Spehlmann Martina E, Rangrez Ashraf Y, Dhotre Dhiraj P, Schmiedel Nesrin, Chavan Nikita, Bang Corinna, Müller Oliver J, Shouche Yogesh S, Franke Andre, Frank Derk, Frey Norbert
Department of Internal Medicine III, Cardiology, Angiology and Intensive Care Medicine, University Hospital of Schleswig-Holstein, Rosalind-Franklin Str. 12, 24105 Kiel, Germany.
German Centre for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, 24105 Kiel, Germany.
Biomedicines. 2022 Mar 30;10(4):809. doi: 10.3390/biomedicines10040809.
Growing evidence suggests an altered gut microbiome in patients with heart failure (HF). However, the exact interrelationship between microbiota, HF, and its consequences on the metabolome are still unknown. We thus aimed here to decipher the association between the severity and progression of HF and the gut microbiome composition and circulating metabolites. Using a mouse model of transverse aortic constriction (TAC), gut bacterial diversity was found to be significantly lower in mice as early as day 7 post-TAC compared to Sham controls (p = 0.03), with a gradual progressive decrease in alpha-diversity on days 7, 14, and 42 (p = 0.014, p = 0.0016, p = 0.0021) compared to day 0, which coincided with compensated hypertrophy, maladaptive hypertrophy, and overtly failing hearts, respectively. Strikingly, segregated analysis based on the severity of the cardiac dysfunction (EF < 40% vs. EF 40−55%) manifested marked differences in the abundance and the grouping of several taxa. Multivariate analysis of plasma metabolites and bacterial diversity produced a strong correlation of metabolic alterations, such as reduced short-chain fatty acids and an increase in primary bile acids, with a differential abundance of distinct bacteria in HF. In conclusion, we showed that HF begets HF, likely via a vicious cycle of an altered microbiome and metabolic products.
越来越多的证据表明,心力衰竭(HF)患者的肠道微生物群发生了改变。然而,微生物群、HF及其对代谢组的影响之间的确切相互关系仍不清楚。因此,我们旨在阐明HF的严重程度和进展与肠道微生物群组成及循环代谢物之间的关联。使用横向主动脉缩窄(TAC)小鼠模型,发现与假手术对照组相比,早在TAC术后第7天,小鼠的肠道细菌多样性就显著降低(p = 0.03),与第0天相比,在第7、14和42天α多样性逐渐下降(p = 0.014、p = 0.0016、p = 0.0021),这分别与代偿性肥大、适应性不良肥大和明显衰竭的心脏相一致。引人注目的是,基于心脏功能障碍严重程度(射血分数<40%与射血分数40 - 55%)的分类分析显示,几个分类群的丰度和分组存在显著差异。血浆代谢物和细菌多样性的多变量分析表明,代谢改变之间存在很强的相关性,如短链脂肪酸减少和初级胆汁酸增加,这与HF中不同细菌的差异丰度有关。总之,我们表明HF会导致HF,可能是通过微生物群和代谢产物改变的恶性循环。