Zhao Xinyue, Zhou Ruilin, Li Hanyu, Fan Yue, Sun Yueshen, Hu Xiaomin, Zhang Shuyang
State Key Laboratory of Complex Severe and Rare Diseases, Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China.
Department of Medical Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China.
Front Cardiovasc Med. 2021 Nov 2;8:767692. doi: 10.3389/fcvm.2021.767692. eCollection 2021.
Epidemiological studies confirmed that moderate alcohol consumption was associated with a reduced risk of adverse cardiovascular events. It is increasingly recognized that the composition of gut microbiota and metabolites is involved in modulating the cardiovascular health of the host. However, the association of moderate alcohol consumption with serum metabolites and gut microbiome and its impact on coronary artery disease (CAD) is not fully investigated. Serum untargeted metabolomics analysis and fecal 16S rRNA sequencing were performed on 72 male patients with CAD having various alcohol consumption (36 non-drinkers, 18 moderate drinkers, and 18 heavy drinkers) and 17 matched healthy controls. MetaboAnalyst and PICRUSt2 were utilized to analyze the possible involved metabolic pathways. Multi-omics analysis was achieved by Spearman correlation to reveal the interactions of alcohol consumption with gut microbiome and serum metabolites in patients with CAD. We noted distinct differences between patients with CAD, with varying levels of alcohol consumption and healthy controls in aspects of serum metabolome and the gut microbiome. Moderate alcohol consumption significantly changed the lipidomic profiles, including reductions of sphingolipids and glycerophospholipids in moderate drinkers with CAD when compared with non and heavy drinkers with CAD. Moreover, we also found the reduction of microbial-derived metabolites in moderate drinkers with CAD, such as 2-phenylacetamide and mevalonic acid. To be noted, the gut microbiota of moderate drinkers with CAD tended to resemble that of healthy controls. Compared with non-drinkers, the relative abundance of genus was significantly elevated in moderate drinkers with CAD, while the genus , and were significantly reduced in moderate drinkers with CAD. Multi-omics analysis revealed that specific metabolites and microbes associated with moderate alcohol consumption were correlated with the severity of CAD. Our study revealed that the impact of moderate alcohol consumption on serum metabolites and gut microbiota in patients with CAD seemed to be separated from that of heavy and non-alcohol consumption. Moderate drinking tended to have more positive effects on metabolic profiles and commensal flora, which may explain its beneficial effects on cardiovascular health. Overall, our study provides a novel insight into the effects of moderate alcohol consumption in patients with CAD.
流行病学研究证实,适度饮酒与不良心血管事件风险降低有关。人们越来越认识到,肠道微生物群及其代谢产物的组成参与调节宿主的心血管健康。然而,适度饮酒与血清代谢产物和肠道微生物群的关联及其对冠状动脉疾病(CAD)的影响尚未得到充分研究。对72名有不同饮酒量的男性CAD患者(36名不饮酒者、18名适度饮酒者和18名重度饮酒者)以及17名匹配的健康对照者进行了血清非靶向代谢组学分析和粪便16S rRNA测序。利用MetaboAnalyst和PICRUSt2分析可能涉及的代谢途径。通过Spearman相关性进行多组学分析,以揭示CAD患者饮酒与肠道微生物群和血清代谢产物之间的相互作用。我们注意到,在血清代谢组和肠道微生物群方面,不同饮酒水平的CAD患者与健康对照者之间存在明显差异。适度饮酒显著改变了脂质组学特征,与不饮酒和重度饮酒的CAD患者相比,适度饮酒的CAD患者中鞘脂和甘油磷脂减少。此外,我们还发现适度饮酒的CAD患者中微生物衍生代谢产物减少,如2-苯乙酰胺和甲羟戊酸。需要注意的是,适度饮酒的CAD患者的肠道微生物群倾向于与健康对照者相似。与不饮酒者相比,适度饮酒的CAD患者中属的相对丰度显著升高,而适度饮酒的CAD患者中属、和显著降低。多组学分析表明,与适度饮酒相关的特定代谢产物和微生物与CAD的严重程度相关。我们的研究表明,适度饮酒对CAD患者血清代谢产物和肠道微生物群的影响似乎与重度饮酒和不饮酒的影响不同。适度饮酒往往对代谢谱和共生菌群有更积极的影响,这可能解释了其对心血管健康的有益作用。总体而言,我们的研究为适度饮酒对CAD患者的影响提供了新的见解。