Detailed Information on Publication Record
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.Basic information
Original name
Recurrent aphthous stomatitis and gene variability in selected interleukins: a case-control study
Authors
BOŘILOVÁ LINHARTOVÁ, Petra (203 Czech Republic, belonging to the institution), Július JÁNOŠ (703 Slovakia, belonging to the institution), Simona SLEZÁKOVÁ (203 Czech Republic, belonging to the institution), Jirina BARTOVA (203 Czech Republic), Jitka PETANOVA (203 Czech Republic), Pavel KUKLÍNEK (203 Czech Republic, belonging to the institution), Antonín FASSMANN (203 Czech Republic, belonging to the institution), Ladislav DUŠEK (203 Czech Republic, belonging to the institution) and Lydie IZAKOVIČOVÁ HOLLÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
EUROPEAN JOURNAL OF ORAL SCIENCES, HOBOKEN, WILEY-BLACKWELL, 2018, 0909-8836
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30208 Dentistry, oral surgery and medicine
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 1.810
RIV identification code
RIV/00216224:14110/18:00101375
Organization unit
Faculty of Medicine
UT WoS
000449881600006
Keywords in English
association studies; candidate gene; genetic; immunity; oral ulcer; polymorphisms
Tags
International impact, Reviewed
Změněno: 10/2/2019 18:59, Soňa Böhmová
Abstract
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.
Links
GB14-37368G, research and development project |
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MUNI/A/1008/2017, interní kód MU |
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NV15-29336A, research and development project |
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ROZV/24/LF/2018, interní kód MU |
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