Gut microbiota: a promising target against cardiometabolic diseases

被引:38
作者
Warmbrunn, Moritz, V [1 ]
Herrema, Hilde [2 ]
Aron-Wisnewsky, Judith [1 ,3 ,4 ]
Soeters, Maarten R. [5 ]
Van Raalte, Daniel H. [6 ,7 ]
Nieuwdorp, Max [1 ,2 ,5 ,6 ,7 ]
机构
[1] Univ Amsterdam, Dept Vasc Med, Amsterdam UMC, Locat AMC, Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Expt Vasc Med, Amsterdam UMC, Locat AMC, Amsterdam, Netherlands
[3] Sorbonne Univ, INSERM, Nutr & Obes Syst Approaches Nutri, Paris, France
[4] Hop La Pitie Salpetriere, AP HP, Nutr Dept, Paris, France
[5] Univ Amsterdam, Dept Endocrinol & Metab, Amsterdam UMC, Locat AMC, Amsterdam, Netherlands
[6] Vrije Univ Amsterdam, Diabet Ctr, Dept Internal Med, Amsterdam UMC,Locat VUMC, Amsterdam, Netherlands
[7] Vrije Univ Amsterdam, Amsterdam UMC, ICar, Amsterdam, Netherlands
关键词
Gut microbiome; cardiovascular diseases; metabolic diseases; inflammation; drug therapy; TRIMETHYLAMINE-N-OXIDE; CHAIN FATTY-ACIDS; FARNESOID X RECEPTOR; LOW-GRADE INFLAMMATION; BILE-ACID; INTESTINAL MICROBIOTA; CARDIOVASCULAR-DISEASE; INSULIN SENSITIVITY; METABOLIC SYNDROME; AKKERMANSIA-MUCINIPHILA;
D O I
10.1080/17446651.2020.1720511
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Cardiometabolic diseases (CMD) are a group of interrelated disorders such as metabolic syndrome, type 2 diabetes mellitus and cardiovascular diseases (CVD). As the prevalence of these diseases increases globally, efficient new strategies are necessary to target CMD and modifiable risk factors. In the past decade, evidence has accumulated regarding the influence of gut microbiota (GM) on CMD, providing new targets for therapeutic interventions. Areas covered: This narrative review discusses the pathophysiologic link between CMD, GM, and potential microbiota-based targets against atherosclerosis and modifiable risk factors for atherosclerosis. Low-grade inflammation can be induced through GM and its derived metabolites. CMD are influenced by GM and microbiota-derived metabolites such as short-chain fatty acids (SCFA), secondary bile acids, trimethylamine N-oxide (TMAO), and the composition of GM can modulate host metabolism. All of the above can lead to promising therapeutic targets. Expert opinion: Most data are derived from animal models or human association studies; therefore, more translational and interventional research in humans is necessary to validate these promising findings. Reproduced findings such as aberrant microbiota patterns or circulating biomarkers could be targeted depending on individual metabolic profiles, moving toward personalized medicine in CMD.
引用
收藏
页码:13 / 27
页数:15
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