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血栓形成中的肠道微生物群

The gut microbiota in thrombosis.

作者信息

Khuu My Phung, Paeslack Nadja, Dremova Olga, Benakis Corinne, Kiouptsi Klytaimnistra, Reinhardt Christoph

机构信息

Center for Thrombosis and Hemostasis (CTH), University Medical Center Mainz, Johannes Gutenberg-University Mainz, Mainz, Germany.

Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Munich, Germany.

出版信息

Nat Rev Cardiol. 2025 Feb;22(2):121-137. doi: 10.1038/s41569-024-01070-6. Epub 2024 Sep 17.

DOI:10.1038/s41569-024-01070-6
PMID:39289543
Abstract

The gut microbiota has emerged as an environmental risk factor that affects thrombotic phenotypes in several cardiovascular diseases. Evidence includes the identification of marker species by sequencing studies of the gut microbiomes of patients with thrombotic disease, the influence of antithrombotic therapies on gut microbial diversity, and preclinical studies in mouse models of thrombosis that have demonstrated the functional effects of the gut microbiota on vascular inflammatory phenotypes and thrombus formation. In addition to impaired gut barrier function promoting low-grade inflammation, gut microbiota-derived metabolites have been shown to act on vascular cell types and promote thrombus formation. Therefore, these meta-organismal pathways that link the metabolic capacities of gut microorganisms with host immune functions have emerged as potential diagnostic markers and novel drug targets. In this Review, we discuss the link between the gut microbiota, its metabolites and thromboembolic diseases.

摘要

肠道微生物群已成为一种环境风险因素,影响多种心血管疾病的血栓形成表型。证据包括通过对血栓形成疾病患者的肠道微生物群进行测序研究来鉴定标记物种、抗血栓治疗对肠道微生物多样性的影响,以及血栓形成小鼠模型的临床前研究,这些研究证明了肠道微生物群对血管炎症表型和血栓形成的功能作用。除了受损的肠道屏障功能会促进低度炎症外,肠道微生物群衍生的代谢产物已被证明可作用于血管细胞类型并促进血栓形成。因此,这些将肠道微生物的代谢能力与宿主免疫功能联系起来的元生物体途径已成为潜在的诊断标志物和新型药物靶点。在本综述中,我们讨论了肠道微生物群及其代谢产物与血栓栓塞性疾病之间的联系。

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本文引用的文献

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Gut microbial co-metabolite 2-methylbutyrylcarnitine exacerbates thrombosis via binding to and activating integrin α2β1.肠道微生物共代谢物 2-甲基丁酰肉碱通过与整合素 α2β1 结合并激活其来加重血栓形成。
Cell Metab. 2024 Mar 5;36(3):598-616.e9. doi: 10.1016/j.cmet.2024.01.014. Epub 2024 Feb 23.
2
Microbial-derived imidazole propionate links the heart failure-associated microbiome alterations to disease severity.微生物衍生的咪唑丙酸将与心力衰竭相关的微生物组改变与疾病严重程度联系起来。
Genome Med. 2024 Feb 8;16(1):27. doi: 10.1186/s13073-024-01296-6.
3
Gut complement induced by the microbiota combats pathogens and spares commensals.
一种用于连续粒子和细胞操控的无泵液压放大振荡微流控装置。
Adv Sci (Weinh). 2025 Aug;12(30):e07041. doi: 10.1002/advs.202507041. Epub 2025 May 23.
4
The Critical Role of in Cardiovascular Diseases.(原文中“in Cardiovascular Diseases”前缺少具体内容,推测可能是某个因素之类的,这里仅按现有内容翻译)……在心血管疾病中的关键作用。
Rev Cardiovasc Med. 2025 Mar 20;26(3):26740. doi: 10.31083/RCM26740. eCollection 2025 Mar.
5
Gut microbiota and derived metabolites mediate obstructive sleep apnea induced atherosclerosis.肠道微生物群及其衍生代谢产物介导阻塞性睡眠呼吸暂停诱发的动脉粥样硬化。
Gut Microbes. 2025 Dec;17(1):2474142. doi: 10.1080/19490976.2025.2474142. Epub 2025 Mar 2.
6
Gut microbiome and inflammation in cardiovascular drug response: trends in therapeutic success and commercial focus.肠道微生物群与心血管药物反应中的炎症:治疗成功趋势与商业焦点
Inflammopharmacology. 2025 Jan;33(1):49-68. doi: 10.1007/s10787-024-01593-x. Epub 2024 Nov 2.
肠道菌群诱导的补体系统既能抵御病原体,又能与共生菌共存。
Cell. 2024 Feb 15;187(4):897-913.e18. doi: 10.1016/j.cell.2023.12.036. Epub 2024 Jan 26.
4
Sterility testing of germ-free mouse colonies.无菌鼠群的无菌检测。
Front Immunol. 2023 Nov 7;14:1275109. doi: 10.3389/fimmu.2023.1275109. eCollection 2023.
5
Microbe-derived uremic solutes enhance thrombosis potential in the host.微生物来源的尿毒症溶质增强宿主的血栓形成潜力。
mBio. 2023 Dec 19;14(6):e0133123. doi: 10.1128/mbio.01331-23. Epub 2023 Nov 10.
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Gut microbiota aggravates neutrophil extracellular traps-induced pancreatic injury in hypertriglyceridemic pancreatitis.肠道微生物群加剧了高脂血症性胰腺炎中中性粒细胞胞外诱捕网诱导的胰腺损伤。
Nat Commun. 2023 Oct 4;14(1):6179. doi: 10.1038/s41467-023-41950-y.
7
Mechanism-based inhibition of gut microbial tryptophanases reduces serum indoxyl sulfate.基于机制的肠道微生物色氨酸酶抑制作用可降低血清吲哚硫酸酯。
Cell Chem Biol. 2023 Nov 16;30(11):1402-1413.e7. doi: 10.1016/j.chembiol.2023.07.015. Epub 2023 Aug 25.
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Trimethylamine N-Oxide and White Matter Hyperintensity Volume Among Patients With Acute Ischemic Stroke.三甲胺氮氧化物与急性缺血性脑卒中患者的脑白质高信号体积。
JAMA Netw Open. 2023 Aug 1;6(8):e2330446. doi: 10.1001/jamanetworkopen.2023.30446.
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