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Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome
BACKGROUND: Guillain-Barré syndrome (GBS) is an autoimmune disease that results in demyelination and axonal damage. Five percent of patients die and 20% remain significantly disabled on recovery. Recovery is slow in most cases and eventual disability is difficult to predict, especially early in the...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079539/ https://www.ncbi.nlm.nih.gov/pubmed/32183837 http://dx.doi.org/10.1186/s12974-020-01737-0 |
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author | Altmann, Patrick De Simoni, Desiree Kaider, Alexandra Ludwig, Birgit Rath, Jakob Leutmezer, Fritz Zimprich, Fritz Hoeftberger, Romana Lunn, Michael P. Heslegrave, Amanda Berger, Thomas Zetterberg, Henrik Rommer, Paulus Stefan |
author_facet | Altmann, Patrick De Simoni, Desiree Kaider, Alexandra Ludwig, Birgit Rath, Jakob Leutmezer, Fritz Zimprich, Fritz Hoeftberger, Romana Lunn, Michael P. Heslegrave, Amanda Berger, Thomas Zetterberg, Henrik Rommer, Paulus Stefan |
author_sort | Altmann, Patrick |
collection | PubMed |
description | BACKGROUND: Guillain-Barré syndrome (GBS) is an autoimmune disease that results in demyelination and axonal damage. Five percent of patients die and 20% remain significantly disabled on recovery. Recovery is slow in most cases and eventual disability is difficult to predict, especially early in the disease. Blood or cerebrospinal fluid (CSF) biomarkers that could help identify patients at risk of poor outcome are required. We measured serum neurofilament light chain (sNfL) concentrations from blood taken upon admission and investigated a correlation between sNfL and clinical outcome. METHODS: Baseline sNfL levels in 27 GBS patients were compared with a control group of 22 patients with diagnoses not suggestive of any axonal damage. Clinical outcome parameters for GBS patients included (i) the Hughes Functional Score (HFS) at admission, nadir, and discharge; (ii) the number of days hospitalised; and (iii) whether intensive care was necessary. RESULTS: The median sNfL concentration in our GBS sample on admission was 85.5 pg/ml versus 9.1 pg/ml in controls. A twofold increase in sNfL concentration at baseline was associated with an HFS increase of 0.6 at nadir and reduced the likelihood of discharge with favourable outcome by a factor of almost three. Higher sNfL levels upon admission correlated well with hospitalisation time (r(s) = 0.69, p < 0.0001), during which transfer to intensive care occurred more frequently at an odds ratio of 2.4. Patients with baseline sNfL levels below 85.5 pg/ml had a 93% chance of being discharged with an unimpaired walking ability. CONCLUSIONS: sNfL levels measured at hospital admission correlated with clinical outcome in GBS patients. These results represent amounts of acute axonal damage and reflect mechanisms resulting in disability in GBS. Thus, sNfL may serve as a convenient blood-borne biomarker to personalise patient care by identifying those at higher risk of poor outcome. |
format | Online Article Text |
id | pubmed-7079539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70795392020-03-23 Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome Altmann, Patrick De Simoni, Desiree Kaider, Alexandra Ludwig, Birgit Rath, Jakob Leutmezer, Fritz Zimprich, Fritz Hoeftberger, Romana Lunn, Michael P. Heslegrave, Amanda Berger, Thomas Zetterberg, Henrik Rommer, Paulus Stefan J Neuroinflammation Research BACKGROUND: Guillain-Barré syndrome (GBS) is an autoimmune disease that results in demyelination and axonal damage. Five percent of patients die and 20% remain significantly disabled on recovery. Recovery is slow in most cases and eventual disability is difficult to predict, especially early in the disease. Blood or cerebrospinal fluid (CSF) biomarkers that could help identify patients at risk of poor outcome are required. We measured serum neurofilament light chain (sNfL) concentrations from blood taken upon admission and investigated a correlation between sNfL and clinical outcome. METHODS: Baseline sNfL levels in 27 GBS patients were compared with a control group of 22 patients with diagnoses not suggestive of any axonal damage. Clinical outcome parameters for GBS patients included (i) the Hughes Functional Score (HFS) at admission, nadir, and discharge; (ii) the number of days hospitalised; and (iii) whether intensive care was necessary. RESULTS: The median sNfL concentration in our GBS sample on admission was 85.5 pg/ml versus 9.1 pg/ml in controls. A twofold increase in sNfL concentration at baseline was associated with an HFS increase of 0.6 at nadir and reduced the likelihood of discharge with favourable outcome by a factor of almost three. Higher sNfL levels upon admission correlated well with hospitalisation time (r(s) = 0.69, p < 0.0001), during which transfer to intensive care occurred more frequently at an odds ratio of 2.4. Patients with baseline sNfL levels below 85.5 pg/ml had a 93% chance of being discharged with an unimpaired walking ability. CONCLUSIONS: sNfL levels measured at hospital admission correlated with clinical outcome in GBS patients. These results represent amounts of acute axonal damage and reflect mechanisms resulting in disability in GBS. Thus, sNfL may serve as a convenient blood-borne biomarker to personalise patient care by identifying those at higher risk of poor outcome. BioMed Central 2020-03-17 /pmc/articles/PMC7079539/ /pubmed/32183837 http://dx.doi.org/10.1186/s12974-020-01737-0 Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Altmann, Patrick De Simoni, Desiree Kaider, Alexandra Ludwig, Birgit Rath, Jakob Leutmezer, Fritz Zimprich, Fritz Hoeftberger, Romana Lunn, Michael P. Heslegrave, Amanda Berger, Thomas Zetterberg, Henrik Rommer, Paulus Stefan Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome |
title | Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome |
title_full | Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome |
title_fullStr | Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome |
title_full_unstemmed | Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome |
title_short | Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome |
title_sort | increased serum neurofilament light chain concentration indicates poor outcome in guillain-barré syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079539/ https://www.ncbi.nlm.nih.gov/pubmed/32183837 http://dx.doi.org/10.1186/s12974-020-01737-0 |
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