AIM2和Pycard基因多态性与牙周炎与冠心病易感性的关系

IF 1.5 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Clinical, Cosmetic and Investigational Dentistry Pub Date : 2023-11-22 eCollection Date: 2023-01-01 DOI:10.2147/CCIDE.S440577
Zina Ali Daily, Batool Hassan Al-Ghurabi, Ahmed Makki A Al-Qarakhli, Hashim Mueen Hussein
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引用次数: 0

摘要

背景:炎症小体成分的许多遗传变异与普通人群中的普遍疾病有关,包括牙周炎和心血管疾病。基因多态性在炎症性疾病的发生和发展中起着至关重要的作用。AIM2基因变异与炎症性疾病相关的研究有限,PYCARD基因变异与炎症性疾病相关的研究未见。目的:本病例对照研究AIM2和Pycard基因单核苷酸多态性与合并和不合并冠心病牙周炎易感性的关系,测定合并和不合并冠心病牙周炎患者唾液中白细胞介素-18和气凝胶蛋白D水平及其与唾液白细胞介素-18和气凝胶蛋白D水平及临床牙周参数的相关性。方法:本研究招募了120名受试者:30名健康受试者(对照组,C), 30名全身性牙周炎(P), 30名动脉粥样硬化冠心病伴临床健康牙周(AS-C), 30名动脉粥样硬化冠心病伴全身性牙周炎(AS-P)。记录所有个体的人口统计数据,收集唾液和血液样本,然后详细记录牙周特征。这些参数包括斑块指数、探针时出血、探针袋深度和临床附着丧失。采用聚合酶链反应、电泳和测序分析AIM2和Pycard基因多态性。采用酶联免疫吸附试验(ELISA)测定小鼠唾液中白细胞介素-18和气皮素D的水平。结果:研究结果为高频率(T)单核苷酸多态性。与对照组相比,牙周炎组、动脉粥样硬化冠心病伴健康牙周组织组和动脉粥样硬化冠心病伴全身性牙周炎组AIM2基因GT和TT基因型高,Pycard基因CT和TT基因型高。与健康对照组相比,三组患者唾液白细胞介素-18和气真皮蛋白D水平升高。这两种单核苷酸多态性也与唾液白细胞介素-18和气真皮蛋白D水平升高和牙周炎临床指标恶化显著相关。结论:AIM2和Pycard基因的单核苷酸多态性与伴有和/或不伴有冠心病的牙周炎风险增加相关。唾液白细胞介素-18和气真皮蛋白D水平升高与伴有和/或不伴有冠心病的牙周炎相关并有影响这些单核苷酸多态性可能为牙周炎伴或不伴动脉粥样硬化冠心病的发病机制中的遗传作用提供证据。
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Association Between AIM2 and Pycard Genes Polymorphisms and Susceptibility to Periodontitis with Coronary Heart Disease.

Background: Numerous genetic variations in inflammasome components are linked to prevalent disorders in the general population, including periodontitis and cardiovascular illness. Polymorphisms in the genes play a critical in the initiation and development of inflammatory diseases. The limited study on AIM2 gene variation associated with inflammatory disease and no study of PYCARD gene variation associated with inflammatory disease.

Objective: This case-control study was to examine the association between the single nucleotide polymorphism of AIM2 and Pycard genes with susceptibility to periodontitis with and without coronary heart disease, to determine interleuken-18 and gasdermin D levels in the saliva of periodontitis with and without coronary heart disease patients, as well as their correlation with salivary interleuken-18 and gasdermin D levels and clinical periodontal parameters.

Methods: The present study recruited 120 participants: 30 were healthy subjects (control, C), 30 had generalized periodontitis (P), 30 had atherosclerosis coronary heart disease with clinically healthy periodontium (AS-C), and 30 had atherosclerosis coronary heart disease with generalized periodontitis (AS-P). All individuals' demographic data recorded, saliva and blood samples collected, then periodontal characteristics were detailed. These parameters include plaque index, bleeding on probing, probing pocket depth, and clinical attachment loss. AIM2 and Pycard gene polymorphisms were analyzed by polymerase chain reaction assay, electrophoresis and sequencing. An enzyme-linked immunosorbent assay (ELISA) was conducted to determine the level of interleuken-18 and gasdermin D in their saliva.

Results: The study result of high frequency (T) in single-nucleotide polymorphisms. The high genotypes distribution of GT and TT genotypes in the AIM2 gene and the CT and TT genotypes in the Pycard gene were detected in the periodontitis, atherosclerosis coronary heart disease with healthy periodontium and atherosclerosis coronary heart disease with generalized periodontitis groups as compared to control group. Elevation of salivary interleuken-18 and gasdermin D levels in three patients' groups compared to healthy controls. Both these single-nucleotide polymorphisms also significantly correlated with higher salivary interleuken-18 and gasdermin D levels and worse clinical indices of periodontitis.

Conclusion: Single-nucleotide polymorphisms in the AIM2 and Pycard genes are associated with an increased risk of developing periodontitis with and/or without coronary heart disease. Elevation of salivary interleuken-18 and gasdermin D levels associated and impacted on periodontitis with and/or without coronary heart disease. These single-nucleotide polymorphisms may provide evidence for a genetic role in the pathogenesis of periodontitis with and without atherosclerosis coronary heart disease.

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来源期刊
CiteScore
3.90
自引率
5.60%
发文量
43
审稿时长
16 weeks
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