Cen Lilan, Qin Ling, Chen Wanling, Wei Lihua, Tang Caixia, Teng Xiang, Tian Zhe
1Guangxi Academy of Medical Sciences, Department of Infectious Disease, the People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
2Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Pol J Microbiol. 2025 Jun 18;74(2):153-164. doi: 10.33073/pjm-2025-013. eCollection 2025 Jun 1.
Previous research has demonstrated a connection between an unbalanced gut microbiome (GM) and lung diseases, suggesting that gut bacteria may affect lung health through the "gut-lung" axis. However, the direct connection between GM and pulmonary embolism (PE) is unclear. Mendelian randomization studies were used to investigate GM's genetic relationship with PE. A total of 18,340 independent genewide association studies (GWAS) yielded single nucleotide polymorphisms (SNPs) linked to the GM, which were then used as instrumental variables in a multiple regression analysis (MR) to examine the effect of GM on the risk of PE within the IEU Open GWAS project, which included 2,118 PE cases and 359,076 controls. The principal analytical methodology utilized in this research was inverse variance weighting (IVW), complemented by assessments for pleiotropy and heterogeneity to confirm the results' resilience. The findings of this study are predominantly derived from the IVW method, providing evidence for causal associations between four distinct genera of GM and the risk of PE. Specifically, our analysis suggests that ( = 0.031), ( = 0.038), ( = 0.032), and ( = 0.049) may be linked to a decreased likelihood of developing PE. Importantly, our analysis yielded no evidence of heterogeneity or pleiotropy. In this MR study, we have established through genetic analysis that specific GM are significantly involved in the development of PE, underscoring the connection between the gut-lung axis and suggesting avenues for future research into the impact of GM on PE.
先前的研究表明,肠道微生物群(GM)失衡与肺部疾病之间存在联系,这表明肠道细菌可能通过“肠-肺”轴影响肺部健康。然而,GM与肺栓塞(PE)之间的直接联系尚不清楚。本研究采用孟德尔随机化研究来探究GM与PE的遗传关系。共有18340项独立的全基因组关联研究(GWAS)产生了与GM相关的单核苷酸多态性(SNP),这些SNP随后在IEU Open GWAS项目中被用作多元回归分析(MR)中的工具变量,该项目包括2118例PE病例和359076例对照。本研究中使用的主要分析方法是逆方差加权(IVW),并辅以多效性和异质性评估以确认结果的可靠性。本研究的结果主要来自IVW方法,为GM的四个不同属与PE风险之间的因果关联提供了证据。具体而言,我们的分析表明,[具体菌属1](P = 0.031)、[具体菌属2](P = 0.038)、[具体菌属3](P = 0.032)和[具体菌属4](P = 0.049)可能与发生PE的可能性降低有关。重要的是,我们的分析没有发现异质性或多效性的证据。在这项MR研究中,我们通过遗传分析确定了特定的GM在PE的发生中显著起作用,强调了肠-肺轴之间的联系,并为未来研究GM对PE的影响指明了方向。