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Distribution of HLA-DQB1 in Czech Patients with Central Hypersomnias

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F16%3A10337401" target="_blank" >RIV/00064165:_____/16:10337401 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/16:10337401 RIV/00023736:_____/16:00011723

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s00005-016-0435-5" target="_blank" >http://dx.doi.org/10.1007/s00005-016-0435-5</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00005-016-0435-5" target="_blank" >10.1007/s00005-016-0435-5</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Distribution of HLA-DQB1 in Czech Patients with Central Hypersomnias

  • Original language description

    The aim of our study was to analyze the distribution of HLA-DQB1 in Czech patients with central hypersomnias and differences between diagnostic groups of narcolepsy type 1 (NT1), type 2 (NT2), idiopathic hypersomnia (IH) and no central hypersomnia subjects (no-CH). Statistical analysis of DQB1 genotyping was performed on the cohort of 716 patients (375 men, 341 women) with reported excessive daytime sleepiness. DQB1*06:02 allele was present in 94% of the NT1 patients. The decrease of DQB1*06:03 allele was also confirmed. No other DQB1*06 allele nor any other DQB1 allele group was differently distributed in the NT1. In the cohort of NT2 patients DQB1*06:02 allele was present in 43%. Allele group DQB*05 was detected with a significantly higher frequency in this diagnostic unit. Any differences in presence of DQB1*05 alleles in NT2 patients were not reported so far. The cohort of patients with IH did not show any difference in allele distribution of DQB1 alleles/allele groups comparing to healthy controls. DQB1*06:02 allele was significantly increased in the no hypersomnia group. No other DQB1 allele/allele group had any difference in distribution in patients comparing to healthy controls. The different distribution of DQB1*06:02 and other DQB1 alleles/allele groups was detected in analyzed diagnostic groups. These results indicate that DQB1 contributes to the genetic predisposition to NT1, NT2, IH and no-CH in different manners.

  • 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

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Archivum Immunologiae et Therapiae Experimentalis

  • ISSN

    0004-069X

  • e-ISSN

  • Volume of the periodical

    64

  • Issue of the periodical within the volume

    Suppl. 1

  • Country of publishing house

    PL - POLAND

  • Number of pages

    10

  • Pages from-to

    89-98

  • UT code for WoS article

  • EID of the result in the Scopus database

    2-s2.0-85009278991