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Tau protein: a possible prognostic factor in optic neuritis and multiple sclerosis
Background: Tau protein has been proposed as biomarker of axonal damage leading to irreversible neurological impairment in MS. CSF concentrations may be useful when determining risk of progression from ON to MS. Objective: To investigate the association between tau protein concentration and 14-3-3 p...
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Published in: | Multiple sclerosis 2012-05, Vol.18 (5), p.592-599 |
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container_title | Multiple sclerosis |
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creator | Frederiksen, J Kristensen, K Bahl, JMC Christiansen, M |
description | Background: Tau protein has been proposed as biomarker of axonal damage leading to irreversible neurological impairment in MS. CSF concentrations may be useful when determining risk of progression from ON to MS.
Objective: To investigate the association between tau protein concentration and 14-3-3 protein in the cerebrospinal fluid (CSF) of patients with monosymptomatic optic neuritis (ON) versus patients with monosymptomatic onset who progressed to multiple sclerosis (MS). To evaluate results against data found in a complete literature review.
Methods: A total of 66 patients with MS and/or ON from the Department of Neurology of Glostrup Hospital, University of Copenhagen, Denmark, were included. CSF samples were analysed for tau protein and 14-3-3 protein, and clinical and paraclinical information was obtained from medical records.
Results: The study shows a significantly increased concentration of tau protein in CSF from patients with relapsing–remitting MS and patients monosymptomatic at onset who progressed to MS, but interestingly no increased tau protein concentration in monosymptomatic ON. The concentration of tau protein was significantly correlated to Expanded Disability Status Scale score. No 14-3-3 protein was detected in any CSF sample.
Conclusions: The results of this study invite further exploration of the possible role of tau protein as a prognostic factor to predict progression from ON to MS in future studies. |
doi_str_mv | 10.1177/1352458511424588 |
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Objective: To investigate the association between tau protein concentration and 14-3-3 protein in the cerebrospinal fluid (CSF) of patients with monosymptomatic optic neuritis (ON) versus patients with monosymptomatic onset who progressed to multiple sclerosis (MS). To evaluate results against data found in a complete literature review.
Methods: A total of 66 patients with MS and/or ON from the Department of Neurology of Glostrup Hospital, University of Copenhagen, Denmark, were included. CSF samples were analysed for tau protein and 14-3-3 protein, and clinical and paraclinical information was obtained from medical records.
Results: The study shows a significantly increased concentration of tau protein in CSF from patients with relapsing–remitting MS and patients monosymptomatic at onset who progressed to MS, but interestingly no increased tau protein concentration in monosymptomatic ON. The concentration of tau protein was significantly correlated to Expanded Disability Status Scale score. No 14-3-3 protein was detected in any CSF sample.
Conclusions: The results of this study invite further exploration of the possible role of tau protein as a prognostic factor to predict progression from ON to MS in future studies.</description><identifier>ISSN: 1352-4585</identifier><identifier>EISSN: 1477-0970</identifier><identifier>DOI: 10.1177/1352458511424588</identifier><identifier>PMID: 21969238</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>14-3-3 protein ; 14-3-3 Proteins - cerebrospinal fluid ; Adult ; Biological and medical sciences ; biomarkers ; Biomarkers - cerebrospinal fluid ; Brain - metabolism ; Cerebrospinal fluid ; Data processing ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Denmark ; Disability Evaluation ; Disease Progression ; Female ; Hospitals ; Hospitals, University ; Humans ; Male ; Medical sciences ; Middle Aged ; Multiple sclerosis ; Multiple Sclerosis - cerebrospinal fluid ; Multiple Sclerosis - diagnosis ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurological complications ; Neurology ; Optic neuritis ; Optic Neuritis - cerebrospinal fluid ; Optic Neuritis - diagnosis ; Prognosis ; Severity of Illness Index ; Tau protein ; tau Proteins - cerebrospinal fluid ; Time Factors ; Up-Regulation ; Young Adult</subject><ispartof>Multiple sclerosis, 2012-05, Vol.18 (5), p.592-599</ispartof><rights>The Author(s) 2012</rights><rights>2015 INIST-CNRS</rights><rights>SAGE Publications © May 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-d42e5e5c8bff65b9d54b957077014afe49d92ce251b993142e1876a56caa8a2a3</citedby><cites>FETCH-LOGICAL-c428t-d42e5e5c8bff65b9d54b957077014afe49d92ce251b993142e1876a56caa8a2a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79364</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26003448$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21969238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frederiksen, J</creatorcontrib><creatorcontrib>Kristensen, K</creatorcontrib><creatorcontrib>Bahl, JMC</creatorcontrib><creatorcontrib>Christiansen, M</creatorcontrib><title>Tau protein: a possible prognostic factor in optic neuritis and multiple sclerosis</title><title>Multiple sclerosis</title><addtitle>Mult Scler</addtitle><description>Background: Tau protein has been proposed as biomarker of axonal damage leading to irreversible neurological impairment in MS. CSF concentrations may be useful when determining risk of progression from ON to MS.
Objective: To investigate the association between tau protein concentration and 14-3-3 protein in the cerebrospinal fluid (CSF) of patients with monosymptomatic optic neuritis (ON) versus patients with monosymptomatic onset who progressed to multiple sclerosis (MS). To evaluate results against data found in a complete literature review.
Methods: A total of 66 patients with MS and/or ON from the Department of Neurology of Glostrup Hospital, University of Copenhagen, Denmark, were included. CSF samples were analysed for tau protein and 14-3-3 protein, and clinical and paraclinical information was obtained from medical records.
Results: The study shows a significantly increased concentration of tau protein in CSF from patients with relapsing–remitting MS and patients monosymptomatic at onset who progressed to MS, but interestingly no increased tau protein concentration in monosymptomatic ON. The concentration of tau protein was significantly correlated to Expanded Disability Status Scale score. No 14-3-3 protein was detected in any CSF sample.
Conclusions: The results of this study invite further exploration of the possible role of tau protein as a prognostic factor to predict progression from ON to MS in future studies.</description><subject>14-3-3 protein</subject><subject>14-3-3 Proteins - cerebrospinal fluid</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>biomarkers</subject><subject>Biomarkers - cerebrospinal fluid</subject><subject>Brain - metabolism</subject><subject>Cerebrospinal fluid</subject><subject>Data processing</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Denmark</subject><subject>Disability Evaluation</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Hospitals</subject><subject>Hospitals, University</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - cerebrospinal fluid</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurological complications</subject><subject>Neurology</subject><subject>Optic neuritis</subject><subject>Optic Neuritis - cerebrospinal fluid</subject><subject>Optic Neuritis - diagnosis</subject><subject>Prognosis</subject><subject>Severity of Illness Index</subject><subject>Tau protein</subject><subject>tau Proteins - cerebrospinal fluid</subject><subject>Time Factors</subject><subject>Up-Regulation</subject><subject>Young Adult</subject><issn>1352-4585</issn><issn>1477-0970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkUtL9TAQhoMo3veupCAfuKlmmqRp3H2INxAE0XWZpqlEetqaaRf-e1PP8YIguJpk5nnnwsvYAfATAK1PQahMqkIByDkWa2wbpNYpN5qvx3csp3N9i-0QPXPOtRZqk21lYHKTiWKb3T_glAyhH53vzhJMhp7IV62bc09dT6O3SYN27EPiu6Qf5n_npuBHTwl2dbKY2tEPUUC2daEnT3tso8GW3P4q7rLHy4uH8-v09u7q5vz_bWplVoxpLTOnnLJF1TS5qkytZGWUjitykNg4aWqTWZcpqIwR8UAHhc5R5RaxwAzFLjte9o2rvkyOxnLhybq2xc71E5UQ-wCXgou_oDwXhQAd0aMf6HM_hS4e8k5pAOA8UnxJ2XgyBdeUQ_ALDK8RKmdryp_WRMnhqvFULVz9KfjwIgL_VgCSxbYJ2FlPX1we50o5c-mSI3xy37f7ZfAbrtGhNA</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>Frederiksen, J</creator><creator>Kristensen, K</creator><creator>Bahl, JMC</creator><creator>Christiansen, M</creator><general>SAGE Publications</general><general>Sage Publications</general><general>Sage Publications Ltd</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20120501</creationdate><title>Tau protein: a possible prognostic factor in optic neuritis and multiple sclerosis</title><author>Frederiksen, J ; Kristensen, K ; Bahl, JMC ; Christiansen, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-d42e5e5c8bff65b9d54b957077014afe49d92ce251b993142e1876a56caa8a2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>14-3-3 protein</topic><topic>14-3-3 Proteins - cerebrospinal fluid</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>biomarkers</topic><topic>Biomarkers - cerebrospinal fluid</topic><topic>Brain - metabolism</topic><topic>Cerebrospinal fluid</topic><topic>Data processing</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Denmark</topic><topic>Disability Evaluation</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Hospitals</topic><topic>Hospitals, University</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - cerebrospinal fluid</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurological complications</topic><topic>Neurology</topic><topic>Optic neuritis</topic><topic>Optic Neuritis - cerebrospinal fluid</topic><topic>Optic Neuritis - diagnosis</topic><topic>Prognosis</topic><topic>Severity of Illness Index</topic><topic>Tau protein</topic><topic>tau Proteins - cerebrospinal fluid</topic><topic>Time Factors</topic><topic>Up-Regulation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frederiksen, J</creatorcontrib><creatorcontrib>Kristensen, K</creatorcontrib><creatorcontrib>Bahl, JMC</creatorcontrib><creatorcontrib>Christiansen, M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Multiple sclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frederiksen, J</au><au>Kristensen, K</au><au>Bahl, JMC</au><au>Christiansen, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tau protein: a possible prognostic factor in optic neuritis and multiple sclerosis</atitle><jtitle>Multiple sclerosis</jtitle><addtitle>Mult Scler</addtitle><date>2012-05-01</date><risdate>2012</risdate><volume>18</volume><issue>5</issue><spage>592</spage><epage>599</epage><pages>592-599</pages><issn>1352-4585</issn><eissn>1477-0970</eissn><abstract>Background: Tau protein has been proposed as biomarker of axonal damage leading to irreversible neurological impairment in MS. CSF concentrations may be useful when determining risk of progression from ON to MS.
Objective: To investigate the association between tau protein concentration and 14-3-3 protein in the cerebrospinal fluid (CSF) of patients with monosymptomatic optic neuritis (ON) versus patients with monosymptomatic onset who progressed to multiple sclerosis (MS). To evaluate results against data found in a complete literature review.
Methods: A total of 66 patients with MS and/or ON from the Department of Neurology of Glostrup Hospital, University of Copenhagen, Denmark, were included. CSF samples were analysed for tau protein and 14-3-3 protein, and clinical and paraclinical information was obtained from medical records.
Results: The study shows a significantly increased concentration of tau protein in CSF from patients with relapsing–remitting MS and patients monosymptomatic at onset who progressed to MS, but interestingly no increased tau protein concentration in monosymptomatic ON. The concentration of tau protein was significantly correlated to Expanded Disability Status Scale score. No 14-3-3 protein was detected in any CSF sample.
Conclusions: The results of this study invite further exploration of the possible role of tau protein as a prognostic factor to predict progression from ON to MS in future studies.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>21969238</pmid><doi>10.1177/1352458511424588</doi><tpages>8</tpages></addata></record> |
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subjects | 14-3-3 protein 14-3-3 Proteins - cerebrospinal fluid Adult Biological and medical sciences biomarkers Biomarkers - cerebrospinal fluid Brain - metabolism Cerebrospinal fluid Data processing Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Denmark Disability Evaluation Disease Progression Female Hospitals Hospitals, University Humans Male Medical sciences Middle Aged Multiple sclerosis Multiple Sclerosis - cerebrospinal fluid Multiple Sclerosis - diagnosis Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neurological complications Neurology Optic neuritis Optic Neuritis - cerebrospinal fluid Optic Neuritis - diagnosis Prognosis Severity of Illness Index Tau protein tau Proteins - cerebrospinal fluid Time Factors Up-Regulation Young Adult |
title | Tau protein: a possible prognostic factor in optic neuritis and multiple sclerosis |
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