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靶向心血代谢风险的药物对肠道微生物群的影响。

Impact drugs targeting cardiometabolic risk on the gut microbiota.

机构信息

Department of Internal and Vascular Medicine, Amsterdam UMC, Location AMC, University of Amsterdam, Amsterdam.

Horaizon BV, Delft.

出版信息

Curr Opin Lipidol. 2021 Feb 1;32(1):38-54. doi: 10.1097/MOL.0000000000000727.

Abstract

PURPOSE OF REVIEW

Alterations in the gut microbiome composition or function are associated with risk factors for cardiometabolic diseases, including hypertension, hyperlipidemia and hyperglycemia. Based on recent evidence that also oral medications used to treat these conditions could alter the gut microbiome composition and function and, vice versa, that the gut microbiome could affect the efficacy of these treatments, we reviewed the literature on these observed interactions.

RECENT FINDINGS

While the interaction of metformin with the gut microbiome has been studied most, other drugs that target cardiometabolic risk are gaining attention and often showed associations with alterations in microbiome-related features, including alterations in specific microbial taxa or pathways, microbiome composition or microbiome-derived metabolites, while the gut microbiome was also involved in drug metabolism and drug efficacy. As for metformin, for some of them even a potential therapeutic effect via the gut microbiome is postulated. However, exact mechanisms remain to be elucidated.

SUMMARY

There is growing interest in clarifying the interactions between the gut microbiome and drugs to treat hypertension, hyperlipidemia and hyperglycemia as well as the first pass effect of microbiome on drug efficacy. While mostly analysed in animal models, also human studies are gaining more and more traction. Improving the understanding of the gut microbiome drug interaction can provide clinical directions for therapy by optimizing drug efficacy or providing new targets for drug development.

摘要

目的综述

肠道微生物组的组成或功能的改变与心血管代谢疾病的危险因素有关,包括高血压、高血脂和高血糖。基于最近的证据表明,用于治疗这些疾病的口服药物也可以改变肠道微生物组的组成和功能,反之亦然,肠道微生物组也可以影响这些治疗的效果,我们综述了关于这些观察到的相互作用的文献。

最近的发现

虽然二甲双胍与肠道微生物组的相互作用研究最多,但其他针对心血管代谢风险的药物也引起了关注,并且经常与微生物组相关特征的改变相关联,包括特定微生物类群或途径的改变、微生物组组成或微生物组衍生的代谢物,而肠道微生物组也参与药物代谢和药物疗效。对于二甲双胍,对于其中一些药物,甚至通过肠道微生物组来假设其潜在的治疗效果。然而,确切的机制仍有待阐明。

总结

人们越来越关注阐明肠道微生物组与治疗高血压、高血脂和高血糖的药物之间的相互作用以及微生物组对药物疗效的首过效应。虽然主要在动物模型中进行分析,但人类研究也越来越受到关注。通过优化药物疗效或为药物开发提供新的靶点,更好地理解肠道微生物组与药物的相互作用可以为治疗提供临床方向。

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