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Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F15%3A10312820" target="_blank" >RIV/00216208:11110/15:10312820 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064165:_____/15:10312820

  • Result on the web

    <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360800/pdf/NEURIMMINFL2014003087.pdf" target="_blank" >http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360800/pdf/NEURIMMINFL2014003087.pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1212/NXI.0000000000000081" target="_blank" >10.1212/NXI.0000000000000081</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children

  • Original language description

    Objective: To determine whether myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) were predictive of a demyelination phenotype in children presenting with acquired demyelinating syndrome (ADS). Method: Sixty-five children with a first episode of ADS (12 acute disseminated encephalomyelitis, 24 optic neuritis, 18 transverse myelitis, 11 other clinically isolated syndrome) were identified from 2 national demyelination programs in the United Kingdom and France. Acute serum samples were tested for MOG-Abs by cell-based assay. Antibodies were used to predict diagnosis of multiple sclerosis (MS) at 1 year. Results: Twenty-three of 65 (35%) children had MOG-Abs. Antibody-positive and antibodynegative patients were not clinically different at presentation, but identification of MOG-Abs predicted a non-MS course at 1-year follow-up: only 2/23 (9%) MOG-Ab-positive patients were diagnosed with MS compared to 16/42 (38%) MOG-Ab-negative patients (p 5 0.019, Fisher exact test). Antibody posi

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FH - Neurology, neuro-surgery, nuero-sciences

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT13239" target="_blank" >NT13239: Phenotypes of axonal injury in multiple sclerosis based on in vivo measures of retinal pathology using optical coherence tomography</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Neurology: Neuroimmunology &amp; Neuroinflammation

  • ISSN

    2332-7812

  • e-ISSN

  • Volume of the periodical

    2

  • Issue of the periodical within the volume

    March

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

  • UT code for WoS article

  • EID of the result in the Scopus database