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Enhancing the clinical value of serum neurofilament light chain measurement

BACKGROUND: Serum neurofilament light chain (sNFL) is becoming an important biomarker of neuro-axonal injury. Though sNFL correlates with CSF NFL (cNFL), 40% to 60% of variance remains unexplained. We aimed to mathematically adjust sNFL to strengthen its clinical value. METHODS: We measured NFL in a...

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Autores principales: Kosa, Peter, Masvekar, Ruturaj, Komori, Mika, Phillips, Jonathan, Ramesh, Vighnesh, Varosanec, Mihael, Sandford, Mary, Bielekova, Bibiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462467/
https://www.ncbi.nlm.nih.gov/pubmed/35737460
http://dx.doi.org/10.1172/jci.insight.161415
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author Kosa, Peter
Masvekar, Ruturaj
Komori, Mika
Phillips, Jonathan
Ramesh, Vighnesh
Varosanec, Mihael
Sandford, Mary
Bielekova, Bibiana
author_facet Kosa, Peter
Masvekar, Ruturaj
Komori, Mika
Phillips, Jonathan
Ramesh, Vighnesh
Varosanec, Mihael
Sandford, Mary
Bielekova, Bibiana
author_sort Kosa, Peter
collection PubMed
description BACKGROUND: Serum neurofilament light chain (sNFL) is becoming an important biomarker of neuro-axonal injury. Though sNFL correlates with CSF NFL (cNFL), 40% to 60% of variance remains unexplained. We aimed to mathematically adjust sNFL to strengthen its clinical value. METHODS: We measured NFL in a blinded fashion in 1138 matched CSF and serum samples from 571 patients. Multiple linear regression (MLR) models constructed in the training cohort were validated in an independent cohort. RESULTS: An MLR model that included age, blood urea nitrogen, alkaline phosphatase, creatinine, and weight improved correlations of cNFL with sNFL (from R(2) = 0.57 to 0.67). Covariate adjustment significantly improved the correlation of sNFL with the number of contrast-enhancing lesions (from R(2) = 0.18 to 0.28; 36% improvement) in the validation cohort of patients with multiple sclerosis (MS). Unexpectedly, only sNFL, but not cNFL, weakly but significantly correlated with cross-sectional MS severity outcomes. Investigating 2 nonoverlapping hypotheses, we showed that patients with proportionally higher sNFL to cNFL had higher clinical and radiological evidence of spinal cord (SC) injury and probably released NFL from peripheral axons into blood, bypassing the CSF. CONCLUSION: sNFL captures 2 sources of axonal injury, central and peripheral, the latter reflecting SC damage, which primarily drives disability progression in MS. TRIAL REGISTRATION: ClinicalTrials.gov NCT00794352. FUNDING: Division of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH (AI001242 and AI001243).
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spelling pubmed-94624672022-09-13 Enhancing the clinical value of serum neurofilament light chain measurement Kosa, Peter Masvekar, Ruturaj Komori, Mika Phillips, Jonathan Ramesh, Vighnesh Varosanec, Mihael Sandford, Mary Bielekova, Bibiana JCI Insight Clinical Medicine BACKGROUND: Serum neurofilament light chain (sNFL) is becoming an important biomarker of neuro-axonal injury. Though sNFL correlates with CSF NFL (cNFL), 40% to 60% of variance remains unexplained. We aimed to mathematically adjust sNFL to strengthen its clinical value. METHODS: We measured NFL in a blinded fashion in 1138 matched CSF and serum samples from 571 patients. Multiple linear regression (MLR) models constructed in the training cohort were validated in an independent cohort. RESULTS: An MLR model that included age, blood urea nitrogen, alkaline phosphatase, creatinine, and weight improved correlations of cNFL with sNFL (from R(2) = 0.57 to 0.67). Covariate adjustment significantly improved the correlation of sNFL with the number of contrast-enhancing lesions (from R(2) = 0.18 to 0.28; 36% improvement) in the validation cohort of patients with multiple sclerosis (MS). Unexpectedly, only sNFL, but not cNFL, weakly but significantly correlated with cross-sectional MS severity outcomes. Investigating 2 nonoverlapping hypotheses, we showed that patients with proportionally higher sNFL to cNFL had higher clinical and radiological evidence of spinal cord (SC) injury and probably released NFL from peripheral axons into blood, bypassing the CSF. CONCLUSION: sNFL captures 2 sources of axonal injury, central and peripheral, the latter reflecting SC damage, which primarily drives disability progression in MS. TRIAL REGISTRATION: ClinicalTrials.gov NCT00794352. FUNDING: Division of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH (AI001242 and AI001243). American Society for Clinical Investigation 2022-08-08 /pmc/articles/PMC9462467/ /pubmed/35737460 http://dx.doi.org/10.1172/jci.insight.161415 Text en © 2022, Kosa et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Medicine
Kosa, Peter
Masvekar, Ruturaj
Komori, Mika
Phillips, Jonathan
Ramesh, Vighnesh
Varosanec, Mihael
Sandford, Mary
Bielekova, Bibiana
Enhancing the clinical value of serum neurofilament light chain measurement
title Enhancing the clinical value of serum neurofilament light chain measurement
title_full Enhancing the clinical value of serum neurofilament light chain measurement
title_fullStr Enhancing the clinical value of serum neurofilament light chain measurement
title_full_unstemmed Enhancing the clinical value of serum neurofilament light chain measurement
title_short Enhancing the clinical value of serum neurofilament light chain measurement
title_sort enhancing the clinical value of serum neurofilament light chain measurement
topic Clinical Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462467/
https://www.ncbi.nlm.nih.gov/pubmed/35737460
http://dx.doi.org/10.1172/jci.insight.161415
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