2018
Recurrent aphthous stomatitis and gene variability in selected interleukins: a case-control study
BOŘILOVÁ LINHARTOVÁ, Petra, Július JÁNOŠ, Simona SLEZÁKOVÁ, Jirina BARTOVA, Jitka PETANOVA et. al.Základní údaje
Originální název
Recurrent aphthous stomatitis and gene variability in selected interleukins: a case-control study
Autoři
BOŘILOVÁ LINHARTOVÁ, Petra (203 Česká republika, domácí), Július JÁNOŠ (703 Slovensko, domácí), Simona SLEZÁKOVÁ (203 Česká republika, domácí), Jirina BARTOVA (203 Česká republika), Jitka PETANOVA (203 Česká republika), Pavel KUKLÍNEK (203 Česká republika, domácí), Antonín FASSMANN (203 Česká republika, domácí), Ladislav DUŠEK (203 Česká republika, domácí) a Lydie IZAKOVIČOVÁ HOLLÁ (203 Česká republika, garant, domácí)
Vydání
EUROPEAN JOURNAL OF ORAL SCIENCES, HOBOKEN, WILEY-BLACKWELL, 2018, 0909-8836
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30208 Dentistry, oral surgery and medicine
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.810
Kód RIV
RIV/00216224:14110/18:00101375
Organizační jednotka
Lékařská fakulta
UT WoS
000449881600006
Klíčová slova anglicky
association studies; candidate gene; genetic; immunity; oral ulcer; polymorphisms
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 2. 2019 18:59, Soňa Böhmová
Anotace
V originále
Genetic factors, especially those related to immune system functioning, have been intensively studied to determine their role in the development of recurrent aphthous stomatitis (RAS). The aim of the present study was to analyze gene variability in interleukin (IL)2, IL4 (and its receptor alpha, IL4R alpha), IL10, and IL13, which were selected based on literature review and/or their functional relevance, in Czech patients with RAS and in healthy controls. In total, 252 subjects (178 controls and 74 patients with RAS) were enrolled in this case-control study, and their detailed anamnestic, clinical, and laboratory data were obtained. Nine polymorphisms in the genes encoding interleukins were determined using PCR techniques. There were no significant differences in allele or genotype frequencies of the IL2, IL4, IL4R alpha, IL10, and IL13 polymorphisms rs2069762/rs2069763, rs2243250/rs79071878, rs1801275, rs1800896, and rs1800925, respectively, between controls and patients with RAS. The minority alleles rs1800871 and rs1800872, which encode variants of IL10, were associated with a statistically significantly higher risk of RAS, as confirmed by the results of genotype and haplotype analyses. We suggest that variability in the IL10 gene may play an important role in the development of RAS in the Czech population.
Návaznosti
GB14-37368G, projekt VaV |
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MUNI/A/1008/2017, interní kód MU |
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NV15-29336A, projekt VaV |
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ROZV/24/LF/2018, interní kód MU |
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