Interactions Between Therapeutics for Metabolic Disease, Cardiovascular Risk Factors, and Gut Microbiota

被引:23
作者
Ding, Qi-You [1 ,2 ]
Tian, Jia-Xing [1 ]
Li, Min [1 ]
Lian, Feng-Mei [1 ]
Zhao, Lin-Hua [1 ]
Wei, Xiu-Xiu [1 ,2 ]
Han, Lin [1 ]
Zheng, Yu-Jiao [1 ,2 ]
Gao, Ze-Zheng [1 ,2 ]
Yang, Hao-Yu [1 ,2 ]
Fang, Xin-Yi [1 ,2 ]
Tong, Xiao-lin [1 ]
机构
[1] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Endocrinol, Beijing, Peoples R China
[2] Beijing Univ Tradit Chinese Med, Grad Coll, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
metabolic therapy; gut microbiota; cardiovascular diseases; metformin; microbiota-targeted therapies; CORONARY-HEART-DISEASE; CHAIN FATTY-ACIDS; IMPAIRED GLUCOSE-TOLERANCE; ALL-CAUSE MORTALITY; AKKERMANSIA-MUCINIPHILA; INTESTINAL MICROBIOTA; ACARBOSE TREATMENT; RECEPTOR AGONISTS; DIABETES-MELLITUS; OXIDATIVE STRESS;
D O I
10.3389/fcimb.2020.530160
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
With improved standards of living, the incidence of multiple metabolic disorders has increased year by year, especially major risk factors for cardiovascular disease such as hyperglycemia and hyperlipidemia, continues to increase. Emerging epidemiological data and clinical trials have shown the additional protective effects of some metabolic therapy drugs against cardiovascular diseases. A series of studies have found that these drugs may work by modulating the composition of gut microbiota. In this review, we provide a brief overview of the contribution of the gut microbiota to both metabolic disorders and cardiovascular diseases, as well as the response of gut microbiota to metabolic therapy drugs with cardiovascular benefits. In this manner, we link the recent advances in microbiome studies on metabolic treatment drugs with their cardiovascular protective effects, suggesting that intestinal microorganisms may play a potential role in reducing cardiovascular risk factors. We also discuss the potential of microorganism-targeted therapeutics as treatment strategies for preventing and/or treating cardiovascular disease and highlight the need to establish causal links between therapeutics for metabolic diseases, gut microbiota modulation, and cardiovascular protection.
引用
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页数:14
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