Dias Larissa Nadine da Silva, Coêlho Marina de Castro, Persuhn Darlene Camati, Ribeiro Isabella Lima Arrais, Freire Eutilia Andrade Medeiros, Oliveira Naila Francis Paulo de, Aquino Sabrina Garcia de
Universidade Federal da Paraíba - UFPB, Centro de Ciências da Saúde, Programa de Pós Graduação em Odontologia, João Pessoa, PB, Brasil.
Universidade Federal da Paraíba - UFPB, Centro de Ciências Exatas e da Natureza, Departamento de Biologia Molecular, João Pessoa, PB, Brasil.
J Appl Oral Sci. 2022 Apr 29;30:e20210567. doi: 10.1590/1678-7757-2021-0567. eCollection 2022.
The association between Periodontitis and Systemic Lupus Erythematosus (SLE) has been primarily based on their similar pathophysiology and both are associated with genetic polymorphisms.
To investigate an association between the methylation-related gene polymorphisms DNMT3B (rs2424913) and MTHFR (rs1801133) to Systemic Lupus Erythematosus (SLE) and Periodontitis.
In total, 196 individuals of all genders aged 24 to 60 years old were allocated into four groups based on their systemic and periodontal status, namely: Healthy control (n=60), periodontitis (n=51), SLE (n=47), and SLE + periodontitis (n=38). Individuals with SLE were stratified according to disease activity (SLEDAI) in inactive or active. We performed polymorphism analysis using PCR-RFLP with genomic DNA from mouthwash. We analyzed data using Fisher's Exact, Chi-square test, and regression models.
Periodontal status were similar in subjects with periodontitis alone and combined with SLE. SLE patients with periodontitis had a longer SLE diagnosis than SLE only (p=0.001). For DNMT3 B polymorphism, the periodontitis, SLE, and Inactive SLE + periodontitis groups showed a higher frequency of T allele and TT genotypes compared to healthy controls (p<0.05). Regression analyses showed that the TT genotype is a strong risk factor for periodontitis (OR=4.53; CI95%=1.13-18.05) and also for SLE without periodontitis (OR=11.57; CI95%=3.12-42.84) and SLE with periodontitis (OR=5.27; CI95%=1.25-22.11) when compared to control.
SLE patients with periodontitis had a longer length of SLE diagnosis. The DNMT3B (rs2424913) polymorphism was associated with periodontitis and SLE alone or combined with periodontitis. Our study contributes to understanding the genetic mechanisms involved in periodontitis and SLE susceptibility.
牙周炎与系统性红斑狼疮(SLE)之间的关联主要基于它们相似的病理生理学,且两者都与基因多态性有关。
研究甲基化相关基因多态性DNMT3B(rs2424913)和MTHFR(rs1801133)与系统性红斑狼疮(SLE)和牙周炎之间的关联。
总共196名年龄在24至60岁的各性别个体根据其全身和牙周状况被分为四组,即:健康对照组(n = 60)、牙周炎组(n = 51)、SLE组(n = 47)和SLE + 牙周炎组(n = 38)。SLE患者根据疾病活动度(SLEDAI)分为非活动或活动状态。我们使用PCR-RFLP对漱口水的基因组DNA进行多态性分析。我们使用Fisher精确检验、卡方检验和回归模型分析数据。
仅患有牙周炎的受试者和合并SLE的受试者的牙周状况相似。患有牙周炎的SLE患者的SLE诊断时间比仅患有SLE的患者更长(p = 0.001)。对于DNMT3B多态性,与健康对照组相比,牙周炎组、SLE组和非活动SLE + 牙周炎组的T等位基因和TT基因型频率更高(p < 0.05)。回归分析表明,与对照组相比,TT基因型是牙周炎(OR = 4.53;CI95% = 1.13 - 18.05)以及无牙周炎的SLE(OR = 11.57;CI95% = 3.12 - 42.84)和伴有牙周炎的SLE(OR = 5.27;CI95% = 1.25 - 22.11)的强风险因素。
患有牙周炎的SLE患者的SLE诊断时间更长。DNMT3B(rs2424913)多态性与牙周炎以及单独的SLE或合并牙周炎的SLE有关。我们的研究有助于理解参与牙周炎和SLE易感性的遗传机制。