Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis

Background and Objectives Selecting the most appropriate blood tests is crucial for the management of patients with amyotrophic lateral sclerosis (ALS). This study evaluates the diagnostic and prognostic performance of neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and phos...

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Autores: Mondesert, E., Delaby, Constance|||0000-0002-8606-6814, De La Cruz, E.|||0000-0003-3345-1628, Kuhle, Jens|||0000-0002-6963-8892, Benkert, P.|||0000-0001-6525-8174, Pradeilles, N., Duchiron, M., Morchikh, M., Camu, W., Cristol, J.P., Hirtz, C., Esselin, F., Lehmann, Sylvain|||0000-0001-6117-562X
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:321758
Acceso en línea:https://ddd.uab.cat/record/321758
https://dx.doi.org/urn:doi:10.1212/WNL.0000000000213400
Access Level:acceso abierto
Palabra clave:Aged
Amyotrophic Lateral Sclerosis
Biomarkers
Cohort Studies
Female
Glial Fibrillary Acidic Protein
Humans
Male
Middle Aged
Neurofilament Proteins
Phosphorylation
Prognosis
Tau Proteins
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spelling Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral SclerosisMondesert, E.Delaby, Constance|||0000-0002-8606-6814De La Cruz, E.|||0000-0003-3345-1628Kuhle, Jens|||0000-0002-6963-8892Benkert, P.|||0000-0001-6525-8174Pradeilles, N.Duchiron, M.Morchikh, M.Camu, W.Cristol, J.P.Hirtz, C.Esselin, F.Lehmann, Sylvain|||0000-0001-6117-562XAgedAmyotrophic Lateral SclerosisBiomarkersCohort StudiesFemaleGlial Fibrillary Acidic ProteinHumansMaleMiddle AgedNeurofilament ProteinsPhosphorylationPrognosisTau ProteinsBackground and Objectives Selecting the most appropriate blood tests is crucial for the management of patients with amyotrophic lateral sclerosis (ALS). This study evaluates the diagnostic and prognostic performance of neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and phosphorylated tau 181 (pTau181) biomarkers in ALS to establish their clinical relevance and cutoff values. Methods In a cohort of patients from the ALS center in Montpellier, we conducted a head-to-head comparison of 4 different technologies and 3 distinct serum analytes: NfL was tested using the ultrasensitive Simoa and the microfluidic Ella platforms, along with 2 assays recently set up on clinical-grade platforms: Lumipulse and Elecsys. We also used Elecsys to assess serum GFAP and pTau181. Results Our cohort included 139 patients with ALS and 70 non-ALS patients, with a mean age of 66.1 ± 11.4 years and 47.4% of women. The mean follow-up was 42 ± 26.3 months for patients with ALS and 141.6 ± 106.3 months for non-ALS patients, with a mortality rate of 85.5% vs 7.7%. There was a high correlation between all methods tested for serum NfL quantification (R = 0.939 to 0.963). The area under the curve (AUC) for ALS diagnosis was 0.889 (0.827-0.932) for NfL Simoa, 0.906 (0.847-0.944) for Ella, 0.912 (0.853-0.948) for Lumipulse, and 0.910 (0.851-0.946) for Elecsys. Serum pTau181 and GFAP showed poor diagnostic performance with AUCs of 0.565 (0.472-0.649) and 0.546 (0.461-0.636), respectively. Kaplan-Meier survival analysis revealed significant hazard ratios (4.4-5.4) for blood NfL. Patients with ALS had a 40%-50% chance of surviving 50 weeks below the prognostic cutoff values while survival rates dropped to near zero above. NfL and GFAP levels were associated with age and body mass index, considered confounding factors. pTau181 levels varied significantly in patients with ALS depending on the site of onset. Discussion This study demonstrates the consistent performance of 4 immunoassays for serum NfL quantification in ALS. NfL showed high diagnostic and prognostic accuracy, making it suitable for individual assessment, unlike GFAP or pTau181. We propose diagnostic and prognostic cutoff values for serum NfL, providing a basis for wider implementation, especially with the clinically accredited Lumipulse and Elecsys platforms, which are becoming standard practice.Universitat Autònoma de Barcelona 22025-01-0120252025-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/321758https://dx.doi.org/urn:doi:10.1212/WNL.0000000000213400reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:3217582026-06-06T12:50:31Z
dc.title.none.fl_str_mv Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
title Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
spellingShingle Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
Mondesert, E.
Aged
Amyotrophic Lateral Sclerosis
Biomarkers
Cohort Studies
Female
Glial Fibrillary Acidic Protein
Humans
Male
Middle Aged
Neurofilament Proteins
Phosphorylation
Prognosis
Tau Proteins
title_short Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
title_full Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
title_fullStr Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
title_full_unstemmed Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
title_sort Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis
dc.creator.none.fl_str_mv Mondesert, E.
Delaby, Constance|||0000-0002-8606-6814
De La Cruz, E.|||0000-0003-3345-1628
Kuhle, Jens|||0000-0002-6963-8892
Benkert, P.|||0000-0001-6525-8174
Pradeilles, N.
Duchiron, M.
Morchikh, M.
Camu, W.
Cristol, J.P.
Hirtz, C.
Esselin, F.
Lehmann, Sylvain|||0000-0001-6117-562X
author Mondesert, E.
author_facet Mondesert, E.
Delaby, Constance|||0000-0002-8606-6814
De La Cruz, E.|||0000-0003-3345-1628
Kuhle, Jens|||0000-0002-6963-8892
Benkert, P.|||0000-0001-6525-8174
Pradeilles, N.
Duchiron, M.
Morchikh, M.
Camu, W.
Cristol, J.P.
Hirtz, C.
Esselin, F.
Lehmann, Sylvain|||0000-0001-6117-562X
author_role author
author2 Delaby, Constance|||0000-0002-8606-6814
De La Cruz, E.|||0000-0003-3345-1628
Kuhle, Jens|||0000-0002-6963-8892
Benkert, P.|||0000-0001-6525-8174
Pradeilles, N.
Duchiron, M.
Morchikh, M.
Camu, W.
Cristol, J.P.
Hirtz, C.
Esselin, F.
Lehmann, Sylvain|||0000-0001-6117-562X
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universitat Autònoma de Barcelona
dc.subject.none.fl_str_mv Aged
Amyotrophic Lateral Sclerosis
Biomarkers
Cohort Studies
Female
Glial Fibrillary Acidic Protein
Humans
Male
Middle Aged
Neurofilament Proteins
Phosphorylation
Prognosis
Tau Proteins
topic Aged
Amyotrophic Lateral Sclerosis
Biomarkers
Cohort Studies
Female
Glial Fibrillary Acidic Protein
Humans
Male
Middle Aged
Neurofilament Proteins
Phosphorylation
Prognosis
Tau Proteins
description Background and Objectives Selecting the most appropriate blood tests is crucial for the management of patients with amyotrophic lateral sclerosis (ALS). This study evaluates the diagnostic and prognostic performance of neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and phosphorylated tau 181 (pTau181) biomarkers in ALS to establish their clinical relevance and cutoff values. Methods In a cohort of patients from the ALS center in Montpellier, we conducted a head-to-head comparison of 4 different technologies and 3 distinct serum analytes: NfL was tested using the ultrasensitive Simoa and the microfluidic Ella platforms, along with 2 assays recently set up on clinical-grade platforms: Lumipulse and Elecsys. We also used Elecsys to assess serum GFAP and pTau181. Results Our cohort included 139 patients with ALS and 70 non-ALS patients, with a mean age of 66.1 ± 11.4 years and 47.4% of women. The mean follow-up was 42 ± 26.3 months for patients with ALS and 141.6 ± 106.3 months for non-ALS patients, with a mortality rate of 85.5% vs 7.7%. There was a high correlation between all methods tested for serum NfL quantification (R = 0.939 to 0.963). The area under the curve (AUC) for ALS diagnosis was 0.889 (0.827-0.932) for NfL Simoa, 0.906 (0.847-0.944) for Ella, 0.912 (0.853-0.948) for Lumipulse, and 0.910 (0.851-0.946) for Elecsys. Serum pTau181 and GFAP showed poor diagnostic performance with AUCs of 0.565 (0.472-0.649) and 0.546 (0.461-0.636), respectively. Kaplan-Meier survival analysis revealed significant hazard ratios (4.4-5.4) for blood NfL. Patients with ALS had a 40%-50% chance of surviving 50 weeks below the prognostic cutoff values while survival rates dropped to near zero above. NfL and GFAP levels were associated with age and body mass index, considered confounding factors. pTau181 levels varied significantly in patients with ALS depending on the site of onset. Discussion This study demonstrates the consistent performance of 4 immunoassays for serum NfL quantification in ALS. NfL showed high diagnostic and prognostic accuracy, making it suitable for individual assessment, unlike GFAP or pTau181. We propose diagnostic and prognostic cutoff values for serum NfL, providing a basis for wider implementation, especially with the clinically accredited Lumipulse and Elecsys platforms, which are becoming standard practice.
publishDate 2025
dc.date.none.fl_str_mv 2
2025-01-01
2025
2025-01-01
dc.type.none.fl_str_mv Article
http://purl.org/coar/resource_type/c_6501
VoR
http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://ddd.uab.cat/record/321758
https://dx.doi.org/urn:doi:10.1212/WNL.0000000000213400
url https://ddd.uab.cat/record/321758
https://dx.doi.org/urn:doi:10.1212/WNL.0000000000213400
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Dipòsit Digital de Documents de la UAB
instname:Universitat Autònoma de Barcelona
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