Department of Cardiovascular Surgery, Daping Hospital, Army Medical University, No.10 Changjiang Branch Road, Yuzhong District, Chongqing, 400042, China.
Department of Hepatobiliary and Pancreatic Tumor Center, Chongqing University Cancer Hospital, 181, Hanyu Road, Shapingba District, Chongqing, 400030, China.
BMC Pulm Med. 2024 May 14;24(1):235. doi: 10.1186/s12890-024-02877-2.
Emerging evidences have demonstrated that gut microbiota composition is associated with pulmonary arterial hypertension (PAH). However, the underlying causality between intestinal dysbiosis and PAH remains unresolved.
An analysis using the two-sample Mendelian randomization (MR) approach was conducted to examine the potential causal relationship between gut microbiota and PAH. To assess exposure data, genetic variants associated with 196 bacterial traits were extracted from the MiBioGen consortium, which included a sample size of 18,340 individuals. As for the outcomes, summary statistics for PAH were obtained from the NHGRI-EBI GWAS Catalog, which conducted a meta-analysis of four independent studies comprising a total of 11,744 samples. Causal effects were estimated employing various methods, including inverse variance weighted (IVW), MR-Egger, weighted median, weight mode and simple mode, with sensitivity analyses also being implemented with Cochran's Q test, MR-Egger intercept test, MR-PRESSO, leave-one-out analysis, and funnel plots.
Following false discovery rate (FDR) correction, the genetically predicted genus Eubacterium fissicatena group (odds ratio (OR) 1.471, 95% confidence interval (CI) 1.178-1.837, q = 0.076) exhibited a causal association with PAH. In addition, the genus LachnospiraceaeUCG004 (OR 1.511, 95% CI 1.048-2.177) and genus RuminococcaceaeUCG002 (OR 1.407, 95% CI 1.040-1.905) showed a suggestive increased risk of PAH, while genus Eubacterium eligens group (OR 0.563, 95% CI 0.344-0.922), genus Phascolarctobacterium (OR 0.692, 95% CI 0.487-0.982), genus Erysipelatoclostridium (OR 0.757, 95% CI 0.579-0.989) and genus T-yzzerella3 (OR 0.768, 95% CI 0.624-0.945) were found to have nominal protective effect against PAH.
The findings from our MR study have revealed a potential causal relationship between gut microbiota and PAH. Specifically, we have identified four types of gut microbiota that exhibit a protective effect on PAH, as well as three types that have a detrimental impact on PAH, thereby offering valuable insights for future mechanistic and clinical investigations in the field of PAH.
越来越多的证据表明,肠道微生物群组成与肺动脉高压(PAH)有关。然而,肠道失调与 PAH 之间的潜在因果关系仍未得到解决。
采用两样本孟德尔随机化(MR)分析方法,研究肠道微生物群与 PAH 之间的潜在因果关系。为了评估暴露数据,从包含 18340 个人的 MiBioGen 联盟中提取了与 196 种细菌特征相关的遗传变异。对于结局,从 NHGRI-EBI GWAS 目录中获得了 PAH 的汇总统计数据,该目录对四项独立研究进行了荟萃分析,共包含 11744 个样本。采用多种方法估计因果效应,包括逆方差加权(IVW)、MR-Egger、加权中位数、加权模式和简单模式,并通过 Cochran's Q 检验、MR-Egger 截距检验、MR-PRESSO、逐一剔除分析和漏斗图进行敏感性分析。
经过错误发现率(FDR)校正后,具有统计学意义的与 PAH 相关的细菌分类群为 Eubacterium fissicatena 组(比值比(OR)1.471,95%置信区间(CI)1.178-1.837,q=0.076)。此外,LachnospiraceaeUCG004 属(OR 1.511,95%CI 1.048-2.177)和 RuminococcaceaeUCG002 属(OR 1.407,95%CI 1.040-1.905)也显示出 PAH 的风险增加,而 Eubacterium eligens 组(OR 0.563,95%CI 0.344-0.922)、Phascolarctobacterium 属(OR 0.692,95%CI 0.487-0.982)、Erysipelatoclostridium 属(OR 0.757,95%CI 0.579-0.989)和 T-yzzerella3 属(OR 0.768,95%CI 0.624-0.945)与 PAH 呈负相关。
本 MR 研究结果表明肠道微生物群与 PAH 之间存在潜在的因果关系。具体而言,我们发现了四种对 PAH 具有保护作用的肠道微生物群,以及三种对 PAH 具有不利影响的肠道微生物群,为 PAH 领域的未来机制和临床研究提供了有价值的见解。