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ArticleNeurology(R) neuroimmunology & neuroinflammation2025

Diagnostic Utility of Kappa Free Light Chain Index in Adults With Inaugural Optic Neuritis.

Sarah Demortiere, Natacha Stolowy, Marine Perriguey, Clemence Boutiere, Audrey Rico, Frederic Hilezian, Blaise-Roger Ndjomo-Ndjomo, Pierre Durozard, Jan-Patrick Stellmann, Romain Marignier and 4 more

Abstract read
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Article in Neurology(R) neuroimmunology & neuroinflammation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Sarah DemortiereDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0002-8513-5443
Natacha StolowyDepartment of Ophtalmology, University Hospital of Marseille, France.ORCID 0000-0003-3662-3800
Marine PerrigueyDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0002-9470-0563
Clemence BoutiereDepartment of Neurology, University Hospital of Marseille, France.ORCID 0009-0001-3119-8203
Audrey RicoDepartment of Neurology, University Hospital of Marseille, France.ORCID 0009-0002-5395-9963
Frederic HilezianDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0002-5854-9325
Blaise-Roger Ndjomo-NdjomoCentre Hospitalier d'Ajaccio, France.
Pierre DurozardDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0003-3459-7741
Jan-Patrick StellmannCNRS, CRMBM, Aix Marseille Univ, France.ORCID 0000-0003-2565-2833
Romain MarignierService de Neurologie, sclérose en plaques, pathologies de la myéline et neuroinflammation, Hôpital Neurologique P. Wertheimer, Hospices Civils de Lyon, France.ORCID 0000-0002-5967-2800
José BoucrautUniversity Hospital of Marseille, Immunology Laboratory, France; and.
Jean PelletierDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0001-9730-7567
Adil MaaroufDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0002-6755-496X
Bertrand AudoinDepartment of Neurology, University Hospital of Marseille, France.ORCID 0000-0002-9860-7657

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesA simple, quick, and reproducible procedure for distinguishing multiple sclerosis (MS), myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), and neuromyelitis optica spectrum disorder (NMOSD) at inaugural optic neuritis (ION) could be highly valuable in guiding early management.

methodsWe included all adults admitted to the MS center of Marseille for ION between March 2016 and April 2024, with CSF analysis including the kappa free light chain (K-FLC) index. Receiver operating characteristic curves were used to measure the diagnostic ability of the K-FLC index.

resultsTwo hundred twenty-seven adults were admitted for ION; 210 (93%) had a K-FLC index measurement. MS was diagnosed in 84 (40%); clinically isolated syndrome suggestive of MS in 77 (36.5%), including 20 with future conversion to MS (CISwc); MOGAD in 26 (12.5%); NMOSD in 13 (6%); and other inflammatory disorders in 10 (5%). A K-FLC index ≥6.7 differentiated MS/CISwc from other diagnoses with specificity 86% and sensitivity 95% (area under the curve [AUC] 0.94). A K-FLC index <4.9 differentiated MOGAD from other diagnoses with specificity 63% and sensitivity 92% (AUC 0.78) and MOGAD from MS/CISwc with specificity 96% and sensitivity 92% (AUC 0.97). Among all patients, 93 (44%) had a K-FLC index <4.9: 24 of these (26%) had MOGAD and 5 (5.5%) MS/CISwc. Among the remaining patients with a K-FLC index ≥4.9 (n = 117), 2 (1.7%) had MOGAD (K-FLC index of 7.9 and 16.2) and 99 (85%) MS/CISwc. Among patients with normal MRI (n = 96), 73 (76%) had a K-FLC index <4.9: 22 of these (30%) had MOGAD, and none showed conversion to MS. Among the remaining patients with a K-FLC index ≥4.9 (n = 23), 2 (8.5%) had MOGAD and 7 (30.5%) showed conversion to MS. The K-FLC index did not differentiate NMOSD from other diagnoses and only moderately differentiated NMO from MS/CISwc (AUC 0.80). DISCUSSION: The K-FLC index is an accessible biomarker to guide early diagnosis in patients with ION. The probability of MOGAD in patients with ION and a K-FLC index ≥4.9 is low even in case of normal brain/spinal cord MRI. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that for patients with ION, the K-FLC index can distinguish between MS/CISwc and MOGAD.

Indexed as

Immunoglobulin kappa-ChainsMultiple SclerosisNeuromyelitis OpticaOptic NeuritisAdultAgedBiomarkersDiagnosis, DifferentialFemaleHumansMaleMiddle AgedMyelin-Oligodendrocyte GlycoproteinYoung AdultBiomarkersImmunoglobulin kappa-ChainsMyelin-Oligodendrocyte Glycoprotein

Identifiers

PMID40085804
PMCPMC11913550

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.