2017
Association of interleukin-8 gene variability with recurrent aphthous stomatitis
SLEZÁKOVÁ, Simona, Petra BOŘILOVÁ LINHARTOVÁ, Denisa KAVŘÍKOVÁ, Jiřina BÁRTOVÁ, Jitka PETANOVÁ et. al.Základní údaje
Originální název
Association of interleukin-8 gene variability with recurrent aphthous stomatitis
Autoři
SLEZÁKOVÁ, Simona (203 Česká republika, domácí), Petra BOŘILOVÁ LINHARTOVÁ (203 Česká republika, domácí), Denisa KAVŘÍKOVÁ (203 Česká republika, domácí), Jiřina BÁRTOVÁ (203 Česká republika), Jitka PETANOVÁ (203 Česká republika), Pavel KUKLÍNEK (203 Česká republika, domácí), Antonín FASSMANN (203 Česká republika, domácí) a Lydie IZAKOVIČOVÁ HOLLÁ (203 Česká republika, garant, domácí)
Vydání
The Biomania Student Scientific Meeting 2017, Brno, 2017
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30208 Dentistry, oral surgery and medicine
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/17:00100727
Organizační jednotka
Lékařská fakulta
ISBN
978-80-210-8737-8
Klíčová slova anglicky
interleukin-8; association studies; polymorphism; recurrent aphthous stomatitis
Změněno: 18. 1. 2019 14:12, Mgr. et Mgr. Simona Slezáková, Ph.D.
Anotace
V originále
Objectives: Variability in the interleukin-8 gene (IL-8), encoding a proinflammatory chemokine, was recently associated with Behçet's syndrome, disease with recurrent oral ulcers as one of its symptoms. The aim of this study was to analyse four single nucleotide polymorphisms (SNPs) in IL-8 and its receptor 2 (CXCR2) in patients with recurrent aphthous stomatitis (RAS) and healthy controls. Methods: Totally, 238 subjects were enrolled in this case-control study: 64 patients with RAS and 174 healthy controls were genotyped for SNPs in IL-8 (-251A/T, +396T/G, +781C/T) and CXCR2 (+1208C/T) by a method based on PCR using 5´ nuclease TaqMan assays. Results: The allele and genotype frequencies of studied polymorphisms between RAS patients and healthy controls were similar, with the exception of statistically significant differences in IL-8 +781 TT vs. CC+CT genotype frequencies between both groups. However, IL-8 A(-251)/G(+396)/C(+781) haplotype was significantly more frequent in patients with RAS (P<0.02; OR=4.2; 95% CI=1.3-13.8) than in healthy controls. Conclusions: Our study indicates that the IL-8 gene variability may affect susceptibility to RAS in the Czech population.
Návaznosti
GB14-37368G, projekt VaV |
| ||
MUNI/A/0948/2016, interní kód MU |
| ||
NV15-29336A, projekt VaV |
|