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Interactive effect of MTHFR and ADRA2A gene polymorphisms on pathogenesis of schizophrenia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F13%3A00071796" target="_blank" >RIV/00216224:14310/13:00071796 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985904:_____/13:00428603 RIV/61988987:17110/13:A1501A3S

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Interactive effect of MTHFR and ADRA2A gene polymorphisms on pathogenesis of schizophrenia

  • Original language description

    Increasing evidences support the importance of epigenetic control in schizophrenia pathogenesis. One of the enzymes involved in DNA methylation process through homocysteine metabolism is methylenetetrahydrofolate reductase (MTHFR). The most extensively studied variant in the MTHFR gene is the C677T polymorphism, resulting in reduced enzyme activity and elevated homocysteine level. Methods: In sample of 192 schizophrenics and 213 healthy controls an increasing risk of schizophrenia associated with MTHFR677 CT + TT genotype was found (OR=1.6, P=0.021). Association was also evaluated by considering the C677T polymorphism as an interaction with COMT Val158Met and ADRA2A C-1291G polymorphisms previously associated with schizophrenia risk using a logistic regression analysis. Results: Previous studies of MTHFR*COMT (C677T*Val158Met) interaction in relation to schizophrenia resulted in inconsistent results.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    ED - Physiology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT14504" target="_blank" >NT14504: Epidemiology and genetics of schizophrenia</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Neuroendocrinology Letters

  • ISSN

    0172-780X

  • e-ISSN

  • Volume of the periodical

    34

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    LU - LUXEMBOURG

  • Number of pages

    6

  • Pages from-to

    792-797

  • UT code for WoS article

    000331786100010

  • EID of the result in the Scopus database