Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/45406
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dc.contributor.authorFRAUSSEN, Judith-
dc.contributor.authorIn't Veld, Sjors G. J. G.-
dc.contributor.authorvan Laake-Geelen, Charlotte C. M.-
dc.contributor.authorDepreitere, Bart-
dc.contributor.authorDeckers , Jens-
dc.contributor.authorPeuskens, Dieter-
dc.contributor.authorCornips, Erwin M. J.-
dc.contributor.authorBAMPS, Sven-
dc.contributor.authorTeunissen, Charlotte E.-
dc.contributor.authorSOMERS, Veerle-
dc.date.accessioned2025-02-25T12:24:58Z-
dc.date.available2025-02-25T12:24:58Z-
dc.date.issued2025-
dc.date.submitted2025-02-24T15:57:28Z-
dc.identifier.citationAnnals of neurology,-
dc.identifier.urihttp://hdl.handle.net/1942/45406-
dc.description.abstractObjectiveTraumatic spinal cord injury (SCI) is diagnosed by imaging and clinical scoring using the American Spinal Injury Association Impairment Scale (AIS). These methods have limited value for prognosis. Here, the prognostic value of plasma neurofilament-light (NfL), glial fibrillary acidic protein (GFAP), and contactin-1 (CNTN-1) was analyzed. MethodsBiomarker levels were determined in the plasma of traumatic SCI patients (n = 37) and healthy controls (n = 22). SCI samples (n = 112) were collected at different time points from 0 to 4 days to 18 weeks post-injury. NfL and GFAP were measured by single molecule array (Simoa) technology, CNTN-1 by Luminex. Baseline and outcome AIS and motor scores were collected as a measure of injury severity. ResultsNfL, GFAP, and CNTN-1 showed different kinetics in SCI patients over time. Baseline biomarker levels could identify AIS-A SCI patients (NfL + GFAP) and discriminate between patients with a motor score change <5 and those with a change >= 5 (NfL + GFAP+CNTN-1). Longitudinally, NfL could identify AIS-A patients up to 12 weeks post-SCI and discriminate between patients with a motor score change <5 and those with a change >= 5 up to 18 weeks post-SCI. Further, baseline biomarker levels positively (NfL + GFAP) or negatively (CNTN-1) correlated with outcome injury severity and together could accurately predict AIS conversion (AUC 0.863) and motor score change (AUC 0.857). This predictive ability was maintained in subacute/chronic SCI stages. InterpretationIn conclusion, plasma NfL, GFAP, and CNTN-1 are potential prognostic biomarkers in SCI. This is important for patient stratification in clinical trials, prediction of neurological outcome and informed decision-making in SCI treatment and rehabilitation. ANN NEUROL 2025-
dc.description.sponsorshipThe authors thank Kim Ulenaers (Hasselt University, Biomedical Research Institute, Belgium) for help with the sample and data collection, Prof. Tomas Menovsky (Antwerp University Hospital, Belgium) for patient inclusion, and dr. Liesbeth Bruckers and dr. Anna Ivanova (BioStat, Data Science Institute, Hasselt University, Belgium) for help with data analysis. This work was supported by Hasselt University and a grant from the Wings for Life Spinal Cord Research Foundation (WFL-BE-20/20).-
dc.language.isoen-
dc.publisherWILEY-
dc.rights2025 American Neurological Association-
dc.titleLongitudinal Plasma Biomarker Profiles Predict Neurological Outcome in Traumatic Spinal Cord Injury-
dc.typeJournal Contribution-
local.format.pages10-
local.bibliographicCitation.jcatA1-
dc.description.notesFraussen, J (corresponding author), UHasselt Hasselt Univ, Biomed Res Inst, Dept Immunol & Infect, Martelarenlaan 42, B-3500 Hasselt, Belgium.-
dc.description.notesjudith.fraussen@uhasselt.be-
local.publisher.place111 RIVER ST, HOBOKEN 07030-5774, NJ USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.statusEarly view-
dc.identifier.doi10.1002/ana.27198-
dc.identifier.isi001414715900001-
local.provider.typewosris-
local.description.affiliation[Fraussen, Judith; Somers, Veerle] UHasselt Hasselt Univ, Biomed Res Inst, Dept Immunol & Infect, Martelarenlaan 42, B-3500 Hasselt, Belgium.-
local.description.affiliation[In't Veld, Sjors G. J. G.; Teunissen, Charlotte E.] Vrije Univ, Amsterdam Univ Med Ctr, Dept Lab Med, Amsterdam Neurosci Neurodegenerat,Neurochem Lab, Amsterdam, Netherlands.-
local.description.affiliation[van Laake-Geelen, Charlotte C. M.] Adelante Ctr Expertise Rehabil & Audiol, Hoensbroek, Netherlands.-
local.description.affiliation[van Laake-Geelen, Charlotte C. M.] Maastricht Univ, Res Sch CAPHRI, Dept Rehabil Med, Maastricht, Netherlands.-
local.description.affiliation[Depreitere, Bart] Univ Hosp Leuven, Div Neurosurg, Leuven, Belgium.-
local.description.affiliation[Deckers, Jens] Algemeen Ziekenhuis AZ Turnhout, Dept Neurosurg, Turnhout, Belgium.-
local.description.affiliation[Deckers, Jens; Peuskens, Dieter; Cornips, Erwin M. J.] Ziekenhuis Oost Limburg, Dept Neurosurg, Genk, Belgium.-
local.description.affiliation[Bamps, Sven] Jessa Hosp, Dept Neurosurg, Hasselt, Belgium.-
local.uhasselt.internationalyes-
item.contributorFRAUSSEN, Judith-
item.contributorIn't Veld, Sjors G. J. G.-
item.contributorvan Laake-Geelen, Charlotte C. M.-
item.contributorDepreitere, Bart-
item.contributorDeckers , Jens-
item.contributorPeuskens, Dieter-
item.contributorCornips, Erwin M. J.-
item.contributorBAMPS, Sven-
item.contributorTeunissen, Charlotte E.-
item.contributorSOMERS, Veerle-
item.fullcitationFRAUSSEN, Judith; In't Veld, Sjors G. J. G.; van Laake-Geelen, Charlotte C. M.; Depreitere, Bart; Deckers , Jens; Peuskens, Dieter; Cornips, Erwin M. J.; BAMPS, Sven; Teunissen, Charlotte E. & SOMERS, Veerle (2025) Longitudinal Plasma Biomarker Profiles Predict Neurological Outcome in Traumatic Spinal Cord Injury. In: Annals of neurology,.-
item.embargoEndDate2025-07-05-
item.fulltextWith Fulltext-
item.accessRightsEmbargoed Access-
crisitem.journal.issn0364-5134-
crisitem.journal.eissn1531-8249-
Appears in Collections:Research publications
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