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
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Czech description
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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
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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 & Neuroinflammation
ISSN
2332-7812
e-ISSN
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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
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UT code for WoS article
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EID of the result in the Scopus database
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