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复发性阿弗他口炎与特定白细胞介素的基因变异性:一项病例对照研究。

Recurrent aphthous stomatitis and gene variability in selected interleukins: a case-control study.

作者信息

Borilova Linhartova Petra, Janos Julius, Slezakova Simona, Bartova Jirina, Petanova Jitka, Kuklinek Pavel, Fassmann Antonin, Dusek Ladislav, Izakovicova Holla Lydie

机构信息

Clinic of Stomatology, Institution Shared with St. Anne's Faculty Hospital, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Department of Pathophysiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

出版信息

Eur J Oral Sci. 2018 Dec;126(6):485-492. doi: 10.1111/eos.12577. Epub 2018 Oct 20.

Abstract

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 α, IL4Rα), 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, IL4Rα, 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.

摘要

遗传因素,尤其是那些与免疫系统功能相关的因素,已被深入研究以确定它们在复发性阿弗他口炎(RAS)发病中的作用。本研究的目的是分析白细胞介素(IL)2、IL4(及其受体α,IL4Rα)、IL10和IL13的基因变异性,这些基因是根据文献综述和/或其功能相关性在捷克RAS患者和健康对照中选择的。总共252名受试者(178名对照和74名RAS患者)参与了这项病例对照研究,并获得了他们详细的既往史、临床和实验室数据。使用PCR技术确定了编码白细胞介素的基因中的9种多态性。在RAS患者和对照之间,IL2、IL4、IL4Rα、IL10和IL13多态性rs2069762/rs2069763、rs2243250/rs79071878、rs1801275、rs1800896和rs1800925的等位基因或基因型频率分别没有显著差异。编码IL10变体的少数等位基因rs1800871和rs1800872与RAS的统计学显著较高风险相关,基因型和单倍型分析结果证实了这一点。我们认为IL10基因的变异性可能在捷克人群RAS的发病中起重要作用。

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