2010
Crohn's disease activity versus extent of DNA damage/repair and variability in the RAGE gene
PÁCAL, Lukáš, Jana VARVAŘOVSKÁ, Josef SÝKORA, Jana KOŽELUHOVÁ, Zdeněk RUŠAVÝ et. al.Základní údaje
Originální název
Crohn's disease activity versus extent of DNA damage/repair and variability in the RAGE gene
Autoři
PÁCAL, Lukáš (203 Česká republika, garant), Jana VARVAŘOVSKÁ (203 Česká republika), Josef SÝKORA (203 Česká republika), Jana KOŽELUHOVÁ (203 Česká republika), Zdeněk RUŠAVÝ (203 Česká republika), Jaroslav RACEK (203 Česká republika), Rudolf ŠTĚTINA (203 Česká republika) a Kateřina KAŇKOVÁ (203 Česká republika)
Vydání
Scripta Medica, Brno, Masaryk University, Faculty of Medicine, 2010, 1211-3395
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/10:00040533
Organizační jednotka
Lékařská fakulta
Klíčová slova česky
AGEs; Crohn; glykoxidace; nutrigenetika; RAGE
Klíčová slova anglicky
AGEs; Crohn; glycoxidation; nutrigenetics; RAGE
Změněno: 23. 8. 2010 12:16, prof. MUDr. Kateřina Kaňková, Ph.D.
Anotace
V originále
The aim of the study was to investigate relationships between the extent of oxidative stress and DNA damage/repair, disease severity and selected genetic variants in the RAGE gene in Crohns disease (CD) patients. Study comprised a total of 46 subjects with CD and 99 control subjects. Disease activity was characterised by Crohn Disease Activity Index (CDAI) and pediatric CDAI (PCDAI) and complications requiring surgery (abscess, fistula or stenosis). Selected markers of oxidative stress (superoxide dismutase (Ery-SOD), glutathione peroxidise (WB-GPx), total plasma antioxidant capacity (P-tAOC), reduced glutathione (Ery-GSH) and malondialdehyde (P-MDA)), DNA damage (DNA single strand breaks) and repair capacity detected (DNArc) by Comet assay were ascertained. Four SNPs in the RAGE gene were detected by PCR. Significant correlation between CD duration and DNArc was identified in adult patients (r = 0.44, P = 0.039) and adult CD subjects had significantly higher Ery-SOD levels (P = 0.0005). In children, both CDAI and PCDAI significantly correlated with P-tAOC (r = -0.5, P = 0.02 and r = -0.53, P = 0.013, respectively) and also with WB-GPx (r = -0.5, P = 0.03 and r = -0.51, P = 0.018, respectively). Children CD patients also exhibited significant correlation between age and Ery-GSH and P-MDA (r = -0.6, P = 0.005 and r = 0.5, P = 0.02, respectively). Significant differences in Ery-GSH and P-MDA were found between CD patients with and without history of complications (P = 0.05 and P = 0.013, respectively). There was no statistically significant relationship between the carrier state of any of the four RAGE SNPs and ox. stress, DNA damage or DNA repair parameters analysed. In conclusion, intestinal inflammation is reflected in selected circulating markers of oxidative and genotoxic stress.
Návaznosti
KJB501620601, projekt VaV |
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