Dhungana Gunaraj, Srisai Dollada, Sampath Chethan, Soliman Jeremiah, Kelly Regan M, Saleh Honar Y, Sedik Abdelrahman, Raynes Edilberto, Ferguson Alexys, Alluri Leela Subhashini Choudary, Gangula Pandu R
Department of Oral Diagnostic Sciences & Research, School of Dentistry, Meharry Medical College, Nashville, TN 37208, USA.
Department of Professional and Medical Education, School of Medicine, Meharry Medical College, Nashville, TN 37208, USA.
Dent J (Basel). 2025 Feb 25;13(3):98. doi: 10.3390/dj13030098.
Periodontal disease (PD) is a chronic inflammatory condition caused by dysbiosis of the oral microbiome. PD is linked to systemic inflammation and endothelial dysfunction, which associate it with cardiovascular disease (CVD). This systematic review explores the molecular and microbial mechanisms through which periodontal pathogens, including "Red Complex" bacteria (, , ) and , influence cardiovascular health via inflammatory pathways, immune modulation, and microbial dissemination. : A systematic review was conducted following PRISMA guidelines. A literature search was conducted in the PubMed and ScienceDirect databases using relevant keywords, with strict inclusion and exclusion criteria, from the first week of September 2024 to the first week of October 2024. Studies addressing the relationship between PD and CVD were assessed for methodological rigor, relevance, and data availability. The outcomes were synthesized using a descriptive narrative approach. Out of 591 records screened, 421 full-text articles were sought for retrieval. The final review included 58 articles providing supplementary aggregated data after eligibility assessment. The pathogenesis of PD involves the activation of immune cells and the release of pro-inflammatory cytokines (such as IL-1, IL-6, TNF-α, and PGE2) and chemokines (including IL-8 and MCP-1) along with oxidative stress driven by reactive oxygen species (ROS). Periodontal pathogens trigger endothelial oxidative stress and systemic inflammation via Toll-like receptors (TLRs), NF-κB signaling, and nitric oxide (NO) dysregulation, contributing to endothelial dysfunction and atherogenesis. Biomarkers, such as C-reactive protein, interleukins, and matrix metalloproteinases (MMPs), further highlight the systemic inflammatory response. This review underscores the significant role of periodontal pathogens and inflammatory mediators in systemic health, particularly in the progression of CVD. Although existing evidence illustrates these associations, the underlying molecular mechanisms remain inadequately understood, indicating a need for further research to advance precision medicine and therapeutic strategies.
牙周病(PD)是一种由口腔微生物群失调引起的慢性炎症性疾病。PD与全身炎症和内皮功能障碍有关,这使其与心血管疾病(CVD)相关联。本系统评价探讨了包括“红色复合体”细菌(牙龈卟啉单胞菌、福赛坦氏菌、齿垢密螺旋体)和伴放线聚集杆菌在内的牙周病原体通过炎症途径、免疫调节和微生物传播影响心血管健康的分子和微生物机制。方法:按照PRISMA指南进行系统评价。于2024年9月的第一周 至2024年10月的第一周,在PubMed和ScienceDirect数据库中使用相关关键词进行文献检索,并制定严格的纳入和排除标准。对涉及PD与CVD关系的研究进行方法学严谨性、相关性和数据可用性评估。采用描述性叙述方法对结果进行综合分析。在筛选的591条记录中,检索了421篇全文文章。最终评价纳入了58篇文章,这些文章在资格评估后提供了补充汇总数据。PD的发病机制涉及免疫细胞的激活、促炎细胞因子(如IL-1、IL-6、TNF-α和PGE2)和趋化因子(包括IL-8和MCP-1)的释放,以及活性氧(ROS)驱动的氧化应激。牙周病原体通过Toll样受体(TLRs)、NF-κB信号传导和一氧化氮(NO)失调引发内皮氧化应激和全身炎症,导致内皮功能障碍和动脉粥样硬化的发生。生物标志物,如C反应蛋白、白细胞介素和基质金属蛋白酶(MMPs),进一步突出了全身炎症反应。本综述强调了牙周病原体和炎症介质在全身健康中的重要作用,特别是在CVD进展中的作用。尽管现有证据表明了这些关联,但其潜在的分子机制仍未得到充分理解,这表明需要进一步研究以推进精准医学和治疗策略。