ŠUMOVÁ, Barbora, Lucie Andrés CEREZO, Lenka SZCZUKOVÁ, Lucie NEKVINDOVÁ, Michal UHER, Hana HULEJOVÁ, Radka MORAVCOVÁ, Mariam GRIGORIAN, Karel PAVELKA, Jiří VENCOVSKÝ, Ladislav ŠENOLT a Jakub ZÁVADA. Circulating S100 proteins effectively discriminate SLE patients from healthy controls: a cross-sectional study. Rheumatology International. Heidelberg: Springer, 2019, roč. 39, č. 3, s. 469-478. ISSN 0172-8172. Dostupné z: https://dx.doi.org/10.1007/s00296-018-4190-2.
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Základní údaje
Originální název Circulating S100 proteins effectively discriminate SLE patients from healthy controls: a cross-sectional study
Autoři ŠUMOVÁ, Barbora (203 Česká republika), Lucie Andrés CEREZO (203 Česká republika), Lenka SZCZUKOVÁ (203 Česká republika, domácí), Lucie NEKVINDOVÁ (203 Česká republika, domácí), Michal UHER (203 Česká republika, domácí), Hana HULEJOVÁ (203 Česká republika), Radka MORAVCOVÁ (203 Česká republika), Mariam GRIGORIAN (208 Dánsko), Karel PAVELKA (203 Česká republika), Jiří VENCOVSKÝ (203 Česká republika), Ladislav ŠENOLT (203 Česká republika) a Jakub ZÁVADA (203 Česká republika, garant).
Vydání Rheumatology International, Heidelberg, Springer, 2019, 0172-8172.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30226 Rheumatology
Stát vydavatele Německo
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 1.984
Kód RIV RIV/00216224:14110/19:00109000
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1007/s00296-018-4190-2
UT WoS 000458566100007
Klíčová slova anglicky Biomarkers; SLE; S100 proteins; Disease activity
Štítky 14119612, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 15. 4. 2019 14:50.
Anotace
S100 proteins are currently being investigated as potential diagnostic and prognostic biomarkers of several cancers and inflammatory diseases. The aims of this study were to analyse the plasma levels of S100A4, S100A8/9 and S100A12 in patients with incomplete systemic lupus erythematosus (iSLE), in patients with established SLE and in healthy controls (HCs) and to investigate the potential utility of the S100 proteins as diagnostic or activity-specific biomarkers in SLE. Plasma levels were measured by ELISA in a cross-sectional cohort study of 44 patients with SLE, 8 patients with iSLE and 43 HCs. Disease activity was assessed using the SLEDAI-2K. The mean levels of all S100 proteins were significantly higher in SLE patients compared to HCs. In iSLE patients, the levels of S100A4 and S100A12 but not S100A8/9 were also significantly higher compared to HCs. There were no significant differences in S100 levels between the iSLE and SLE patients. Plasma S100 proteins levels effectively discriminated between SLE patients and HCs. The area under the curve (AUC) for S100A4, S100A8/9 and S100A12 plasma levels was 0.989 (95% CI 0.976-1.000), 0.678 (95% CI 0.563-0.792) and 0.807 (95% CI 0.715-0.899), respectively. S100 levels did not differentiate between patients with high and low disease activity. Only the S100A12 levels were significantly associated with SLEDAI-2K and with cSLEDAI-2K. S100 proteins were significantly higher in SLE patients compared HCs and particularly S100A4 could be proposed as a potential diagnostic biomarker for SLE.
VytisknoutZobrazeno: 16. 7. 2024 20:30