The potential of tailoring the gut microbiome to prevent and treat cardiometabolic disease

被引:38
|
作者
Chakaroun, Rima Mohsen [1 ,2 ]
Olsson, Lisa M. [1 ]
Backhed, Fredrik [1 ,3 ,4 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Med, Dept Mol & Clin Med,Wallenberg Lab, Gothenburg, Sweden
[2] Univ Leipzig, Med Ctr, Med Dept Endocrinol Nephrol Rheumatol 3, Leipzig, Germany
[3] Sahlgrens Univ Hosp, Dept Clin Physiol, Reg Vastra Gotaland, Gothenburg, Sweden
[4] Univ Copenhagen, Fac Hlth Sci, Novo Nordisk Fdn, Ctr Basic Metab Res, Copenhagen, Denmark
关键词
CHAIN FATTY-ACIDS; TRIMETHYLAMINE-N-OXIDE; INCIDENT CARDIOVASCULAR EVENTS; PROTEIN-COUPLED RECEPTOR; RANDOMIZED DOUBLE-BLIND; CORONARY-HEART-DISEASE; METABOLIC SYNDROME; INTESTINAL MICROBIOTA; BLOOD-PRESSURE; DIETARY FIBER;
D O I
10.1038/s41569-022-00771-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this Review, Backhed and colleagues summarize the evidence for gut microbiome alterations in cardiometabolic and cardiovascular diseases and the rationale and potential benefit motivating translational approaches to target the gut microbiota and its metabolites for prevention and treatment. Despite milestones in preventive measures and treatment, cardiovascular disease (CVD) remains associated with a high burden of morbidity and mortality. The protracted nature of the development and progression of CVD motivates the identification of early and complementary targets that might explain and alleviate any residual risk in treated patients. The gut microbiota has emerged as a sentinel between our inner milieu and outer environment and relays a modified risk associated with these factors to the host. Accordingly, numerous mechanistic studies in animal models support a causal role of the gut microbiome in CVD via specific microbial or shared microbiota-host metabolites and have identified converging mammalian targets for these signals. Similarly, large-scale cohort studies have repeatedly reported perturbations of the gut microbial community in CVD, supporting the translational potential of targeting this ecological niche, but the move from bench to bedside has not been smooth. In this Review, we provide an overview of the current evidence on the interconnectedness of the gut microbiome and CVD against the noisy backdrop of highly prevalent confounders in advanced CVD, such as increased metabolic burden and polypharmacy. We further aim to conceptualize the molecular mechanisms at the centre of these associations and identify actionable gut microbiome-based targets, while contextualizing the current knowledge within the clinical scenario and emphasizing the limitations of the field that need to be overcome.
引用
收藏
页码:217 / 235
页数:19
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