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The impact of C677T and A1298C MTHFR polymorphisms on methotrexate therapeutic response in East Bohemian region rheumatoid arthritis patients

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F15%3A10294691" target="_blank" >RIV/00216208:11320/15:10294691 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/15:10294691 RIV/00216208:11160/15:10294691 RIV/00179906:_____/15:10294691

  • Result on the web

    <a href="http://link.springer.com/article/10.1007/s00296-015-3219-z/fulltext.html" target="_blank" >http://link.springer.com/article/10.1007/s00296-015-3219-z/fulltext.html</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00296-015-3219-z" target="_blank" >10.1007/s00296-015-3219-z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The impact of C677T and A1298C MTHFR polymorphisms on methotrexate therapeutic response in East Bohemian region rheumatoid arthritis patients

  • Original language description

    Some single-nucleotide polymorphisms (SNPs) might be predictive of methotrexate (MTX) therapeutic outcome in rheumatoid arthritis (RA). The aim of this study was to determine whether SNPs in the methylenetetrahydrofolate reductase (MTHFR) gene are predictive of MTX response. Comparison was made using EULAR response criteria and according to the change of DAS28 (DeltaDAS28) after a 6-month MTX treatment in RA patient cohort. The two SNPs C677T (rs1801133) and A1298C (rs1801131) have been genotyped. A total of 120 patients were enrolled in the study, and all of them fulfilled the American College of Rheumatology 1987 RA criteria and are currently or previously taking MTX oral treatment, either as a monotherapy (n=65) or in a combination with other disease-modifying antirheumatic drugs (n=55). Genotyping was performed using qPCR allelic discrimination. We did not found any association of C677T and A1298C genotypes with MTX treatment inefficacy in dominant model (OR 1.23, 95 % CI 0.57-2.65

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FE - Other fields of internal medicine

  • OECD FORD branch

Result continuities

  • Project

  • 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

    Rheumatology International

  • ISSN

    0172-8172

  • e-ISSN

  • Volume of the periodical

    35

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    13

  • Pages from-to

    1149-1161

  • UT code for WoS article

    000354709500005

  • EID of the result in the Scopus database

    2-s2.0-84929839397