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 < 0.0001) and 0.895 (0.9607) for SDMA (p < 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 < 0.0001) and 0.895 (0.9607) for SDMA (p < 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