牙周炎
背景(考古学)
免疫系统
免疫学
医学
炎症
孟德尔随机化
全基因组关联研究
二、侵袭性牙周炎
生物
生物信息学
基因
内科学
基因型
遗传学
遗传变异
单核苷酸多态性
古生物学
作者
Xinjian Ye,Yijing Bai,Mengjun Li,Yuhang Ye,Yitong Chen,Bin Liu,Yuwei Dai,Shan Wang,Weiyi Pan,Zhiyong Wang,Yingying Mao,Qianming Chen
出处
期刊:eLife
[eLife Sciences Publications Ltd]
日期:2023-11-23
卷期号:12
被引量:7
摘要
Periodontitis drives irreversible destruction of periodontal tissue and is prone to exacerbating inflammatory disorders. Systemic immunomodulatory management continues to be an attractive approach in periodontal care, particularly within the context of ‘predictive, preventive, and personalized’ periodontics. The present study incorporated genetic proxies identified through genome-wide association studies for circulating immune cells and periodontitis into a comprehensive Mendelian randomization (MR) framework. Univariable MR, multivariable MR, subgroup analysis, reverse MR, and Bayesian model averaging (MR-BMA) were utilized to investigate the causal relationships. Furthermore, transcriptome-wide association study and colocalization analysis were deployed to pinpoint the underlying genes. Consequently, the MR study indicated a causal association between circulating neutrophils, natural killer T cells, plasmacytoid dendritic cells, and an elevated risk of periodontitis. MR-BMA analysis revealed that neutrophils were the primary contributors to periodontitis. The high-confidence genes S100A9 and S100A12 , located on 1q21.3, could potentially serve as immunomodulatory targets for neutrophil-mediated periodontitis. These findings hold promise for early diagnosis, risk assessment, targeted prevention, and personalized treatment of periodontitis. Considering the marginal association observed in our study, further research is required to comprehend the biological underpinnings and ascertain the clinical relevance thoroughly.
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