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干扰素γ诱导蛋白 16(IFI16)和黑色素瘤缺失 2(AIM2)基因中的变异可调节炎症反应,与牙周炎有关。

Variants in interferon gamma inducible protein 16 (IFI16) and absent in melanoma 2 (AIM2) genes that modulate inflammatory response are associated with periodontitis.

机构信息

Laboratório de Imunofarmacologia e Biologia Molecular, Departamento de Bioregulação, Instituto de Ciências da Saúde, Universidade Federal da Bahia-UFBA, Salvador, Bahia, Brazil; Escola de Saúde, Faculdade Adventista da Bahia-FADBA, Cachoeira, Bahia, Brazil.

Fundação Programa de Controle de Asma e Rinite Alérgica da Bahia, ProAR e Universidade Federal da Bahia, Salvador, Bahia, Brazil.

出版信息

Arch Oral Biol. 2023 Mar;147:105640. doi: 10.1016/j.archoralbio.2023.105640. Epub 2023 Feb 3.

Abstract

OBJECTIVE

Evaluate the association of genetic variants of the interferon gamma inducible protein 16 (IFI16) and absent in melanoma 2 (AIM2) genes with periodontitis.

METHODS

The study involved 117 individuals with periodontitis and 389 without periodontitis, all Brazilians, miscegenated. Individuals with periodontitis presented at least 4 teeth with ≥ 1 site with probing depth ≥ 4 mm; clinical attachment level ≥ 3 mm on the same site and bleeding upon stimulus. Genotyping was performed using the Infinium Multi-Ethnic AMR/AFR-8 Bead Chip focused on Hispanic and African American populations with approximately 2 million markers of the human genome. Multivariate logistic regression was performed to identify associations in additive, dominant and recessive models adjusted for covariates age, obesity, mouth breathing, flossing, asthma, and ancestry.

RESULTS

In IFI16, the rs75985579-A is positively associated with periodontitis in the additive (Odds Ratio adjusted (ORadjusted) 2.65, 95% confidence interval (CI):1.25-5.60, p value: 0.007) and dominant models (ORadjusted 2.56, 95%CI:1.13-5.81, p value: 0.017). In AIM2, the rs76457189-G, is associated negatively with periodontitis in two genetic models evaluated, additive (ORadjusted 0.21, 95%CI:0.05-0.94, p value: 0.022) and dominant (ORadjusted 0.21, 95%CI:0.05-0.94, p value: 0.022).

CONCLUSIONS

These results have shown that variants in the IFI16 and AIM2 genes are associated with periodontitis. Individuals with at least one A (adenine) allele of the rs75985579 (IFI16) are more than twice as likely to have periodontitis, while individuals with the G (guanine) allele of rs76457189 (AIM2) are less likely to be diagnosed with periodontitis, providing a negative association with periodontitis.

摘要

目的

评估干扰素γ诱导蛋白 16(IFI16)和黑色素瘤缺失 2(AIM2)基因的遗传变异与牙周炎的关联。

方法

本研究纳入了 117 名牙周炎患者和 389 名非牙周炎患者,所有参与者均为巴西混血人群。牙周炎患者至少有 4 颗牙齿在≥1 个位点上的探诊深度≥4mm,临床附着水平≥3mm,在同一部位有刺激后出血。基因分型使用 Infinium Multi-Ethnic AMR/AFR-8 Bead Chip 进行,该芯片针对西班牙裔和非裔美国人人群,包含约 200 万个人类基因组标记物。采用多元逻辑回归分析,在调整年龄、肥胖、口呼吸、用牙线洁牙、哮喘和祖源等混杂因素后,分别在加性、显性和隐性模型中识别关联。

结果

在 IFI16 基因中,rs75985579-A 等位基因在加性模型(调整后的比值比(ORadjusted)为 2.65,95%置信区间(CI):1.25-5.60,p 值:0.007)和显性模型(ORadjusted 为 2.56,95%CI:1.13-5.81,p 值:0.017)中与牙周炎呈正相关。在 AIM2 基因中,rs76457189-G 等位基因在两种评估的遗传模型中与牙周炎呈负相关,加性模型(ORadjusted 为 0.21,95%CI:0.05-0.94,p 值:0.022)和显性模型(ORadjusted 为 0.21,95%CI:0.05-0.94,p 值:0.022)。

结论

这些结果表明,IFI16 和 AIM2 基因的变异与牙周炎有关。rs75985579(IFI16)至少有一个 A(腺嘌呤)等位基因的个体发生牙周炎的风险增加两倍以上,而 rs76457189(AIM2)的 G(鸟嘌呤)等位基因的个体发生牙周炎的风险降低,与牙周炎呈负相关。

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