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Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus

OBJECTIVE: We explored the potential of neurofilament light chain (NfL) in serum and cerebrospinal fluid as a biomarker for neurodestruction in status epilepticus. METHODS: In a retrospective analysis, we measured NfL in serum and cerebrospinal fluid samples of patients with status epilepticus using...

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Autores principales: Margraf, Nils G., Dargvainiene, Justina, Theel, Emily, Leypoldt, Frank, Lieb, Wolfgang, Franke, Andre, Berger, Klaus, Kuhle, Jens, Kuhlenbaeumer, Gregor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025237/
https://www.ncbi.nlm.nih.gov/pubmed/36624182
http://dx.doi.org/10.1007/s00415-022-11547-4
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author Margraf, Nils G.
Dargvainiene, Justina
Theel, Emily
Leypoldt, Frank
Lieb, Wolfgang
Franke, Andre
Berger, Klaus
Kuhle, Jens
Kuhlenbaeumer, Gregor
author_facet Margraf, Nils G.
Dargvainiene, Justina
Theel, Emily
Leypoldt, Frank
Lieb, Wolfgang
Franke, Andre
Berger, Klaus
Kuhle, Jens
Kuhlenbaeumer, Gregor
author_sort Margraf, Nils G.
collection PubMed
description OBJECTIVE: We explored the potential of neurofilament light chain (NfL) in serum and cerebrospinal fluid as a biomarker for neurodestruction in status epilepticus. METHODS: In a retrospective analysis, we measured NfL in serum and cerebrospinal fluid samples of patients with status epilepticus using a highly sensitive single-molecule array technique (Simoa). Status epilepticus was diagnosed according to ILAE criteria. Additionally, we employed an alternative classification with more emphasis on the course of status epilepticus. We used data from three large control groups to compare NfL in status epilepticus versus neurologically healthy controls. RESULTS: We included 28 patients (mean age: 69.4 years, SD: 15 years) with a median status duration of 44 h (IQR: 80 h). Twenty-one patients (75%) suffered from convulsive status epilepticus and seven (25%) from non-convulsive status epilepticus. Six patients died (21%). Cerebrospinal fluid and serum NfL concentrations showed a high correlation (r = 0.73, p < 0.001, Pearson). The main determinant of NfL concentration was the status duration. NfL concentrations did not differ between convulsive status epilepticus and convulsive status epilepticus classified according to the ILAE or to the alternative classification without and with adjusting for status duration and time between status onset and sampling. We found no association of NfL concentration with death, treatment refractoriness, or prognostic scores. CONCLUSION: The results suggest that neurodestruction in status epilepticus measured by NfL is mainly determined by status duration, not status type nor therapy refractoriness. Therefore, our results suggest that regarding neurodestruction convulsive and non-convulsive status epilepticus are both neurological emergencies of comparable urgency. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-022-11547-4.
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spelling pubmed-100252372023-03-21 Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus Margraf, Nils G. Dargvainiene, Justina Theel, Emily Leypoldt, Frank Lieb, Wolfgang Franke, Andre Berger, Klaus Kuhle, Jens Kuhlenbaeumer, Gregor J Neurol Original Communication OBJECTIVE: We explored the potential of neurofilament light chain (NfL) in serum and cerebrospinal fluid as a biomarker for neurodestruction in status epilepticus. METHODS: In a retrospective analysis, we measured NfL in serum and cerebrospinal fluid samples of patients with status epilepticus using a highly sensitive single-molecule array technique (Simoa). Status epilepticus was diagnosed according to ILAE criteria. Additionally, we employed an alternative classification with more emphasis on the course of status epilepticus. We used data from three large control groups to compare NfL in status epilepticus versus neurologically healthy controls. RESULTS: We included 28 patients (mean age: 69.4 years, SD: 15 years) with a median status duration of 44 h (IQR: 80 h). Twenty-one patients (75%) suffered from convulsive status epilepticus and seven (25%) from non-convulsive status epilepticus. Six patients died (21%). Cerebrospinal fluid and serum NfL concentrations showed a high correlation (r = 0.73, p < 0.001, Pearson). The main determinant of NfL concentration was the status duration. NfL concentrations did not differ between convulsive status epilepticus and convulsive status epilepticus classified according to the ILAE or to the alternative classification without and with adjusting for status duration and time between status onset and sampling. We found no association of NfL concentration with death, treatment refractoriness, or prognostic scores. CONCLUSION: The results suggest that neurodestruction in status epilepticus measured by NfL is mainly determined by status duration, not status type nor therapy refractoriness. Therefore, our results suggest that regarding neurodestruction convulsive and non-convulsive status epilepticus are both neurological emergencies of comparable urgency. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-022-11547-4. Springer Berlin Heidelberg 2023-01-09 2023 /pmc/articles/PMC10025237/ /pubmed/36624182 http://dx.doi.org/10.1007/s00415-022-11547-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Communication
Margraf, Nils G.
Dargvainiene, Justina
Theel, Emily
Leypoldt, Frank
Lieb, Wolfgang
Franke, Andre
Berger, Klaus
Kuhle, Jens
Kuhlenbaeumer, Gregor
Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus
title Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus
title_full Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus
title_fullStr Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus
title_full_unstemmed Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus
title_short Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus
title_sort neurofilament light (nfl) as biomarker in serum and csf in status epilepticus
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025237/
https://www.ncbi.nlm.nih.gov/pubmed/36624182
http://dx.doi.org/10.1007/s00415-022-11547-4
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