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首页> 外文期刊>Journal of atherosclerosis and thrombosis. >Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease
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Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease

机译:冠状动脉疾病患者肠道菌群的分析:肠道菌群与冠状动脉疾病之间的可能联系

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Aim : Recent studies have suggested that metabolic disorders such as obesity and type 2 diabetes are associated with gut microbiota. The association between atherosclerosis and gut microbiota has also been attracting increased attention. Our aim was to specify a characteristic trend of gut microbiota in coronary artery disease (CAD). Methods : This study included 39 CAD patients, 30 age- and sex-matched no-CAD controls (Ctrls) with coronary risk factors and 50 healthy volunteers (HVs) without coronary risk factors. Bacterial DNA was extracted from their fecal samples and analyzed by terminal restriction fragment length polymorphism. Results : A characteristic change of gut microbiota was observed in CAD patients, where the order Lactobacillales was increased (CAD, Ctrl vs. HV; 13.6%±12.0%, 6.2%±7.7% vs. 4.1%±5.9%; p <0.001) and the phylum Bacteroidetes ( Bacteroides + Prevotella ) was decreased (CAD, Ctrl vs. HV;35.5%±11.6%, 43.9%±11.2% vs. 47.4%±11.5%; p <0.001). The CAD group was over-represented in enterotype “others” (III), compared with the Ctrl or HV group ( p <0.001, chi-squared test), although we could not deny the possibility that some drugs affect the gut flora types. Conclusions : Although this study had some limitations, we demonstrated that the incidence of CAD was linked with an alteration of gut microbiota. A prospective study is desired to clarify a causal relationship between CAD and gut microbiota.
机译:目的:最近的研究表明,肥胖和2型糖尿病等代谢紊乱与肠道菌群有关。动脉粥样硬化与肠道菌群之间的关联也引起了越来越多的关注。我们的目的是确定冠状动脉疾病(CAD)中肠道菌群的特征性趋势。方法:本研究包括39例CAD患者,30例年龄和性别匹配的有冠心病危险因素的无CAD对照(Ctrls)和50例无冠心病危险因素的健康志愿者(HVs)。从它们的粪便样品中提取细菌DNA,并通过末端限制性片段长度多态性进行分析。结果:在CAD患者中观察到肠道菌群的特征性变化,其中乳杆菌的顺序增加(CAD,Ctrl vs. HV; 13.6%±12.0%,6.2%±7.7%vs. 4.1%±5.9%; p <0.001 )和拟杆菌门(拟杆菌+小菜蛾)减少(CAD,Ctrl vs.HV; 35.5%±11.6%,43.9%±11.2%vs.47.4%±11.5%; p <0.001)。尽管我们不能否认某些药物影响肠道菌群类型的可能性,但与Ctrl或HV组相比,CAD组在肠型“其他”(III)中的代表过多(p <0.001,卡方检验)。结论:尽管这项研究有一定的局限性,但我们证明了CAD的发生与肠道菌群的改变有关。希望进行前瞻性研究来阐明CAD与肠道菌群之间的因果关系。

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