Microbial modulation of cardiovascular disease

被引:353
作者
Brown, J. Mark [1 ]
Hazen, Stanley L. [1 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Cellular & Mol Med, 9500 Euclid Ave,NC-10, Cleveland, OH 44195 USA
关键词
TRIMETHYLAMINE-N-OXIDE; CONTAINING MONOOXYGENASE 3; PROTEIN-COUPLED RECEPTOR; VITAMIN-D-RECEPTOR; CHAIN FATTY-ACIDS; GUT MICROBIOTA; BILE-ACIDS; PORPHYROMONAS-GINGIVALIS; CHLAMYDIA-PNEUMONIAE; MORTALITY RISK;
D O I
10.1038/nrmicro.2017.149
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Although diet has long been known to contribute to the pathogenesis of cardiovascular disease (CVD), research over the past decade has revealed an unexpected interplay between nutrient intake, gut microbial metabolism and the host to modify the risk of developing CVD. Microbial-associated molecular patterns are sensed by host pattern recognition receptors and have been suggested to drive CVD pathogenesis. In addition, the host microbiota produces various metabolites, such as trimethylamine-N-oxide, short-chain fatty acids and secondary bile acids, that affect CVD pathogenesis. These recent advances support the notion that targeting the interactions between the host and microorganisms may hold promise for the prevention or treatment of CVD. In this Review, we summarize our current knowledge of the gut microbial mechanisms that drive CVD, with special emphasis on therapeutic interventions, and we highlight the need to establish causal links between microbial pathways and CVD pathogenesis.
引用
收藏
页码:171 / 181
页数:11
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