Protein-based classifier to predict conversion from clinically isolated syndrome to multiple sclerosis

Mostra el registre complet Registre parcial de l'ítem

  • dc.contributor.author Borrás, Evaca
  • dc.contributor.author Cantó, Esterca
  • dc.contributor.author Choi, Meenaca
  • dc.contributor.author Villar, Luisa Mariaca
  • dc.contributor.author Álvarez Cermeño, Jose Carlosca
  • dc.contributor.author Chiva, Cristinaca
  • dc.contributor.author Montalbán Gairín, Xavierca
  • dc.contributor.author Vitek, Olgaca
  • dc.contributor.author Comabella López, Manuelca
  • dc.contributor.author Sabidó Aguadé, Eduard, 1981-ca
  • dc.date.accessioned 2016-06-15T13:42:04Z
  • dc.date.available 2017-02-01T03:00:03Z
  • dc.date.issued 2016
  • dc.description.abstract Multiple sclerosis is an inflammatory, demyelinating, and neurodegenerative disease of the central nervous system. In most patients, the disease initiates with an episode of neurological disturbance referred to as clinically isolated syndrome, but not all patients with this syndrome develop multiple sclerosis over time, and currently, there is no clinical test that can conclusively establish whether a patient with a clinically isolated syndrome will eventually develop clinically defined multiple sclerosis. Here, we took advantage of the capabilities of targeted mass spectrometry to establish a diagnostic molecular classifier with high sensitivity and specificity able to differentiate between clinically isolated syndrome patients with a high and a low risk of developing multiple sclerosis. Based on the combination of abundances of proteins chitinase 3-like 1 and ala-β-his-dipeptidase in cerebrospinal fluid, we built a statistical model able to assign to each patient a precise probability of conversion to clinically defined multiple sclerosis. Our results are of special relevance for patients affected by multiple sclerosis as early treatment can prevent brain damage and slow down the disease progression.ca
  • dc.description.sponsorship This work was supported by a grant from the “Fondo de Investigación Sanitaria” (FIS) (grant number PI09/00788), Ministry of Science and Innovation, Spain. E.C. was supported by a contract from the FIS (contract number FI 09/00705), Ministry of Science and Innovation, Spain.
  • dc.format.mimetype application/pdfca
  • dc.identifier.citation Borràs E, Cantó E, Choi M, Maria Villar L, Álvarez-Cermeño JC, Chiva C et al. Protein-based classifier to predict conversion from clinically isolated syndrome to multiple sclerosis. Molecular & cellular proteomics. 2016; 15(1): 318-328. DOI 10.1074/mcp.M115.053256ca
  • dc.identifier.doi http://dx.doi.org/10.1074/mcp.M115.053256
  • dc.identifier.issn 1535-9476
  • dc.identifier.uri http://hdl.handle.net/10230/26919
  • dc.language.iso engca
  • dc.publisher American Society for Biochemistry and Molecular Biology (ASBMB)ca
  • dc.relation.ispartof Molecular & cellular proteomics. 2016; 15(1): 318-328
  • dc.rights © 2016 by The American Society for Biochemistry and Molecular Biology. This paper is available on line at http://www.mcponline.orgca
  • dc.rights.accessRights info:eu-repo/semantics/openAccess
  • dc.subject.other Esclerosi múltipleca
  • dc.title Protein-based classifier to predict conversion from clinically isolated syndrome to multiple sclerosisca
  • dc.type info:eu-repo/semantics/articleca
  • dc.type.version info:eu-repo/semantics/publishedVersionca