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The gut microbiome in coronary artery disease and heart failure: Current knowledge and future directions

机译:冠状动脉疾病和心力衰竭的肠道微生物组:当前的知识和未来方向

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Host-microbiota interactions involving inflammatory and metabolic pathways have been linked to the pathogenesis of multiple immune-mediated diseases and metabolic conditions like diabetes and obesity. Accumulating evidence suggests that alterations in the gut microbiome could play a role in cardiovascular disease. This review focuses on recent advances in our understanding of the interplay between diet, gut microbiota and cardiovascular disease, with emphasis on heart failure and coronary artery disease. Whereas much of the literature has focused on the circulating levels of the diet- and microbiota-dependent metabolite trimethylamine-N-oxide (TMAO), several recent sequencing-based studies have demonstrated compositional and functional alterations in the gut microbiomes in both diseases. Some microbiota characteristics are consistent across several study cohorts, such as a decreased abundance of microbes with capacity for producing butyrate. However, the published gut microbiota studies generally lack essential covariates like diet and clinical data, are too small to capture the substantial variation in the gut microbiome, and lack parallel plasma samples, limiting the ability to translate the functional capacity of the gut microbiomes to actual function reflected by circulating microbiota-related metabolites. This review attempts to give directions for future studies in order to demonstrate clinical utility of the gut-heart axis.
机译:涉及炎症和代谢途径的宿主微生物A相互作用与多种免疫介导的疾病的发病机制和糖尿病等代谢条件相关联。累积证据表明,肠道微生物组的变化可以在心血管疾病中发挥作用。本综述重点是我们对饮食,肠道微生物群和心血管疾病之间相互作用的理解,重点是心力衰竭和冠状动脉疾病的最新进展。而大部分文献都集中在饮食和微生物纳依赖于代谢物三甲胺-N-氧化物(TMAO)的循环水平上,但最近的几种基于序列的研究已经证明了这两种疾病中的肠道微生物体中的组成和功能改变。一些微生物群特征在几种研究队列中一致,例如降低的微生物丰富的微生物,其具有生产丁酸酯的能力。然而,公布的肠道微生物群研究通常缺乏必要的协变量,如饮食和临床数据,太小,不能捕获肠道微生物组的大量变化,缺乏平行的血浆样品,限制了将肠道微生物血清功能的功能能力转化为实际的能力通过循环微生物群相关代谢物反映的功能。该审查试图向未来研究提供指示,以证明肠轴的临床效用。

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