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Oxidized glycerophosphatidylcholines in diabetes through non-targeted metabolomics: Their annotation and biological meaning

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    SYSNO ASEP0505648
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleOxidized glycerophosphatidylcholines in diabetes through non-targeted metabolomics: Their annotation and biological meaning
    Author(s) Godzien, J. (ES)
    Kalaska, B. (PL)
    Adamska-Patruno, E. (PL)
    Široká, Jitka (UEB-Q) ORCID
    Ciborowski, M. (PL)
    Kretowski, A. (PL)
    Barbas, C. (ES)
    Number of authors7
    Source TitleJournal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences. - : Elsevier - ISSN 1570-0232
    Roč. 1120, JUL 1 (2019), s. 62-70
    Number of pages9 s.
    Languageeng - English
    CountryNL - Netherlands
    KeywordsLong chain oxidized glycerophosphatidylcholines ; Metabolomics ; oxGPCs ; Oxidation ; t2dm
    Subject RIVCE - Biochemistry
    OECD categoryBiochemistry and molecular biology
    R&D ProjectsEF16_019/0000827 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUEB-Q - RVO:61389030
    UT WOS000470042300008
    EID SCOPUS85065030133
    DOI10.1016/j.jchromb.2019.04.053
    AnnotationLipid oxidation is one of the most important processes occurring in living cells and has been investigated through stable end-products. Currently, new insights into many physiological and pathophysiological processes provide a measurement of the first products of oxidation, e.g., oxidized glycerophosphatidylcholines (oxGPCs). Here, we evaluate the capacity of untargeted global metabolomics to measure oxGPCs in serum samples. This evaluation covered analytical reproducibility and data quality as well as the ability to capture metabolic alterations in diverse conditions. The analytical evaluation was performed based on the quality control samples, while the comparative analysis was based on the model of the development of type 2 diabetes mellitus (T2DM). The novelty of this approach arises not only from the measurement of oxGPCs instead of lipid peroxide-derived aldehydes but also from the stratification of the patients according to body mass index (BMI). Such a scenario was dictated by the fact that, despite the well-known relationship between obesity and T2DM development, there are lean individuals suffering from T2DM as well as obese people with normal glucose homeostasis. Our results provided evidence to support the ability of nontargeted metabolomics to measure oxGPCs. Comparative analysis of measured oxGPCs revealed differences in the level of oxGPCs either between different stages of disease development (insulin resistance, prediabetes) or BMI groups (normal weight, overweight, obese). The obtained results provided new insights into the metabolic processes leading to the development of T2DM and opened new paths in the investigation of the impact of body mass in T2DM progress.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2020
    Electronic addresshttp://doi.org/10.1016/j.jchromb.2019.04.053
Number of the records: 1  

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