ-FLCs have advantages as its detection is fast, easy, cost-effective, reliable, rater-independent and returning quantitative results which might also improve the value of predicting MS disease activity. An international panel of experts in MS and CSF diagnostics developed a consensus of all participants. Six recommendations are given for establishing standard CSF evaluation in patients suspected of having MS. The panel recommended to include intrathecal κ-FLC synthesis in the next revision of MS diagnostic criteria as an additional tool to measure intrathecal immunoglobulin synthesis.

Identifiants

pubmed: 36527368
doi: 10.1177/13524585221134217
pmc: PMC9925908
doi:

Substances chimiques

Immunoglobulin kappa-Chains 0
Immunoglobulin G 0
Biomarkers 0
Oligoclonal Bands 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

182-195

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Auteurs

Harald Hegen (H)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Georgina Arrambide (G)

Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.

Sharmilee Gnanapavan (S)

Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

Batia Kaplan (B)

Laboratory of Hematology, Sheba Medical Center, Ramat Gan, Israel.

Michael Khalil (M)

Department of Neurology, Medical University of Graz, Graz, Austria.

Ruba Saadeh (R)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA/Department of Neurology, Mayo Clinic, Rochester, MN, USA.

Charlotte Teunissen (C)

Neurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam Neuroscience, Program Neuroinflammation, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.

Hayrettin Tumani (H)

CSF Laboratory, Department of Neurology, University of Ulm, Ulm, Germany.

Luisa Maria Villar (LM)

Biostatistics Unit, Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Maria Alice V Willrich (MAV)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Henrik Zetterberg (H)

Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden/Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Gothenburg, Sweden/Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK/UK Dementia Research Institute at UCL, London, UK/Hong Kong Center for Neurodegenerative Diseases, Hong Kong, China.

Florian Deisenhammer (F)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

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