Departments of Medicine, Human Genetics, and Microbiology, Immunology, & Molecular Genetics, David Geffen School of Medicine of UCLA, Los Angeles, CA 90095, USA.
Department of Bacteriology, University of Wisconsin, Madison, Madison, WI 53706, USA.
Mol Metab. 2022 Oct;64:101557. doi: 10.1016/j.molmet.2022.101557. Epub 2022 Jul 21.
The gut microbiome influences host physiology and cardiometabolic diseases by interacting directly with intestinal cells or by producing molecules that enter the host circulation. Given the large number of microbial species present in the gut and the numerous factors that influence gut bacterial composition, it has been challenging to understand the underlying biological mechanisms that modulate risk of cardiometabolic disease.
Here we discuss a systems-based approach that involves simultaneously examining individuals in populations for gut microbiome composition, molecular traits using "omics" technologies, such as circulating metabolites quantified by mass spectrometry, and clinical traits. We summarize findings from landmark studies using this approach and discuss future applications.
Population-based integrative approaches have identified a large number of microbe-derived or microbe-modified metabolites that are associated with cardiometabolic traits. The knowledge gained from these studies provide new opportunities for understanding the mechanisms involved in gut microbiome-host interactions and may have potentially important implications for developing novel therapeutic approaches.
肠道微生物组通过与肠道细胞直接相互作用或产生进入宿主循环的分子来影响宿主生理学和心血管代谢疾病。鉴于肠道中存在大量的微生物物种,以及影响肠道细菌组成的众多因素,理解调节心血管代谢疾病风险的潜在生物学机制一直具有挑战性。
在这里,我们讨论了一种基于系统的方法,该方法涉及同时对人群中的个体进行肠道微生物组组成、使用“组学”技术(如通过质谱定量的循环代谢物)检测的分子特征以及临床特征的检查。我们总结了使用这种方法的标志性研究的结果,并讨论了未来的应用。
基于人群的综合方法已经确定了大量与心血管代谢特征相关的微生物衍生或微生物修饰的代谢物。这些研究获得的知识为理解肠道微生物组-宿主相互作用中涉及的机制提供了新的机会,并可能对开发新的治疗方法具有重要意义。