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Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis
INTRODUCTION: Multiple sclerosis (MS) pathophysiology comprises both inflammatory and neurodegenerative characteristics. Cerebrospinal fluid (CSF) analysis allows for assessment of inflammation while neurofilament light chain can indicate neuroaxonal damage. Retinal thinning is a robust prognostic b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936502/ https://www.ncbi.nlm.nih.gov/pubmed/35321514 http://dx.doi.org/10.3389/fneur.2022.814734 |
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author | Krajnc, Nik Altmann, Patrick Riedl, Katharina Mitsch, Christoph Berger, Thomas Leutmezer, Fritz Rommer, Paulus Pemp, Berthold Bsteh, Gabriel |
author_facet | Krajnc, Nik Altmann, Patrick Riedl, Katharina Mitsch, Christoph Berger, Thomas Leutmezer, Fritz Rommer, Paulus Pemp, Berthold Bsteh, Gabriel |
author_sort | Krajnc, Nik |
collection | PubMed |
description | INTRODUCTION: Multiple sclerosis (MS) pathophysiology comprises both inflammatory and neurodegenerative characteristics. Cerebrospinal fluid (CSF) analysis allows for assessment of inflammation while neurofilament light chain can indicate neuroaxonal damage. Retinal thinning is a robust prognostic biomarker for neurodegeneration in MS. To date, an association between CSF parameters upon MS diagnosis and retinal thinning has not been investigated. AIMS AND OBJECTIVES: We aimed to determine whether CSF parameters are associated with the evolution of retinal layer thinning in people with MS (pwMS). METHODS: For this longitudinal observational study, we investigated pwMS from the Vienna MS database (VMSD), who had undergone (1) a diagnostic lumbar puncture (LP) between 2015 and 2020, and (2) simultaneous optical coherence tomography (OCT) and/or (3) a follow-up OCT scan. Linear stepwise regression models were calculated with OCT parameters (peripapillary retinal nerve fiber layer [pRNFL] thickness at LP and at follow-up, annualized loss of pRNFL thickness [aLpRNFL]) as a dependent variable, and CSF parameters (white blood cell [WBC] count, total protein [(CSF)TP], CSF/serum albumin ratio [Q(alb)], intrathecal synthesis of immunoglobulins, neurofilament light chain [NfL] in both CSF and serum [(CSF)NfL/sNfL]) as independent variables adjusted for age, sex, and disease duration. RESULTS: We analyzed 61 pwMS (median age 30.0 years [interquartile range 25.5–35.0], 57.4% female, median disease duration 1.0 month [IQR 0–2.0] before LP, median follow-up 1.9 years [IQR 1.1–3.5]). (CSF)NfL and sNfL measurements were available in 26 and 31 pwMS, respectively. pRNFL thickness at LP was inversely associated with the CSF WBC count (β = −0.36; 95% CI −0.51, −0.08; p = 0.008). We did not find any association between other CSF parameters, including (CSF)NfL, sNfL, and aLpRNFL. CONCLUSIONS: Increased WBC count as an indicator of acute inflammation and blood-brain-barrier breakdown seems to be associated with the amount of retinal thickness already lost at the time of LP. However, neither routine CSF parameters nor a singular NfL measurement allows the prediction of future retinal thinning. |
format | Online Article Text |
id | pubmed-8936502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89365022022-03-22 Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis Krajnc, Nik Altmann, Patrick Riedl, Katharina Mitsch, Christoph Berger, Thomas Leutmezer, Fritz Rommer, Paulus Pemp, Berthold Bsteh, Gabriel Front Neurol Neurology INTRODUCTION: Multiple sclerosis (MS) pathophysiology comprises both inflammatory and neurodegenerative characteristics. Cerebrospinal fluid (CSF) analysis allows for assessment of inflammation while neurofilament light chain can indicate neuroaxonal damage. Retinal thinning is a robust prognostic biomarker for neurodegeneration in MS. To date, an association between CSF parameters upon MS diagnosis and retinal thinning has not been investigated. AIMS AND OBJECTIVES: We aimed to determine whether CSF parameters are associated with the evolution of retinal layer thinning in people with MS (pwMS). METHODS: For this longitudinal observational study, we investigated pwMS from the Vienna MS database (VMSD), who had undergone (1) a diagnostic lumbar puncture (LP) between 2015 and 2020, and (2) simultaneous optical coherence tomography (OCT) and/or (3) a follow-up OCT scan. Linear stepwise regression models were calculated with OCT parameters (peripapillary retinal nerve fiber layer [pRNFL] thickness at LP and at follow-up, annualized loss of pRNFL thickness [aLpRNFL]) as a dependent variable, and CSF parameters (white blood cell [WBC] count, total protein [(CSF)TP], CSF/serum albumin ratio [Q(alb)], intrathecal synthesis of immunoglobulins, neurofilament light chain [NfL] in both CSF and serum [(CSF)NfL/sNfL]) as independent variables adjusted for age, sex, and disease duration. RESULTS: We analyzed 61 pwMS (median age 30.0 years [interquartile range 25.5–35.0], 57.4% female, median disease duration 1.0 month [IQR 0–2.0] before LP, median follow-up 1.9 years [IQR 1.1–3.5]). (CSF)NfL and sNfL measurements were available in 26 and 31 pwMS, respectively. pRNFL thickness at LP was inversely associated with the CSF WBC count (β = −0.36; 95% CI −0.51, −0.08; p = 0.008). We did not find any association between other CSF parameters, including (CSF)NfL, sNfL, and aLpRNFL. CONCLUSIONS: Increased WBC count as an indicator of acute inflammation and blood-brain-barrier breakdown seems to be associated with the amount of retinal thickness already lost at the time of LP. However, neither routine CSF parameters nor a singular NfL measurement allows the prediction of future retinal thinning. Frontiers Media S.A. 2022-03-07 /pmc/articles/PMC8936502/ /pubmed/35321514 http://dx.doi.org/10.3389/fneur.2022.814734 Text en Copyright © 2022 Krajnc, Altmann, Riedl, Mitsch, Berger, Leutmezer, Rommer, Pemp and Bsteh. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Krajnc, Nik Altmann, Patrick Riedl, Katharina Mitsch, Christoph Berger, Thomas Leutmezer, Fritz Rommer, Paulus Pemp, Berthold Bsteh, Gabriel Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis |
title | Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis |
title_full | Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis |
title_fullStr | Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis |
title_full_unstemmed | Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis |
title_short | Association of Cerebrospinal Fluid Parameters and Neurofilament Light Chain With Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis |
title_sort | association of cerebrospinal fluid parameters and neurofilament light chain with retinal nerve fiber layer thickness in multiple sclerosis |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936502/ https://www.ncbi.nlm.nih.gov/pubmed/35321514 http://dx.doi.org/10.3389/fneur.2022.814734 |
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