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Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?

OBJECTIVE: To investigate whether neurofilament light polypeptide (NfL) level in cerebrospinal fluid (CSF), currently a prognostic biomarker of neurodegeneration in patients with multiple sclerosis (MS), may be a potential biomarker of cognitive dysfunction in MS. METHODS: This observational case–co...

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Autores principales: Kalatha, Thaleia, Arnaoutoglou, Marianthi, Koukoulidis, Theodoros, Hatzifilippou, Eleni, Bouras, Emmanouil, Baloyannis, Stavros, Koutsouraki, Effrosyni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567748/
https://www.ncbi.nlm.nih.gov/pubmed/30982375
http://dx.doi.org/10.1177/0300060519840550
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author Kalatha, Thaleia
Arnaoutoglou, Marianthi
Koukoulidis, Theodoros
Hatzifilippou, Eleni
Bouras, Emmanouil
Baloyannis, Stavros
Koutsouraki, Effrosyni
author_facet Kalatha, Thaleia
Arnaoutoglou, Marianthi
Koukoulidis, Theodoros
Hatzifilippou, Eleni
Bouras, Emmanouil
Baloyannis, Stavros
Koutsouraki, Effrosyni
author_sort Kalatha, Thaleia
collection PubMed
description OBJECTIVE: To investigate whether neurofilament light polypeptide (NfL) level in cerebrospinal fluid (CSF), currently a prognostic biomarker of neurodegeneration in patients with multiple sclerosis (MS), may be a potential biomarker of cognitive dysfunction in MS. METHODS: This observational case–control study included patients with MS. CSF levels of NfL were determined using enzyme-linked immunosorbent assay. Cognitive function was measured with the Brief International Cognitive Assessment for MS (BICAMS) battery and Paced Auditory Serial Addition Test (PASAT3), standardized to the Greek population. RESULTS: Of 39 patients enrolled (aged 42.7 ± 13.6 years), 36% were classified as cognitively impaired according to BICAMS z-scores (–0.34 ± 1.13). Relapsing MS was significantly better than progressive forms regarding BICAMS z-score (mean difference [MD] 1.39; 95% confidence interval [CI] 0.54, 2.24), Symbol Digit Modality Test score (MD 1.73; 95% CI 0.46, 3.0) and Greek Verbal Learning Test (MD 1.77; 95% CI 0.82, 2.72). An inversely proportional association between CSF NfL levels and BICAMS z-scores was found in progressive forms of MS (r(p) = –0.944). CONCLUSIONS: This study provides preliminary evidence for an association between CSF NfL levels and cognition in progressive forms of MS, which requires validation in larger samples.
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spelling pubmed-65677482019-06-20 Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis? Kalatha, Thaleia Arnaoutoglou, Marianthi Koukoulidis, Theodoros Hatzifilippou, Eleni Bouras, Emmanouil Baloyannis, Stavros Koutsouraki, Effrosyni J Int Med Res Clinical Research Reports OBJECTIVE: To investigate whether neurofilament light polypeptide (NfL) level in cerebrospinal fluid (CSF), currently a prognostic biomarker of neurodegeneration in patients with multiple sclerosis (MS), may be a potential biomarker of cognitive dysfunction in MS. METHODS: This observational case–control study included patients with MS. CSF levels of NfL were determined using enzyme-linked immunosorbent assay. Cognitive function was measured with the Brief International Cognitive Assessment for MS (BICAMS) battery and Paced Auditory Serial Addition Test (PASAT3), standardized to the Greek population. RESULTS: Of 39 patients enrolled (aged 42.7 ± 13.6 years), 36% were classified as cognitively impaired according to BICAMS z-scores (–0.34 ± 1.13). Relapsing MS was significantly better than progressive forms regarding BICAMS z-score (mean difference [MD] 1.39; 95% confidence interval [CI] 0.54, 2.24), Symbol Digit Modality Test score (MD 1.73; 95% CI 0.46, 3.0) and Greek Verbal Learning Test (MD 1.77; 95% CI 0.82, 2.72). An inversely proportional association between CSF NfL levels and BICAMS z-scores was found in progressive forms of MS (r(p) = –0.944). CONCLUSIONS: This study provides preliminary evidence for an association between CSF NfL levels and cognition in progressive forms of MS, which requires validation in larger samples. SAGE Publications 2019-04-14 2019-05 /pmc/articles/PMC6567748/ /pubmed/30982375 http://dx.doi.org/10.1177/0300060519840550 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Clinical Research Reports
Kalatha, Thaleia
Arnaoutoglou, Marianthi
Koukoulidis, Theodoros
Hatzifilippou, Eleni
Bouras, Emmanouil
Baloyannis, Stavros
Koutsouraki, Effrosyni
Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?
title Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?
title_full Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?
title_fullStr Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?
title_full_unstemmed Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?
title_short Does cognitive dysfunction correlate with neurofilament light polypeptide levels in the CSF of patients with multiple sclerosis?
title_sort does cognitive dysfunction correlate with neurofilament light polypeptide levels in the csf of patients with multiple sclerosis?
topic Clinical Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567748/
https://www.ncbi.nlm.nih.gov/pubmed/30982375
http://dx.doi.org/10.1177/0300060519840550
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