Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis

Aim. The aim of this study was to identify whether NfL and CXCL13 cerebrospinal fluid (CSF) concentrations at diagnostic lumbar puncture can predict the course of multiple sclerosis (MS) in terms of relapses, higher expanded disability status scale (EDSS) and magnetic resonance imaging (MRI) activit...

Full description

Bibliographic Details
Main Authors: Pavel Hradilek, Kamila Zondra Revendova, Jana Horakova, Radovan Bunganic, Ondrej Pelisek, David Zeman, Pavla Hanzlikova, Pavlina Kusnierova
Format: Article
Language:English
Published: Palacký University Olomouc, Faculty of Medicine and Dentistry 2023-03-01
Series:Biomedical Papers
Subjects:
Online Access:https://biomed.papers.upol.cz/artkey/bio-202301-0005_cerebrospinal-fluid-neurofilament-light-chains-and-cxcl13-as-predictive-factors-for-clinical-course-of-multiple.php
_version_ 1797835560767717376
author Pavel Hradilek
Kamila Zondra Revendova
Jana Horakova
Radovan Bunganic
Ondrej Pelisek
David Zeman
Pavla Hanzlikova
Pavlina Kusnierova
author_facet Pavel Hradilek
Kamila Zondra Revendova
Jana Horakova
Radovan Bunganic
Ondrej Pelisek
David Zeman
Pavla Hanzlikova
Pavlina Kusnierova
author_sort Pavel Hradilek
collection DOAJ
description Aim. The aim of this study was to identify whether NfL and CXCL13 cerebrospinal fluid (CSF) concentrations at diagnostic lumbar puncture can predict the course of multiple sclerosis (MS) in terms of relapses, higher expanded disability status scale (EDSS) and magnetic resonance imaging (MRI) activity. Methods. We conducted a single-centre prospective observational cohort study at the MS center, University Hospital Ostrava, Czech Republic. CSF NfL (cNfL) and CXCL13 concentrations were examined (ELISA method) in patients with clinically isolated syndrome (CIS) and relapsing-remitting MS (RRMS) at the time of diagnostic lumbar puncture. Results. A total of 44 patients with CIS or early RRMS were enrolled, 31 (70.5%) of whom were women. The median age at the time of CSF sampling was 31.21 years (IQR 25.43-39.32), and the follow-up period was 54.6 months (IQR 44.03-59.48). In the simple and multiple logistic regression models, CXCL13 levels did not predict relapses, MRI activity or EDSS > 2.5. Similarly, cNfL concentrations did not predict relapses or MRI activity in either model. In the multiple regression, higher cNfL levels were associated with reaching EDSS > 2.5 (odds ratio [OR] 1.002, 95% confidence interval [CI] 1.000 to 1.003). Conclusions. Our data did not confirm cNfL and/or CXCL13 CSF levels were predictive factors for disease activity such as relapses and MRI activity at the time of diagnostic lumbar puncture in patients with RRMS. While cNfL CSF levels predicted higher disability only after adjustment for other known risk factors, elevated CSF CXCL13 did not predict higher disability at all.
first_indexed 2024-04-09T14:54:32Z
format Article
id doaj.art-ad186c4a3e0d4e1f8ea520ddeff4aab0
institution Directory Open Access Journal
issn 1213-8118
1804-7521
language English
last_indexed 2024-04-09T14:54:32Z
publishDate 2023-03-01
publisher Palacký University Olomouc, Faculty of Medicine and Dentistry
record_format Article
series Biomedical Papers
spelling doaj.art-ad186c4a3e0d4e1f8ea520ddeff4aab02023-05-02T08:04:03ZengPalacký University Olomouc, Faculty of Medicine and DentistryBiomedical Papers1213-81181804-75212023-03-011671303510.5507/bp.2023.002bio-202301-0005Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosisPavel Hradilek0Kamila Zondra Revendova1Jana Horakova2Radovan Bunganic3Ondrej Pelisek4David Zeman5Pavla Hanzlikova6Pavlina Kusnierova7Department of Clinical Neurosciences, Faculty of Medicine, University of Ostrava, Ostrava, Czech RepublicDepartment of Clinical Neurosciences, Faculty of Medicine, University of Ostrava, Ostrava, Czech RepublicDepartment of Neurology, University Hospital Ostrava, Ostrava, Czech RepublicDepartment of Clinical Neurosciences, Faculty of Medicine, University of Ostrava, Ostrava, Czech RepublicFaculty of Medicine, Masaryk University, Brno, Czech RepublicDepartment of Laboratory Medicine, University Hospital Brno, Brno, Czech RepublicDepartment of Imaging Methods, Faculty of Medicine, University of Ostrava, Ostrava, Czech RepublicDepartment of Clinical Biochemistry, Institute of Laboratory Medicine, University Hospital Ostrava, Ostrava, Czech RepublicAim. The aim of this study was to identify whether NfL and CXCL13 cerebrospinal fluid (CSF) concentrations at diagnostic lumbar puncture can predict the course of multiple sclerosis (MS) in terms of relapses, higher expanded disability status scale (EDSS) and magnetic resonance imaging (MRI) activity. Methods. We conducted a single-centre prospective observational cohort study at the MS center, University Hospital Ostrava, Czech Republic. CSF NfL (cNfL) and CXCL13 concentrations were examined (ELISA method) in patients with clinically isolated syndrome (CIS) and relapsing-remitting MS (RRMS) at the time of diagnostic lumbar puncture. Results. A total of 44 patients with CIS or early RRMS were enrolled, 31 (70.5%) of whom were women. The median age at the time of CSF sampling was 31.21 years (IQR 25.43-39.32), and the follow-up period was 54.6 months (IQR 44.03-59.48). In the simple and multiple logistic regression models, CXCL13 levels did not predict relapses, MRI activity or EDSS > 2.5. Similarly, cNfL concentrations did not predict relapses or MRI activity in either model. In the multiple regression, higher cNfL levels were associated with reaching EDSS > 2.5 (odds ratio [OR] 1.002, 95% confidence interval [CI] 1.000 to 1.003). Conclusions. Our data did not confirm cNfL and/or CXCL13 CSF levels were predictive factors for disease activity such as relapses and MRI activity at the time of diagnostic lumbar puncture in patients with RRMS. While cNfL CSF levels predicted higher disability only after adjustment for other known risk factors, elevated CSF CXCL13 did not predict higher disability at all.https://biomed.papers.upol.cz/artkey/bio-202301-0005_cerebrospinal-fluid-neurofilament-light-chains-and-cxcl13-as-predictive-factors-for-clinical-course-of-multiple.phpmultiple sclerosisbiomarkersneurofilament light chaincxcl13clinical course
spellingShingle Pavel Hradilek
Kamila Zondra Revendova
Jana Horakova
Radovan Bunganic
Ondrej Pelisek
David Zeman
Pavla Hanzlikova
Pavlina Kusnierova
Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis
Biomedical Papers
multiple sclerosis
biomarkers
neurofilament light chain
cxcl13
clinical course
title Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis
title_full Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis
title_fullStr Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis
title_full_unstemmed Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis
title_short Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis
title_sort cerebrospinal fluid neurofilament light chains and cxcl13 as predictive factors for clinical course of multiple sclerosis
topic multiple sclerosis
biomarkers
neurofilament light chain
cxcl13
clinical course
url https://biomed.papers.upol.cz/artkey/bio-202301-0005_cerebrospinal-fluid-neurofilament-light-chains-and-cxcl13-as-predictive-factors-for-clinical-course-of-multiple.php
work_keys_str_mv AT pavelhradilek cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT kamilazondrarevendova cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT janahorakova cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT radovanbunganic cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT ondrejpelisek cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT davidzeman cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT pavlahanzlikova cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis
AT pavlinakusnierova cerebrospinalfluidneurofilamentlightchainsandcxcl13aspredictivefactorsforclinicalcourseofmultiplesclerosis