Lin Jichao, Xu Qingjiang, Bi Wei, Yu Youcheng, Wang Qinglian
Department of Stomatology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, 361000, China.
Department of Stomatology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
BMC Oral Health. 2025 Jul 28;25(1):1270. doi: 10.1186/s12903-025-06658-z.
The disruption of microbiota balance could be a pivotal factor in the complications arising from periodontal disease-induced inflammation outside the mouth. Nonetheless, it remains uncertain whether there is a direct causal relationship between the oral and gut microbiomes and gingivitis, especially in distinguishing between acute and chronic gingivitis.
We performed a two-sample Mendelian randomization (MR) analysis using GWAS summary statistics from FinnGen data (149 acute gingivitis cases, 850 chronic gingivitis cases, and 195,395 controls) to explore the causal role of oral and gut microbiota. The primary analysis employed the inverse-variance weighted (IVW) method, augmented by four supplementary approaches: weighted median, weighted mode, and MR Egger regression, all aimed at detecting and adjusting for horizontal pleiotropy.
In the gut microbiota, the results of IVW showed that class Negativicutes, Verrucomicrobiae, genus Butyricicoccus, Eubacterium, Lactobacillus, order Selenomonadales and Verrucomicrobiales were linked to a higher risk of acute gingivitis, while family Peptostreptococcaceae, genus Coprococcus2, and genus Lachnospiraceae UCG001 were linked to a lower risk of acute gingivitis (P < 0.05). Class Erysipelotrichia, Methanobacteria, Verrucomicrobiae, family Defluviitaleaceae, Erysipelotrichaceae, Methanobacteriaceae, Verrucomicrobiaceae, genus Akkermansia, Christensenellaceae R 7group, Defluviitaleaceae UCG011, Methanobrevibacter, genus Paraprevotella, Senegalimassilia, order Erysipelotrichales, Methanobacteriales, Verrucomicrobiales, and phylum Cyanobacteria were linked to a higher risk of chronic gingivitis, while family Clostridiales vadin BB60 group, genus Allisonella, Dorea, and Lachnospiraceae UCG004 were linked to a lower risk of chronic gingivitis (P < 0.05). And in the oral microbiota, unknown Porphyromonas species (ASV0008) and Genus Porphyromonas were linked to higher risk of acute gingivitis (P < 0.05). Unknown Neisseria species (ASV0004) and unknown Veillonella species (ASV0001) were linked to higher risk of chronic gingivitis, while Class Bacilli was linked to lower risk of chronic gingivitis (P < 0.05).
This MR analysis confirms the distinct causal relationships between microbiota and both acute and chronic gingivitis, providing insights into potential prevention strategies in European.
Not applicable.
微生物群平衡的破坏可能是口腔外牙周病诱导炎症引发并发症的关键因素。然而,口腔和肠道微生物群与牙龈炎之间是否存在直接因果关系仍不确定,尤其是在区分急性和慢性牙龈炎方面。
我们使用来自芬兰基因数据的全基因组关联研究(GWAS)汇总统计数据(149例急性牙龈炎病例、850例慢性牙龈炎病例和195395例对照)进行了两样本孟德尔随机化(MR)分析,以探讨口腔和肠道微生物群的因果作用。主要分析采用逆方差加权(IVW)方法,并辅以四种补充方法:加权中位数、加权众数和MR Egger回归,所有这些方法都旨在检测和调整水平多效性。
在肠道微生物群中,IVW结果显示,Negativicutes纲、疣微菌门、丁酸球菌属、真杆菌属、乳杆菌属、月形单胞菌目和疣微菌目与急性牙龈炎风险较高相关,而消化链球菌科、粪球菌属2和毛螺菌科UCG001属与急性牙龈炎风险较低相关(P<0.05)。丹毒丝菌纲、甲烷杆菌纲、疣微菌门、脱铁杆菌科、丹毒丝菌科、甲烷杆菌科、疣微菌科、阿克曼氏菌属、克里斯滕森菌科R7组、脱铁杆菌科UCG011、甲烷短杆菌属、副普雷沃菌属、塞内加尔菌属、丹毒丝菌目、甲烷杆菌目、疣微菌目和蓝藻门与慢性牙龈炎风险较高相关,而梭菌目vadin BB60组、Allisonella属、多雷亚属和毛螺菌科UCG004属与慢性牙龈炎风险较低相关(P<0.05)。在口腔微生物群中,未知卟啉单胞菌属物种(ASV0008)和卟啉单胞菌属与急性牙龈炎风险较高相关(P<0.05)。未知奈瑟菌属物种(ASV0004)和未知韦荣球菌属物种(ASV0001)与慢性牙龈炎风险较高相关,而芽孢杆菌纲与慢性牙龈炎风险较低相关(P<0.05)。
这项MR分析证实了微生物群与急性和慢性牙龈炎之间存在明显的因果关系,为欧洲潜在预防策略提供了见解。
不适用。