Ciccone Marco Matteo, Lepera Mario Erminio, Guaricci Andrea Igoren, Forleo Cinzia, Cafiero Concetta, Colella Marica, Palmirotta Raffele, Santacroce Luigi
Cardiology Unit, Interdisciplinary Department of Medicine, School of Medicine, University of Bari "Aldo Moro", 70124 Bari, Italy.
Area of Molecular Pathology, Anatomic Pathology Unit, Fabrizio Spaziani Hospital, 03100 Frosinone, Italy.
J Pers Med. 2023 Sep 7;13(9):1360. doi: 10.3390/jpm13091360.
In recent years, the increasing number of studies on the relationship between the gut microbiota and atherosclerosis have led to significant interest in this subject. The gut microbiota, its metabolites (metabolome), such as TMAO, and gut dysbiosis play an important role in the development of atherosclerosis. Furthermore, inflammation, originating from the intestinal tract, adds yet another mechanism by which the human ecosystem is disrupted, resulting in the manifestation of metabolic diseases and, by extension, cardiovascular diseases. The scientific community must understand and elucidate these mechanisms in depth, to gain a better understanding of the relationship between atherosclerosis and the gut microbiome and to promote the development of new therapeutic targets in the coming years. This review aims to present the knowledge acquired so far, to trigger others to further investigate this intriguing topic.
近年来,关于肠道微生物群与动脉粥样硬化之间关系的研究日益增多,引发了人们对该主题的浓厚兴趣。肠道微生物群、其代谢产物(代谢组),如氧化三甲胺(TMAO)以及肠道菌群失调在动脉粥样硬化的发展中起着重要作用。此外,源自肠道的炎症又增加了一种扰乱人体生态系统的机制,导致代谢性疾病的表现,并进而引发心血管疾病。科学界必须深入理解和阐明这些机制,以便更好地了解动脉粥样硬化与肠道微生物群之间的关系,并在未来推动新治疗靶点的开发。本综述旨在呈现目前已获得的知识,激发其他人进一步研究这一有趣的课题。