Heart Center & Beijing Key Laboratory of Hypertension, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Capital Medical University, Beijing, China.
mSphere. 2020 Mar 18;5(2):e00071-20. doi: 10.1128/mSphere.00071-20.
Dysbiotic gut microbiota (GM) and disordered metabolic patterns are known to be involved in the clinical expression of atrial fibrillation (AF). However, little evidence has been reported in characterizing the specific changes in fecal microbiota in paroxysmal AF (PAF) and persistent AF (psAF). To provide a comprehensive understanding of GM dysbiosis in AF types, we assessed the GM signatures of 30 PAF patients, 20 psAF patients, and 50 non-AF controls based on metagenomic and metabolomic analyses. Compared with control subjects, similar changes of GM were identified in PAF and psAF patients, with elevated microbial diversity and similar alteration in the microbiota composition. PAF and psAF patients shared the majority of differential taxa compared with non-AF controls. Moreover, the similarity was also illuminated in microbial function and associated metabolic alterations. Additionally, minor disparity was observed in PAF compared with psAF. Several distinctive taxa between PAF and psAF were correlated with certain metabolites and atrial diameter, which might play a role in the pathogenesis of atrial remodeling. Our findings characterized the presence of many common features in GM shared by PAF and psAF, which occurred at the self-terminating PAF. Preventative and therapeutic measures targeting GM for early intervention to postpone the progression of AF are highly warranted. Atrial fibrillation has been identified to be associated with disordered gut microbiota. Notably, atrial fibrillation is a progressive disease and could be categorized as paroxysmal and persistent based on the duration of the episodes. The persistent atrial fibrillation patients are accompanied by higher risk of stroke and lower success rate of rhythm control. However, the microbial signatures of different categories of atrial fibrillation patients remain unknown. We sought to determine whether disordered gut microbiota occurs in the self-terminating PAF or intestinal flora develops dynamically during atrial fibrillation progression. We found that different types of atrial fibrillation show a limited degree of gut microbiota shift. Gut microbiota dysbiosis has already occurred in mild stages of atrial fibrillation, which might act as an early modulator of disease, and therefore may be regarded as a potential target to postpone atrial fibrillation progression.
肠道微生物群落失调(GM)和代谢模式紊乱已被证实与心房颤动(AF)的临床表型有关。然而,关于阵发性 AF(PAF)和持续性 AF(psAF)患者粪便微生物群落的具体变化特征,目前报道甚少。为了全面了解 AF 类型中 GM 失调的情况,我们基于宏基因组和代谢组学分析,评估了 30 例 PAF 患者、20 例 psAF 患者和 50 例非 AF 对照者的 GM 特征。与对照组相比,PAF 和 psAF 患者的 GM 变化相似,微生物多样性升高,微生物群落组成也发生类似改变。与非 AF 对照组相比,PAF 和 psAF 患者具有大多数差异分类群。此外,在微生物功能和相关代谢改变方面也存在相似性。此外,与 psAF 相比,PAF 中也存在较小的差异。PAF 和 psAF 之间的一些独特分类群与某些代谢物和心房直径相关,这些代谢物和心房直径可能在心房重构的发病机制中发挥作用。我们的研究结果表明,PAF 和 psAF 患者 GM 存在许多共同特征,这些特征在自终止的 PAF 中存在。针对 GM 进行早期干预以延缓 AF 进展的预防和治疗措施是非常必要的。已经发现,肠道微生物群落失调与心房颤动有关。值得注意的是,心房颤动是一种进行性疾病,根据发作持续时间可以分为阵发性和持续性。持续性心房颤动患者中风风险较高,节律控制成功率较低。然而,不同类型心房颤动患者的微生物特征尚不清楚。我们试图确定在自终止的 PAF 中是否存在肠道菌群失调,或者在心房颤动进展过程中肠道菌群是否会发生动态变化。我们发现,不同类型的心房颤动显示出有限程度的肠道微生物群转移。肠道微生物群落失调已经在心房颤动的轻度阶段发生,这可能作为疾病的早期调节剂,因此可能被视为延缓心房颤动进展的潜在靶点。