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Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy
OBJECTIVE: To test the hypothesis that the intrathecal synthesis of free light chain kappa (FLC-k) can be used as a CSF biomarker to differentiate patients with myelitis due to multiple sclerosis (MS), myelitis due to neuromyelitis optica spectrum disease (NMOSD), and noninflammatory myelopathy, we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524577/ https://www.ncbi.nlm.nih.gov/pubmed/32948648 http://dx.doi.org/10.1212/NXI.0000000000000892 |
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author | Süße, Marie Feistner, Fritz Grothe, Matthias Nauck, Matthias Dressel, Alexander Hannich, Malte Johannes |
author_facet | Süße, Marie Feistner, Fritz Grothe, Matthias Nauck, Matthias Dressel, Alexander Hannich, Malte Johannes |
author_sort | Süße, Marie |
collection | PubMed |
description | OBJECTIVE: To test the hypothesis that the intrathecal synthesis of free light chain kappa (FLC-k) can be used as a CSF biomarker to differentiate patients with myelitis due to multiple sclerosis (MS), myelitis due to neuromyelitis optica spectrum disease (NMOSD), and noninflammatory myelopathy, we analyzed FLC-k in 26 patients with MS myelitis, 9 patients with NMOSD myelitis, and 14 patients with myelopathy. METHODS: This is a retrospective monocentric cohort study. FLC-k were analyzed using the nephelometric Siemens FLC-k kit in paired samples of CSF and sera. Intrathecal fraction (IF) of FLC-k was plotted in a FLC-k quotient diagram. RESULTS: Ninety-six percent of patients with MS myelitis had an intrathecal synthesis of FLC-k in comparison with 55.6% for NMOSD and 14.3% of patients with noninflammatory myelopathy. The locally synthesized absolute amount of FLC-k was significantly higher in patients with myelitis due to MS than in patients with NMOSD (p = 0.038) or noninflammatory myelopathy (p < 0.0001). The sensitivity of FLC-k synthesis to detect inflammation in patients with myelitis is 85.7%. Using a receiver operating characteristic analysis, FLC-k IF >78% can discriminate patients with myelitis due to MS and NMOSD with a sensitivity of 88.5% and a specificity of 88.9% CONCLUSIONS: With the hyperbolic reference range in quotient diagrams for FLC-k, it is possible to distinguish inflammatory myelitis from noninflammatory myelopathies. An FLC-k IF >78% can be a hint to suspect myelitis due to MS rather than NMOSD. |
format | Online Article Text |
id | pubmed-7524577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-75245772020-10-14 Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy Süße, Marie Feistner, Fritz Grothe, Matthias Nauck, Matthias Dressel, Alexander Hannich, Malte Johannes Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To test the hypothesis that the intrathecal synthesis of free light chain kappa (FLC-k) can be used as a CSF biomarker to differentiate patients with myelitis due to multiple sclerosis (MS), myelitis due to neuromyelitis optica spectrum disease (NMOSD), and noninflammatory myelopathy, we analyzed FLC-k in 26 patients with MS myelitis, 9 patients with NMOSD myelitis, and 14 patients with myelopathy. METHODS: This is a retrospective monocentric cohort study. FLC-k were analyzed using the nephelometric Siemens FLC-k kit in paired samples of CSF and sera. Intrathecal fraction (IF) of FLC-k was plotted in a FLC-k quotient diagram. RESULTS: Ninety-six percent of patients with MS myelitis had an intrathecal synthesis of FLC-k in comparison with 55.6% for NMOSD and 14.3% of patients with noninflammatory myelopathy. The locally synthesized absolute amount of FLC-k was significantly higher in patients with myelitis due to MS than in patients with NMOSD (p = 0.038) or noninflammatory myelopathy (p < 0.0001). The sensitivity of FLC-k synthesis to detect inflammation in patients with myelitis is 85.7%. Using a receiver operating characteristic analysis, FLC-k IF >78% can discriminate patients with myelitis due to MS and NMOSD with a sensitivity of 88.5% and a specificity of 88.9% CONCLUSIONS: With the hyperbolic reference range in quotient diagrams for FLC-k, it is possible to distinguish inflammatory myelitis from noninflammatory myelopathies. An FLC-k IF >78% can be a hint to suspect myelitis due to MS rather than NMOSD. Lippincott Williams & Wilkins 2020-09-18 /pmc/articles/PMC7524577/ /pubmed/32948648 http://dx.doi.org/10.1212/NXI.0000000000000892 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Süße, Marie Feistner, Fritz Grothe, Matthias Nauck, Matthias Dressel, Alexander Hannich, Malte Johannes Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
title | Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
title_full | Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
title_fullStr | Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
title_full_unstemmed | Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
title_short | Free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
title_sort | free light chains kappa can differentiate between myelitis and noninflammatory myelopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524577/ https://www.ncbi.nlm.nih.gov/pubmed/32948648 http://dx.doi.org/10.1212/NXI.0000000000000892 |
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