School & Hospital of Stomatology, Wenzhou Medical University, Wenzhou, China.
The 1 School of Medicine, School of Information and Engineering, The 1 Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Front Cell Infect Microbiol. 2024 May 15;14:1380209. doi: 10.3389/fcimb.2024.1380209. eCollection 2024.
The oral cavity and gut tract, being interconnected and rich in microbiota, may have a shared influence on gingivitis. However, the specific role of distinct gut microbiota taxa in gingivitis remains unexplored. Utilizing Mendelian Randomization (MR) as an ideal method for causal inference avoiding reverse causality and potential confounding factors, we conducted a comprehensive two-sample MR study to uncover the potential genetic causal impact of gut microbiota on gingivitis.
Instrumental variables were chosen from single nucleotide polymorphisms (SNPs) strongly associated with 418 gut microbiota taxa, involving 14,306 individuals. Gingivitis, with 4,120 cases and 195,395 controls, served as the outcome. Causal effects were assessed using random-effect inverse variance-weighted, weighted median, and MR-Egger methods. For replication and meta-analysis, gingivitis data from IEU OpenGWAS were employed. Sensitivity analyses included Cochran's Q tests, funnel plots, leave-one-out analyses, and MR-Egger intercept tests. This study aimed to assess the genetic correlation between the genetically predicted gut microbiota and gingivitis using linkage disequilibrium score regression (LDSC).
Three gut microbiota taxa (class Actinobacteria id.419, family Defluviitaleaceae id.1924, genus Defluviitaleaceae UCG011 id.11287) are predicted to causally contribute to an increased risk of gingivitis (P< 0.05). Additionally, four gut microbiota taxa (class Actinobacteria id.419, genus Escherichia Shigella id.3504, genus Ruminococcaceae UCG002 id.11360) potentially exhibit inhibitory causal effects on the risk of gingivitis (P< 0.05). No significant evidence of heterogeneity or pleiotropy is detected. Our findings indicate a suggestive genetic correlation between class Actinobacteria id.419, class Bacteroidia id.912, family Defluviitaleaceae id.1924, genus Escherichia Shigella id.3504 and gingivitis.
Our study establishes the genetic causal effect of 418 gut microbiota taxa on gingivitis, offering insights for clinical interventions targeting gingivitis. Subsequent research endeavors are essential to corroborate the findings of our present study.
口腔和肠道相互连通,且富含微生物群,这可能对牙龈炎有共同的影响。然而,不同的肠道微生物群分类在牙龈炎中的具体作用仍未得到探索。利用孟德尔随机化(MR)作为一种避免反向因果关系和潜在混杂因素的理想因果推断方法,我们进行了一项全面的两样本 MR 研究,以揭示肠道微生物群对牙龈炎的潜在遗传因果影响。
我们从与 418 种肠道微生物群分类物强烈相关的单核苷酸多态性(SNP)中选择工具变量,涉及 14306 个人。牙龈炎作为结果,有 4120 例病例和 195395 例对照。使用随机效应逆方差加权、加权中位数和 MR-Egger 方法评估因果效应。为了复制和荟萃分析,我们使用了 IEU OpenGWAS 的牙龈炎数据。敏感性分析包括 Cochrane's Q 检验、漏斗图、逐一剔除分析和 MR-Egger 截距检验。本研究旨在使用连锁不平衡得分回归(LDSC)评估遗传预测的肠道微生物群与牙龈炎之间的遗传相关性。
有 3 种肠道微生物群分类物(类放线菌 id.419、科 Defluviitaleaceae id.1924、属 Defluviitaleaceae UCG011 id.11287)被预测为导致牙龈炎风险增加的原因(P<0.05)。此外,有 4 种肠道微生物群分类物(类放线菌 id.419、属 Escherichia Shigella id.3504、属 Ruminococcaceae UCG002 id.11360)可能对牙龈炎风险有抑制性的因果作用(P<0.05)。未检测到异质性或多效性的显著证据。我们的研究结果表明,类放线菌 id.419、类 Bacteroidia id.912、科 Defluviitaleaceae id.1924、属 Escherichia Shigella id.3504 与牙龈炎之间存在遗传相关性。
我们的研究确定了 418 种肠道微生物群分类物对牙龈炎的遗传因果作用,为针对牙龈炎的临床干预提供了新的见解。后续的研究工作对于证实我们目前研究的结果是必要的。