Suppr超能文献

巴西人群良性游走性舌炎中功能基因多态性的研究:白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α

Investigation of functional gene polymorphisms: IL-1B, IL-6 and TNFA in benign migratory glossitis in Brazilian individuals.

作者信息

Guimarães André Luiz Sena, Correia-Silva Jeane de Fátima, Diniz Marina Gonçalves, Xavier Guilherme Machado, Horta Martinho Campolina Rebello, Gomez Ricardo Santiago

机构信息

Department of Dentistry, Universidade Estadual de Montes Claros, Minas Gerais, Brazil.

出版信息

J Oral Pathol Med. 2007 Oct;36(9):533-7. doi: 10.1111/j.1600-0714.2007.00559.x.

Abstract

BACKGROUND

Benign migratory glossitis (BMG) is a very common immunological oral disease of unknown aetiology.

METHODS AND SUBJECTS

Fifty-three consecutive subjects affected by BMG and 53 age- and sex-matched control subjects were genotyped for IL-1B, IL-6 and TNFA polymorphisms. Binary logistic regression models were fitted and values of P < 0.05 were considered significant.

RESULTS

A significant difference in the distribution of IL-1B genotypes was observed in the group with BMG in univariate analyses (P = 0.01). The multivariate analyses showed that the CT genotype of the IL1-B gene was significantly associated with a high risk to develop BMG (P = 0.02, OR 2.76). The combined presence of IL-1beta high and intermediate producers genotypes was also associated with BMG in multivariate analyses (P = 0.01, OR 3.05). IL-6 and TNFA polymorphisms were not associated with BMG in the univariate and multivariate analyses.

CONCLUSION

Our findings demonstrate that the polymorphism +3954 IL-1B is associated with an increased risk of BMG development and suggest a genetic basis for disease development.

摘要

背景

良性游走性舌炎(BMG)是一种病因不明的非常常见的免疫性口腔疾病。

方法与对象

对53例连续的BMG患者和53例年龄及性别匹配的对照对象进行白细胞介素-1β(IL-1B)、白细胞介素-6(IL-6)和肿瘤坏死因子α(TNFA)基因多态性基因分型。采用二元逻辑回归模型进行分析,P < 0.05的值被认为具有统计学意义。

结果

单因素分析显示,BMG组IL-1B基因型分布存在显著差异(P = 0.01)。多因素分析表明,IL1-B基因的CT基因型与发生BMG的高风险显著相关(P = 0.02,比值比2.76)。多因素分析还显示,白细胞介素-1β高表达和中等表达基因型的联合存在也与BMG相关(P = 0.01,比值比3.05)。单因素和多因素分析中,IL-6和TNFA基因多态性与BMG均无关联。

结论

我们的研究结果表明,IL-1B基因+3954位点的多态性与BMG发生风险增加相关,并提示了该疾病发生的遗传基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验