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dc.contributor.authorKroksveen, Ann Cathrineen_US
dc.contributor.authorAasebø, Eliseen_US
dc.contributor.authorVethe, Heidrunen_US
dc.contributor.authorvan Pesch, Vincenten_US
dc.contributor.authorFranciotta, Diegoen_US
dc.contributor.authorTeunissen, Charlotte E.en_US
dc.contributor.authorUlvik, Rune Johanen_US
dc.contributor.authorVedeler, Christian A.en_US
dc.contributor.authorMyhr, Kjell-Mortenen_US
dc.contributor.authorBarsnes, Haralden_US
dc.contributor.authorBerven, Frodeen_US
dc.date.accessioned2017-11-20T08:33:56Z
dc.date.available2017-11-20T08:33:56Z
dc.date.issued2013-01
dc.PublishedKroksveen AC, Aasebø E, Vethe H, van Pesch V, Franciotta D, Teunissen CE, Ulvik RJ, Vedeler CA, Myhr K, Barsnes H, Berven F. Discovery and initial verification of differentially abundant proteins between multiple sclerosis patients and controls using iTRAQ and SID-SRM. Journal of Proteomics. 2013;78:312-325eng
dc.identifier.issn1874-3919
dc.identifier.issn1876-7737
dc.identifier.urihttps://hdl.handle.net/1956/16942
dc.description.abstractIn the present study, we aimed to discover cerebrospinal fluid (CSF) proteins with significant abundance difference between early multiple sclerosis patients and controls, and do an initial verification of these proteins using selected reaction monitoring (SRM). iTRAQ and Orbitrap MS were used to compare the CSF proteome of patients with clinically isolated syndrome (CIS) (n = 5), patients with relapsing–remitting multiple sclerosis that had CIS at the time of lumbar puncture (n = 5), and controls with other inflammatory neurological disease (n = 5). Of more than 1200 identified proteins, five proteins were identified with significant abundance difference between the patients and controls. In the initial verification using SRM we analyzed a larger patient and control cohort (n = 132) and also included proteins reported as differentially abundant in multiple sclerosis in the literature. We found significant abundance difference for 11 proteins after verification, of which the five proteins alpha-1-antichymotrypsin, contactin-1, apolipoprotein D, clusterin, and kallikrein-6 were significantly differentially abundant in several of the group comparisons. This initial study form the basis for further biomarker verification studies in even larger sample cohorts, to determine if these proteins have relevance as diagnostic or prognostic biomarkers for multiple sclerosis.en_US
dc.language.isoengeng
dc.publisherElseviereng
dc.rightsAll rights reserved.eng
dc.subjectMultiple sclerosiseng
dc.subjectCerebrospinal fluideng
dc.subjectSelected reaction monitoringeng
dc.subjectQuantitative mass spectrometryeng
dc.titleDiscovery and initial verification of differentially abundant proteins between multiple sclerosis patients and controls using iTRAQ and SID-SRMen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2017-09-06T14:33:14Z
dc.description.versionacceptedVersionen_US
dc.rights.holderCopyright 2012 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.jprot.2012.09.037
dc.identifier.cristin1029256
dc.source.journalJournal of Proteomics
dc.source.4078
dc.source.pagenumber312-325
dc.relation.projectNorges forskningsråd: 204833
dc.subject.nsiVDP::Medisinske fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk biokjemi: 726
dc.subject.nsiVDP::Midical sciences: 700::Basic medical, dental and veterinary sciences: 710::Medical biochemistry: 726
dc.subject.nsiVDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Nevrologi: 752
dc.subject.nsiVDP::Midical sciences: 700::Clinical medical sciences: 750::Neurology: 752
dc.subject.nsiVDP::Medisinske Fag: 700en_US


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