State Key Laboratory of Organ Failure Research, Department of Cardiology, Nanfang Hospital, Southern Medical University, Guangzhou, China; Key Laboratory for Organ Failure Research, Ministry of Education of the People's Republic of China, Guangzhou, China.
State Key Laboratory of Organ Failure Research, Division of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Atherosclerosis. 2019 May;284:121-128. doi: 10.1016/j.atherosclerosis.2018.11.038. Epub 2018 Dec 4.
Although most risk factors for cardiac valve calcification (VC) are similar to those for coronary artery disease (CAD), they differ regarding lesions and clinical symptoms. Recently, increasing evidence suggests that intestinal bacteria play essential roles in cardiovascular disease (CVD). It is plausible that the gut microbiota is linked to the occurrence of different CVDs under similar risk factors. Thus, we aimed to explore the gut microbiomes in patients with VC or CAD and determine their underlying connections.
We collected samples from 119 subjects and performed 16S rRNA gene sequencing to analyze the gut microbiomes in VC and CAD patients and in control volunteers.
The gut microbiomes of VC and CAD patients were significantly different in terms of beta-diversity. Bacteria from Veillonella dispar, Bacteroides plebeius and Fusobacterium were enriched in the VC group, while members of Collinsella aerofaciens, Megamonas, Enterococcus, Megasphaera, Dorea and Blautia were decreased. According to the association with dyslipidemia, seven operational taxonomic units (OTUs), including Parabacteroides distasonis, Megamonas, Fusobacterium, Bacteroides sp., Bacteroides plebeius, Lactobacillus and Prevotella copri, were regarded as potential pathogens for CVDs. Additionally, Prevotella copri might be a keystone of CVDs, especially in VC patients, while Collinsella aerofaciens is a possible keystone of CAD, based on the multi-correlations of these bacteria with other OTUs in microbial communities.
Patients with VC and CAD suffer from different gut microbial dysbiosis. The gut microbiomes are associated with the clinical characteristics in these diseases and might be potential therapeutic targets.
尽管心脏瓣膜钙化(VC)的大多数风险因素与冠状动脉疾病(CAD)相似,但它们在病变和临床症状方面有所不同。最近,越来越多的证据表明,肠道细菌在心血管疾病(CVD)中起着至关重要的作用。肠道微生物群可能与相似风险因素下不同 CVD 的发生有关。因此,我们旨在探索 VC 或 CAD 患者的肠道微生物群,并确定它们的潜在联系。
我们收集了 119 名受试者的样本,并进行了 16S rRNA 基因测序,以分析 VC 和 CAD 患者以及对照志愿者的肠道微生物群。
VC 和 CAD 患者的肠道微生物群在β多样性方面存在显著差异。迪斯帕氏韦荣球菌、普通拟杆菌和梭菌在 VC 组中富集,而 Aeriscardovia aerofaciens、Megamonas、肠球菌、Megasphaera、多雷氏菌和 Blautia 减少。根据与血脂异常的关联,七个操作分类单元(OTUs),包括拟杆菌、Megamonas、梭菌、拟杆菌属、普通拟杆菌、乳杆菌和普雷沃氏菌,被认为是 CVD 的潜在病原体。此外,基于这些细菌与微生物群落中其他 OTUs 的多相关性,普雷沃氏菌可能是 CVD 的关键菌,特别是在 VC 患者中,而 Aeriscardovia aerofaciens 可能是 CAD 的关键菌。
VC 和 CAD 患者患有不同的肠道微生物失调。肠道微生物群与这些疾病的临床特征相关,可能是潜在的治疗靶点。