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Comparison of two methods for dimethylarginines quantification

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00669806%3A_____%2F24%3A10477054" target="_blank" >RIV/00669806:_____/24:10477054 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216208:11140/24:10477054

  • Výsledek na webu

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=YnesWtWrin" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=YnesWtWrin</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.plabm.2024.e00359" target="_blank" >10.1016/j.plabm.2024.e00359</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Comparison of two methods for dimethylarginines quantification

  • Popis výsledku v původním jazyce

    Objectives: Both dimethylarginines are widely bound to chronic kidney disease (CKD). This study was focused to validate published LC-MS/MS method and compared the measured data with an immunoassay. Design and methods: The analysis was performed on a Dionex UltiMate 3000 UHPLC-Standard (Thermo Fisher Scientific, Waltham, Massachusetts, USA) with an amaZon SL ion trap (Bruker, Billerica, Massachusetts, USA). Comparison was evaluated by using Passing Bablok regression and Bland Altman plot. Healthy volunteers (n = 40) were used for validation and as control group to patients group (n = 40) with different stages of CKD. Results: The results in healthy controls determined by the LC-MS/MS (ELISA) method were 0.52 +- 0.0892 with 95 % CI: 0.49-0.55 (0.61 +- 0.1213 with 95 % CI: 0.57-0.64) μmol/L for AD MA and 0.56 +- 0.0810 with 95 % CI: 0.53-0.58 (0.62 +- 0.0752 with 95 % CI: 0.57-0.65) μmol/L for SDMA. In the same way, the patient group values determined by the LC-MS/MS (ELISA) method were 0.82 +- 0.1604 with 95 % CI: 0.75-0.88 (1.06 +- 0.3002 with 95 % CI: 0.94-1.19) μmol/L and 2.14 +- 0.8778 with 95 % CI: 1.47-2.58 (1.65 +- 0.5160 with 95 % CI: 1.40-1.98) μmol/L for ADMA and SDMA, respectively. The correlation between the methods, expressed as the Spearman correlation coefficient (R), was 0.858 (0.8059) for ADMA (p &lt; 0.0001) and 0.895 (0.9607) for SDMA (p &lt; 0.0001). Conclusions: ADMA levels determined by the immunoassay were almost 30 % overestimated, in contrast to SDMA levels, which were 3 % underestimated. According to our findings, a better correlation could be obtained by simple sample dilution.

  • Název v anglickém jazyce

    Comparison of two methods for dimethylarginines quantification

  • Popis výsledku anglicky

    Objectives: Both dimethylarginines are widely bound to chronic kidney disease (CKD). This study was focused to validate published LC-MS/MS method and compared the measured data with an immunoassay. Design and methods: The analysis was performed on a Dionex UltiMate 3000 UHPLC-Standard (Thermo Fisher Scientific, Waltham, Massachusetts, USA) with an amaZon SL ion trap (Bruker, Billerica, Massachusetts, USA). Comparison was evaluated by using Passing Bablok regression and Bland Altman plot. Healthy volunteers (n = 40) were used for validation and as control group to patients group (n = 40) with different stages of CKD. Results: The results in healthy controls determined by the LC-MS/MS (ELISA) method were 0.52 +- 0.0892 with 95 % CI: 0.49-0.55 (0.61 +- 0.1213 with 95 % CI: 0.57-0.64) μmol/L for AD MA and 0.56 +- 0.0810 with 95 % CI: 0.53-0.58 (0.62 +- 0.0752 with 95 % CI: 0.57-0.65) μmol/L for SDMA. In the same way, the patient group values determined by the LC-MS/MS (ELISA) method were 0.82 +- 0.1604 with 95 % CI: 0.75-0.88 (1.06 +- 0.3002 with 95 % CI: 0.94-1.19) μmol/L and 2.14 +- 0.8778 with 95 % CI: 1.47-2.58 (1.65 +- 0.5160 with 95 % CI: 1.40-1.98) μmol/L for ADMA and SDMA, respectively. The correlation between the methods, expressed as the Spearman correlation coefficient (R), was 0.858 (0.8059) for ADMA (p &lt; 0.0001) and 0.895 (0.9607) for SDMA (p &lt; 0.0001). Conclusions: ADMA levels determined by the immunoassay were almost 30 % overestimated, in contrast to SDMA levels, which were 3 % underestimated. According to our findings, a better correlation could be obtained by simple sample dilution.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30100 - Basic medicine

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2024

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Practical Laboratory Medicine

  • ISSN

    2352-5517

  • e-ISSN

    2352-5517

  • Svazek periodika

    39

  • Číslo periodika v rámci svazku

    March

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    8

  • Strana od-do

    e00359

  • Kód UT WoS článku

    001175273100001

  • EID výsledku v databázi Scopus

    2-s2.0-85183763540